Abstract
COVID‐19 had a great impact on medical approaches among dermatologist. This systematic review focuses on all skin problems related to COVID‐19, including primary and secondary COVID‐related cutaneous presentations and the experts recommendations about dermatological managements especially immunomodulators usage issues. Search was performed on PubMed, Scopus, Embase and ScienceDirect. Other additional resources were searched included Cochrane, WHO, Medscape and coronavirus dermatology resource of Nottingham university. The search completed on May 3, 2020. Three hundred seventy‐seven articles assigned to the inclusion and exclusion groups. Eighty‐nine articles entered the review. Primary mucocutaneous and appendageal presentations could be the initial or evolving signs of COVID‐19. It could be manifest most commonly as a maculopapular exanthamatous or morbiliform eruption, generalized urticaria or pseudo chilblains recognized as “COVID toes” (pernio‐like acral lesions or vasculopathic rashes). During pandemic, Non‐infected non‐at risk patients with immune‐medicated dermatologic disorders under treatment with immunosuppressive immunomodulators do not need to alter their regimen or discontinue their therapies. At‐risk o suspected patients may need dose reduction, interval increase or temporary drug discontinuation (at least 2 weeks). Patients with an active COVID‐19 infection should hold the biologic or non‐biologic immunosuppressives until the complete recovery occur (at least 4 weeks).
Keywords: alopecia, biologic, collagen vascular disorder, corona virus, cosmetic procedure, COVID‐19, cutaneous, cutaneous manifestation, dermatitis, dermatology, drug reaction, eczema, health care staff, hidradenitis suppurativa, immunobullous, immunomodulator, immunosupressant, immunosupressive, novel human coronavirus (SARS‐CoV‐2), pandemic considerations, papulosquamous, pemphigus, psoriasis, recommendation, skin, skin manifestation, skin rheumatologic disorder, special, specific skin diseases, surgical procedure, systematic review, systemic treatment, teledermatology, visits
Abbreviations
- CEBD
Centre of Evidence Based Dermatology
- COVID‐19
“CO” stands for corona, “VI” for virus, “D” for disease, and “19” for 2019
- PPE
Personal protective equipment
1. INTRODUCTION
COVID‐19 outbreak, globally, had a significant impact on the medical approaches among different specialties. For the dermatologist specifically, the cutaneous manifestations which are suggesting clues of COVID‐19 are of great importance. Several articles have been introduced patients with primary nail, mucosal and skin complaints as an initial or evolving presenting signs of COVID‐19. Maculopapular eruptions, urticaria, or the acral vasculopathic rashes (pseudo chilblains, pernio‐like lesions) recognized as the “COVID toe,” are the most common mucocutaneous manifestations of new corona virus; while the patients usually develop the common symptoms of COVID‐19, few days after the initiation of these skin eruptions. 1
There is also dermatoses like COVID‐19 treatment‐related drug reactions, especially the generalized pustular rash due to hydroxychloroquine. 2 In addition to mentioned dermatoses, there are many other dermatological concerns during pandemic as there are several skin conditions that may be treated by anti‐inflammatory, Immunomodulatory drugs or biologic agents, from them, vesiculobullous disease, autoimmune disorders, collagen vascular disease, psoriasis and so forth, could be mentioned and patients with these type of diseases considered as immunocompromised. 3 These patients may need drug‐dosage or drug‐administration frequency alterations or even drug cessations during the time of pandemic especially in the case of personal infection or having a highly suspicious exposure that may leading to further disease aggravation or poorly disease controlling. 4
Secondary dermatoses are other concerns in the pandemic, so occurrence of an acute new dermatose could be seen frequently; some due to stress‐related causes such as Herpes Simplex, Herpes Zoster, patchy alopecia areata and some due to physical‐environmental causes like acute allergic or irritant contact dermatitis or acute urticaria. 5
Moreover, some acute conditions have a tendency to become chronic, from these, telogen‐effluvium, eczema, chronic contact dermatitis, neurocutaneous or psychocutaneous disorders could be noted. There are also many preexisting chronic dermatoses may become poorly‐controlled or aggravated due to some circumstances (like stress, irregular visits, treatment interruptions, delayed therapies, physical, environmental and behavioral issues such as wearing masks and latex gloves, frequent washing and disinfectants, excessive sweating…) for example, rosacea, acne, dermatitis and systemic or non‐systemic immune‐mediated cutaneous disorders (immune‐bullous disorders, rheumatologic skin diseases, psoriasis, hidradenitis suppurativa, alopecia areata, lichen planus, and etc.). COVID‐19 pandemic highlighted the role of preventive measures while visiting the patients. In a study of United States, it have been reported that almost half of the dermatologist closed their office or limited their practices only to the patients needed emergency cares and the cosmetic or elective surgical procedures have been postponed. 6
This raises the urgent need for having a better knowledge about future perspectives in dermatology; considering teledermatology and try to know more about virus or its drug‐associated skin eruptions. 7
The aim of this systematic review is to present an overview of suggestive skin manifestations of the COVID‐19 and to address several considerations in the dermatological issues practices, during this pandemic.
2. METHOD
2.1. Protocol and registration
This study is implemented according to the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta‐Analyses) statement.
2.2. Eligibility criteria
Inclusion criteria comprised all studies about virus or drug‐related cutaneous manifestations of COVID‐19 and most presented concerns in the management of dermatologic disorders or patients may treat with immunosuppressive, immunomodulator and biologic therapies, acute presentation or aggravation of pre‐existing dermatoses like severe contact dermatitis, more severe atopic eczema, acute urticaria and etc, cutaneous adverse drug reactions, cutaneous involvements of health care providers and skin care issues; in this global pandemic. The exclusion criteria consisted of all publications not meeting the above, non‐English literature, studies before December 1, 2019 and studies in which no mention of skin manifestations of COVID‐19 or dermatology consideration in n‐cov2019 pandemic. Three hundred seventy‐seven articles assigned to the inclusion and exclusion groups. And after screening, 89 articles entered this systematic review as you see in Figure S1.
2.3. Information sources
Databases PubMed (http://ncbi.nlm.nih.gov/pubmed), Scopus (http://www.scopus.com), Embase (http://www.embase.com) and Sciencedirect (https://www.sciencedirect.com) have been searched for the evidence. Other sources searched to make use of the additional research were Cochrane (https://www.cochranelibrary.com/), WHO (http://www.who.int/emergencies/diseases/novel-coronavirus-2019), Medscape and CEBD coronavirus dermatology resource of Nottingham university (https://www.nottingham.ac.uk/).
2.4. Search strategy
Table S6 shows the search strategies used, not limit the entries to any condition. The search was performed by keywords COVID‐19 and alternative names has been called, and skin manifestations, dermatology considerations, skin care and their synonyms. The search completed on May 3, 2020, and only the articles after date of December 1, 2019 have been included.
2.5. Study selection
Endnote X8 (Clarivate Analytics, Philadelphia) was used for study screening and data extraction. 377 articles assigned to the inclusion and exclusion groups. In first step the titles and abstracts of articles were read. And, if accepted has evaluated to second step; the full‐text screening, the authors read the full‐text and executed the final inclusion articles. Disagreement situations regarding the inclusion process resolved through dialogue and no necessity for a third‐party involvement occurred.
3. RESULT
Totally there were 453 articles with 76 duplicate data that were deleted. Three hundred seventy‐seven articles were screened by the authors. From 377 articles, 240 article met exclusion criteria in the first step. And, 39 article met exclusion criteria in the second step. Eighty‐nine articles met inclusion criteria. Twenty‐seven articles were about cutaneous manifestation of COVID‐19; from them, 19 articles were case‐reports and 8 articles were case‐series. You can see the details in Figure S1. In Tables 1 and 2, we summarized case reports and case series of primary cutaneous COVID‐19‐related reactions, respectively. In Table 3, you can see cutaneous drug reactions related to COVID‐19 treatment, till to our systematic search. Since there are wide categories of proposed drugs for treatment of COVID‐19, In Table S8 the most prevalent and important cutaneous adverse reactions of these drugs is visible according to Tursen et al. review on all possible COVID‐19 drugs skin reaction. 44 Totally five articles were about skin drug reactions of COVID‐19 treatments; two of them were original studies as case reports that were summarized in Table S7. Also, in Sharma, Ajay et al and Jakhar et al. Studies, adverse effect of hydroxychloroquine were reviewed. 2 , 45 Eleven articles were about skin injuries among medical staff fighting COVID‐19 & general population and usable recommendation about skin care in this global crisis that summarized in Table 3. And in Table 4, prevalence of areas affected by secondary skin complications were recorded. Also, 46 articles were about concerns in management of immune‐based dermatologic disorders and autoimmune rheumatologic disorder and collagen vascular disease, and immunomodulator treatments in this pandemic. Twenty‐six of them do not have certain usable recommendation and 20 of them had specific advice that reported in Table 5. Table S6 shows our exact search strategy.
TABLE 1.
First author | Title | Cutaneous manifestation | Case characteristic | Accompanied by COVID‐19 symptoms | Drug history | Involvement site | Skin biopsy | Duration of skin lesion |
---|---|---|---|---|---|---|---|---|
Andrea Estébanez | Cutaneous manifestations in COVID‐19: a new contribution 8 | Pruritic erythematous‐yellowish papules | 28‐year‐old woman | 15 days after COVID‐19 diagnose | 10 days after last dose of paracetamol | On both heels | Not reported | Not reported |
Henry, D | Urticarial eruption in COVID‐19 infection 9 | Pruritic disseminated erythematous plaques eruption | 27‐year‐old woman | Before fever and respiratory syndrome | Not reported | Particular face and acral involvement | Not reported | Not reported |
B. ahouach | Cutaneous lesions in a patient with COVID‐19: are they related? 10 | Rash (Diffuse fixed erythematous blanching maculopapular lesions) | 57‐year‐old woman | 2 days after fever and in same time with dry cough | Not reported | Limbs and trunk and palms | Slight spongiosis, basal cell vacuolation and mild perivascular lymphocytic infiltrate | Not reported |
Anwar Alramthan |
A case of COVID‐19 presenting in clinical picture resembling chilblains disease. First report from the Middle East 11 |
Rash (red‐purple papules) | A 27‐year‐old females | Asymptotic, RT‐PCR confirmed COVID‐19 | Not reported | Acral areas (dorsal aspect of fingers bilaterally) | Not reported | Not reported |
Rash (red‐purple papules) + diffused erythema | 35‐year‐old female + subungual area of the right thumb | asymptotic RT‐PCR confirmed COVID‐19 | Not reported | Acral areas (dorsal aspect of fingers bilaterally) | Not reported | Not reported | ||
Nerea landa | Chilblain‐like lesions on feet and hands during the COVID‐19 Pandemic 12 | Reddish and papular resembling chilblains after 1 week they become more purpuric and flattened (referred discomfort or pain when palpated) | 15 year old male | Same time with chest x‐ray showing mild bilateral pneumonia | Not reported | Five in toes and heels | Not reported | Not reported |
23 year old female | 3 weeks after COVID‐19 symptoms | Not reported | Toes (were a little itchy) | Not reported | Not reported | |||
44 year old male | 10 days after COVID‐19 symptoms | Not reported | Toe (slightly painful) | Not reported | Not reported | |||
91 year old male | 3 weeks after COVID‐19 confirmed by PCR | Not reported | Toe | Not reported | Not reported | |||
24 year old female | after COVID‐19 confirmed by PCR | Not reported | Toes | Not reported | Not reported | |||
15 year old female | 1 week after COVID‐19 symptoms | Not reported | Fingers and heels (mildly painful when pressing) | Not reported | Not reported | |||
Wu, Ping | A child confirmed COVID‐19 with only symptoms of conjunctivitis and eyelid dermatitis 13 | Dermatitis | 2 years and 10 months old | 7 days after RT‐PCR confirmed COVID‐19 | Not reported | Eyelid | Not reported | 5 days |
Sachdeva, Muskaan | Cutaneous manifestations of COVID‐19: Report of three cases and a review of literature 14 | Maculo‐papular rash | 71‐year‐old Caucasian woman | 10 dayes after COVID‐19 symptomes | No medication | Trunk (itchy) | Not reported | Not reported |
Diffuse maculopapular exanthem (morbilliform) + macular hemorrhagic rash | 77‐year‐old Caucasian woman | At the same time with COVID‐19 symptoms | Not reported | Trunk + legs | Not reported | Not reported | ||
Papular‐vesicular, pruritic eruption | 72‐year‐old Caucasian woman | 4 days After COVID‐19 symptoms | Not reported | Sub‐mammary folds, trunk and hips | Not reported | Not reported | ||
Rivera‐Oyola, Ryan | Dermatologic findings in two patients with COVID‐19 15 | Rash and scattered erythematous macules coalescing into papules | 60‐year‐old male | 3 days after COVID‐19 symptoms | no recent changes to her medications | Back, flanks, groin and upper thighs | Mild perivascular infiltrate of predominantly mononuclear cells surrounding the superficial blood vessels and epidermis showed scattered foci of hydropic changes along with minimal acanthosis, slight spongiosis and foci of parakeratosis | 7 days |
Mild hemi‐facial atrophy and scoliosis, generalized, pruritic rash, large, disseminated, urticarial plaques | 60‐year‐old woman | 9 days after COVID‐19 symptoms | no recent changes to her medications | Trunk, head, upper and lower extremities | Not reported | 1 day | ||
Manalo, Iviensan F. | A Dermatologic Manifestation of COVID‐19: Transient Livedo Reticularis 16 | transient non‐pruritic blanching unilateral livedoid patch | 67‐year‐old Caucasian male | 7 days after COVID‐19 symptoms | Not reported | Right anterior thigh | Not reported | 1 day |
Unilateral asymptomatic rash | 47‐year‐old Caucasian female | 10 days after RT‐PCR confirmed COVID‐19 | Not reported | Right leg | Not reported | 1 day | ||
Mahé, A. | A distinctive skin rash associated with Coronavirus Disease 2019? 17 | Erythematous rash | 64 years old woman | 4 days after COVID‐19 symptoms | 4 days after began to take oral paracetamol | Both antecubital fossa, extended on the trunk and axillary folds | Not reported | 5 days |
Lu, S. | Alert for non‐respiratory symptoms of Coronavirus Disease 2019 (COVID‐19) patients in epidemic period: A case report of familial cluster with three asymptomatic COVID‐19 patients 18 | Generalized Urticaria | Not reported | 1 week after dry cough | Not reported | Generalized | Not reported | Not reported |
Hunt, M. | A Case of COVID‐19 Pneumonia in a Young Male with Full Body Rash as a Presenting Symptom 19 | Diffuse morbilliform maculopapular rash | 20 years old man | Fever and rash simultaneously | Not reported | Trunk, extremities | Not reported | Not reported |
Magro, C. | Complement associated microvascular injury and thrombosis in the pathogenesis of severe COVID‐19 infection: a report of five cases 20 | Retiform purpura with extensive surrounding inflammation | 32 years old male | One week after fever and cough he became ventilator dependent, 4 days after ventilator support skin rash appeared | hydroxychloroquine, azithromycin and remdesivir | Buttocks | There was a significant degree of interstitial and perivascular neutrophilia with prominent leukocytoclasia. IHC showed striking and extensive deposition of C5b‐9 within the microvasculature | Not reported |
Dusky purpuric patches | 66 years old woman | 9 days after having fever, cough, diarrhea and chest pain, she became hypoxemic and after 11 days in hospital skin rash appeared | Hydroxychloroquine, enoxaparin | Palms and soles bilaterally | Extensive vascular deposits of C5b‐9 (figure 6C), C3d, and C4d were observed throughout the dermis, with marked deposition in an occluded artery. | Not reported | ||
Mildly purpuric reticulated eruptions, consistent with livedo racemosa | 40‐year‐old woman | after 2 weeks of dry cough, fever, myalgias, diarrhea, and progressive dyspnea | Not reported | chest, legs and arms | . Significant vascular deposits of C5b‐9 and C4d | Not reported | ||
Chen, Y. | Infants Born to Mothers with a New Coronavirus (COVID‐19) 21 | Diffuse maculopapular rash and Facial skin ulceration | Above 37‐week gestational age infant | edema of the lateral thigh | Nothing | Diffuse | Not reported | 1 day |
First on forehead and progress to diffuse small miliary red papules | Above 37‐week gestational age infant | TTN (transient tachypnea of the newborn) | Nothing | Not reported | Not reported | 8‐9 days | ||
Najarian | Morbilliform exanthem associated with COVID‐19 22 | Pruritic progressive erythematous macules gradually changed to patches | 58‐year‐old Hispanic male | Cough and pain in hands and legs 3 days ago | azithromycin and benzonatate | legs, thighs, forearms, arms, shoulders, back, chest, and abdomen | Not reported | 2 days |
Hoenig, Leonard J. | Rash as a Clinical Manifestation of COVID‐19 Photographs of a Patient 23 | Erythematous, edematous, malar eruption | 26 years old man | Sore throat, malaise, ache, nonproductive cough, anosmia, ageusia, fever | adalimumab | Face | Not reported | 6 days |
Jimenez‐Cauhe, Juan | Reply to “COVID‐19 can present with a rash and be mistaken for Dengue”: Petechial rash in a patient with COVID‐19 infection 24 | Erythemato‐purpuric, millimetric, coalescing macules | 84‐year‐old woman | 3 days after hospitalization (11 days after COVID‐19 symptoms) | hydroxychloroquine and lopinavir/ritonavir | Flexural regions mainly in peri‐axillary area | Not reported | Not reported |
Quintana‐Castanedo, Lucía | Urticarial exanthem as early diagnostic clue for COVID‐19 infection 25 | Pruritic urticarial rash consisting of confluent, edematous and erythematous papules | 61‐year‐old Spanish Medical Doctor | Not reported | No drug during the last 2 months | Thighs, arms, and forearms | Not reported | 7 days |
Miriam Morey | Cutaneous manifestations in the current pandemic of coronavirus infection disease (COVID 2019) 26 | Erythematous, confluent, nonpruritic maculopapular rash | 6‐year old boy | 2 weak after symptoms and 48 hours after confirmed COVID‐19 test | Not reported | Trunk and neck that gradually spread to the cheeks and upper and lower extremities, reaching the palms of the hands | Not reported | 5 days |
Acute urticaria, apparently pruritic | 2‐ month old girl | 4 days after low fever, at the same time with COVID‐19 cinfirm | Not reported | Face and upper extremities and spread in a few hours to the trunk and lower extremities | Not reported | 5 days |
TABLE 2.
First name | Title | Percentage of skin lesions | Skin lesions characteristic | Accompanied by COVID‐19 symptoms | Location of skin lesions | Accompanied by specific symptoms | Age | Duration of skin lesions, mean (days) |
---|---|---|---|---|---|---|---|---|
S. Recalcati | Cutaneous manifestations in COVID‐19: a first perspective 27 | 15% | Erythematous rash | 40% had used new medicine in 15 previous days, 12% were hospitalization | Trunk | Itching was low or absent and usually lesions healed in few days | Not reported | Not reported |
3% | Widespread urticaria | Not reported | Not reported | |||||
1% | Chickenpox‐like vesicles | Not reported | Not reported | |||||
C. Galván Casas | Classification of the cutaneous manifestations of COVID‐19: a rapid prospective nationwide consensus study in Spain with 375 cases 1 | 19% | Erythema with vesicles or pustules (Pseudo‐chilblain) | 59% after other symptoms | Acral areas | Pain (32%) or itch (30%). | younger patients | 12.7 days |
9% | Other vesicular eruptions | 15% before other symptoms | Trunk and limbs | Itching (68%) | middle aged patients | 10.4 days | ||
19% | Urticarial lesions | Not reported | trunk or disperse and palmar | Itching (92%) | Not reported | 6.8 days | ||
47% | Maculopapular eruptions | Not reported | dorsum of the hands | Itching (57% | Not reported | 8.6 days | ||
6% | Livedo or necrosis | Not reported | truncal or acral ischemia | Not reported | older patients | Not reported | ||
Fernandez‐Nieto, D. | Characterization of acute acro‐ischemic lesions in non‐hospitalized patients: a case series of 132 patients during the COVID‐19 outbreak 28 | 72.0% | Chilblain‐like | 12% after other symptoms and 2% at the same time with other symptoms | Acral area (34% hands and 76% feet and 12.6%heels or wrists) | Not reported | Mean of age were 23.4 years old | 9.2 days |
28.0% | Erythema multiformelike | Acral area (21% hands and 94% feet and 27% heels or wrists) | Not reported | Mean of age were 12.2 years old | 7.4 | |||
Gianotti, Raffaele | Clinical and Histopathological study of skin dermatoses in patients affected by COVID‐19 infection in the Northern part of Italy 29 | Not reported | Diffuse maculo‐papulo‐vesicular rash | Lung biopsy of COVID + pneumonia indicates a severe damage of the alveolar epithelial cell floating in the alveolar space just like in bullous severe erythema multiforme in which ballooning keratinocytes detach from the spinous layer. | Arm | classic dyskeratotic cells, ballooning multinucleated cells and sparse necrotic keratinocytes with lymphocytic satellitosis, perivascular spongiotic dermatitis with exocytosis along with a large nest of Langerhans cells and a dense perivascular lymphocytic infiltration eosinophilic rich around the swollen blood vessels with extravasated erythrocytes | Not reported | Not reported |
Not reported | Hemorragic dot‐like area are due to extravasated erytrhocytes | trunk | Not reported | Not reported | ||||
Not reported | Papular erythematous exanthema | trunk | Not reported | Not reported | ||||
Not reported | Diffuse macular livedoid hemorrhagic lesions | leg | Not reported | Not reported | ||||
Piccolo, V. | Chilblain‐like lesions during COVID‐19 epidemic: a preliminary study on 63 patients 30 | 100% | 31/54 erythematous oedematous lesion, 23/54 blister | Gastrointestinal symptoms 11.1%, respiratory symptoms 7.9%, fever 4.8% | Feet (85.7%), hand (6%), hand and feet together (7%) | Pain & itching sensation 27%, both together 20.6% | Median 14 | Not reported |
Hedou, M. | Comment on “Cutaneous manifestations in COVID‐19: a first perspective “by Recalcati S 31 | 4.9% | Erythematous rash, urticaria | Not reported | Face, upper body | Itching | Mean age 47 | Not reported |
Marzano, Angelo Valerio | Varicella‐like exanthem as a specific COVID‐19‐associated skin manifestation: multicenter case series of 22 patients 32 | 100% | Diffuse (scatter) papulovesicular lesions | Fever (95.45%), cough (72.72%), dyspnea (36.36%), headache (50%), coryza (45.45%), weakness (50%), hypogeusia & hyposmia (18.18%), asthenia & myalgia & diarrhea & nausea (4.54%) | Trunk, limbs |
itching (36.36) burning (13%) pain (9%) |
Mean age 56.45 | 7.45 |
Recalcati, S. | Acral cutaneous lesions in the Time of COVID‐19 33 | 100% | Acral red‐purple maculopapular eruption, with possible bolous evoloution or swelling,targetoid lesion | In 3 cases cough and fever 3 weeks before skin manifestation was observed | 8 cases feet,4 hand and 2 cases both area among 14 cases | Mild itching in 3 cases | 11 patients with average 14.4 and 3 with average 29 | 2 to 4 weeks |
TABLE 3.
First author | Title | Skin injuries among medical staff fighting COVID‐19 & general papulation | Percentage | Recommendations |
---|---|---|---|---|
Bahareh Abtahi‐Naeini | Frequent handwashing amidst the COVID‐19 outbreak: prevention of hand irritant contact dermatitis and other considerations 34 | Eczema | Not reported |
|
irritant | Not reported | |||
contact dermatitis | Not reported | |||
methicillin‐resistant Staphylococcus aureus colonization | Not reported | |||
Pingping Lin | Adverse skin reactions among health care workers during the coronavirus disease 2019 Outbreak: A survey in Wuhan and Its surrounding regions 35 | occupational contact dermatitis | 31.5% |
|
dryness or scales | 68.6% | |||
papules or erythema | 60.4% | |||
maceration | 52.9% | |||
Patruno, Cataldo | The role of occupational dermatology in the COVID‐19 outbreak 36 | dryness, irritation, itching, and even fissuring and bleeding | Not reported |
|
hand dermatitis | Not reported | |||
maceration | Not reported | |||
Pei, S. | Occupational skin conditions on the frontline: A survey among 484 Chinese health care professionals caring for COVID‐19 patients 37 | various degrees of pruritus | 61.8% | Not reported |
Mild pruritus | 45.5% | |||
Moderate pruritus | 15.1% | |||
Severe pruritus | 1.2% | |||
various skin lesions | 73.1% | |||
erythema | 38.8% | |||
prurigo | 22.9% | |||
blisters | 13.8% | |||
rahagades | 13.6% | |||
papule/edema | 12.8% | |||
exudation/crust | 6.8% | |||
lichenification | 5.6% | |||
Scratch | 11.7% | |||
Bin Zhang | COVID‐19 epidemic: Skin protection for health care workers must not be ignored 38 | indentations, ecchymosis, maceration, abrasion and erosion | Not reported |
|
blisters and itching and bleeding | Not reported | |||
dermatitis and folliculitis. | Not reported | |||
fungal infections | Not reported | |||
desquamation, rhagades | Not reported | |||
eczema‐like changes | Not reported | |||
ulcers followed by secondary bacterial or fungal infections | Not reported | |||
Qixia Jiang | The Prevalence, Characteristics, and Prevention Status of Skin Injury Caused by Personal Protective Equipment Among Medical Staff in Fighting COVID‐19: A Multicenter, Cross‐Sectional Study 39 | Various type of Skin injury | 42.8% |
|
related pressure injuries | 30% | |||
moist‐associated skin damage (redness, pain, itching, or prickling) | 1.8% | |||
skin tear | 2% | |||
related pressure injuries and moist‐associated skin damage | 78.8% | |||
related pressure injuries and moist‐associated skin damage and skin tear | 13.2% | |||
related pressure injuries and skin tear | 7.0% | |||
moist‐associated skin damage and skin tear | 1.0% | |||
Yan, Y. |
Consensus of Chinese experts on protection of skin and mucous membrane barrier for health care workers fighting against coronavirus disease 2019 40 |
Erythema, dryness, scale, papules, maceration, erosion, contact dermatitis | Not reported |
|
Dirk M. Elston, MD | Occupational skin disease among health care workers during the Coronavirus (COVID‐19) epidemic 5 | Dermatitis | 97.0% |
|
Teresa Oranges | Reply to: “Skin damage among health care workers managing coronavirus disease‐2019” 41 | Hand eczema, skin damage | more than 60% |
|
Jiajia Lan | Skin damage among health care workers managing coronavirus disease‐2019 42 | dryness/tightness and desquamation | 97.0% | Not reported |
Singh, M | Overzealous hand hygiene during COVID‐19 pandemic causing increased incidence of hand eczema among general population 43 | Hand eczema, erythema, scaling and vesiculation | Not reported |
|
TABLE 4.
First author | Title | Location skin injuries among medical staff fighting COVID‐19 | Percentage |
---|---|---|---|
Pingping Lin | Adverse skin reactions among health care workers during the coronavirus disease 2019 outbreak: A survey in Wuhan and its surrounding regions 35 | Hands | 84.6% |
Cheeks | 75.4% | ||
Nasal bridge | 71.8% | ||
Pei, S. | Occupational skin conditions on the frontline: A survey among 484 Chinese health care professionals caring for COVID‐19 patients 37 | Face | 47.1% |
Hands | 27.5% | ||
Limbs | 15.7% | ||
Truncus | 12.6% | ||
Whole body | 2.3% | ||
Bin Zhang | COVID‐19 epidemic: Skin protection for health care workers must not be ignored 38 | Nasal bridge | 83.1% |
Qixia Jiang | The Prevalence, Characteristics, and Prevention Status of Skin Injury Caused by Personal Protective Equipment Among Medical Staff in Fighting COVID‐19: A Multicenter, Cross‐Sectional Study 39 | Nose Bridge | 30.1% |
Cheeks | 28.3% | ||
Ear | 25.3% | ||
Forehead | 14.8% | ||
Jiajia Lan | Skin damage among health care workers managing coronavirus disease‐2019 42 | Nasal bridge | 83.1% |
TABLE 5.
First author | Title | Patient characteristics | Recommendation | The reason | Dose adjustment |
---|---|---|---|---|---|
Rademaker, M. |
Advice regarding COVID‐19 and use of immunomodulators, in patients with severe dermatological diseases 46 |
Patient With inflammatory skin disorder being actively managed with an immunomodulator who confirmed COVID‐19 Disease | should stop the immunomodulator (s) immediately, exception of systemic corticosteroids | COVID‐19 infection being aggravated by immunomodulators and secondary bacterial infection as part of COVID‐19 complication become aggravated too | Not reported |
patient with inflammatory skin disorder being actively managed with an immunomodulator who with signs of common cold but is not formally diagnosed with COVID‐19 disease |
Lowering the dose of immunomodulatory/ or temporarily stopping for 2 weeks. Exception is systemic corticosteroids. |
|
|||
Federico Bardazzi |
Biologic therapy for psoriasis during the COVID‐19 outbreak is not a choice 47 | patient is stable or in good health | It is not reasonable/indicated to suspend the ongoing immunosuppressive/immunomodulatory therapy | as the risk of reactivation of the underlying pathology could add an additional risk factor to infections, including COVID‐19./inhibition of IL‐17 pathway may have beneficial effects in treating COVID‐19 | Not reported |
Shanshal, M. |
Biological treatment uses amid the COVID‐19 era, a close look at the unresolved perplexity 48 |
patients who are already on biological treatment and have tested positive for COVID‐19 | Discontinuing or postponing the biological therapy until full recovery from the COVID‐19 infection. |
patients with existing comorbidities will need extra precaution along with frequent clinical observation and monitoring, some patients with active infection show no symptoms or radiologic abnormalities in the initial presentation and might not realize that they have been infected |
Not reported |
composed of patients who are being considered for the initiation of biological therapy | avoidance of initiation of biologic therapy for high‐risk patients | Not reported | |||
patients with severe psoriasis, those on potentially immunosuppressive therapies, and those presenting comorbid conditions might be at higher risk of infection. | all individuals stop biological treatment as soon as they are diagnosed with COVID‐19 infection | Not reported | |||
Di Lernia, Vito | Biologics for psoriasis during COVID‐19 outbreak 49 | patients on biologics and on immunosuppressants for psoriasis, hidradenitis, atopic dermatitis, pemphigoid, pemphigus, and other conditions | all patients taking biologics wear such coverings or masks when outside the home and practice social distancing | it is neither practical nor logical to cease these over a few weeks while this pandemic is upon us | Not reported |
Megna, M. |
Biologics for psoriasis patients in the COVID‐19 era: more evidence, less fears 50 |
psoriasis patients during COVID‐19 pandemic era |
We strongly believe that proactive biologic discontinuation should be avoided. |
interruption of biologic therapy in psoriatic patients involves a dysregulation of inflammatory cytokines that not only exacerbates psoriasis but is also likely to contribute to a more aggressive organic response to SARS‐CoV‐2, biologics for psoriasis do not increase the risk of viral infections or their complications | Not reported |
Abdelmaksoud, A. |
Comment on “COVID‐19 and psoriasis: Is it time to limit treatment with immunosuppressants? A call for action” 51 |
Older patients with moderate‐to‐severe psoriatic | Not stop systemic biologic or nonbiologic therapy and phototherapy/ interleukin 17 inhibitors should considered in the priority because have lower effects on personal immune functions | users of apremilast, etanercept, and ustekinumab are at lower risk rate of serious infection compared with those on methotrexate, | Not reported |
Conforti, C. |
COVID‐19 and psoriasis: Is it time to limit treatment with immunosuppressants? A call for action 52 |
patient with psoriasis taking immunosuppressive drugs | limit and/or reduce the time of administration, preferring topical and/or drugs with a lower impact on the immune system | these drugs may cause decreased immune response and greater susceptibility to life‐threatening infections | Not reported |
patient with psoriasis taking immunosuppressive drugs who confirmed COVID‐19 | stop all immunosuppressive and biological therapy | Not reported | |||
Price, K. N. | COVID‐19 and immunomodulator/immunosuppressant use in dermatology 53 | Psoriasis Patients treat with Corticosteroids, Tacrolimus, Cyclosporine, Mycophenolate mofetil, Azathioprine, Methotrexate | Consider stopping when viral symptoms present especially with known or potential exposure | Broad immunosuppression across multiple cytokine axes with immunosuppressants has the potential to increase susceptibility, persistence, and reactivation of viral infections. Immunosuppressants decrease cytokines that recruit and differentiate immune cells needed to clear the infection. In addition, inflammatory mediators can become hyperactivated, resulting in a “cytokine storm,” which is the primary cause of death in severe disease. |
Not reported |
psoriasis Patients treat with Infliximab, Etanercept, Certolizumab, Adalimumab, Anakinra (IL‐1) | Continue if viral symptoms are mild, consider stopping if viral symptoms worsen or high fever develops | Not reported | |||
psoriasis Patients treat with Dupilumab (IL‐4) | Continue unless severe symptoms present | Not reported | |||
psoriasis Patients treat with Brodalumab (IL‐17), Secukinumab (IL‐17a), Ixekizumab (IL‐17a), Ustekinumab (IL‐12/23), Guselkumab (IL‐23) | Continue if viral symptoms are mild, consider stopping if viral symptoms worsen or high fever develops | Not reported | |||
psoriasis Patients treat with Rituximab | Consider stopping when viral symptoms present especially with known or potential exposure. | Not reported | |||
psoriasis Patients treat with Apremilast | Continue unless severe symptoms present | Not reported | |||
Wang, C. | COVID‐19 and the use of immunomodulatory and biologic agents for severe cutaneous disease: An Australia/New Zealand consensus statement 54 | Patients on immunomodulators, including biologic agents and new small molecular inhibitors for cutaneous disease, with suspected or confirmed COVID‐19 disease | All immunomodulators used for skin diseases should be immediately withheld, exception of systemic corticosteroid therapy, | immunosuppression is thought to increase susceptibility and cause more severe infection and atypical presentations of coronavirus infections in immunocompromised hosts, including prolonged incubation periods, persistent asymptomatic viral shedding, diarrh oea, weight loss and encephalitis as primary manifestations |
|
on immunomodulators, who develop symptoms or signs of an upper respiratory tract infection, but COVID‐19 is not yet confirmed | dose reduction or temporarily cessation for 1–2 weeks |
there is currently insufficient evidence to suggest that COVID ‐19 infection is aggravated by immunomodulators used in skin disease, however all COVID‐19 infections should be considered serious |
|
||
Well patients on immunomodulators | Immunomodulators and biologics should be continued |
Discontinuation of biologic therapy may result in a loss of treatment response when rechallenged and/or development of drug antibodies |
Not reported | ||
Children patients on immunomodulators, | Dose reduction or cessation of immunomodulators and biologics is not necessary | Not reported | Not reported | ||
Organ Transplant/Bone marrow transplant patients | Immunosuppressive treatments (eg, prednisone, ciclosporin, tacrolimus, azathioprine, mycophenolate, etc.) should not be stopped | Not reported | Not reported | ||
Arora, G | The COVID‐19 outbreak and rheumatologic skin diseases 55 | Patients on Disease‐modifying antirheumatic drugs (DMRD)s, biologics or other immunosuppressive medications | Required to consult their rheumatologist and stop these drugs during an infection | Because patients with rheumatic disease are more susceptible to the COVID‐19 virus either because of the rheumatalogic disease itself or the medications used to treat their underlying disease. | Not reported |
Non‐infected patients | Advised to continue their medication during the epidemic | ||||
Kansal, NK | COVID‐19, syphilis, and biologic therapies for psoriasis and psoriatic arthritis: A word of caution 56 | Patients with psoriasis and psoriasis arthritis | Considering the risk to benefit ratio before discontinuing drugs and monitoring the patients who continue to receive the therapy | Because the prognosis of COVID‐19 cannot be predicted in individual cases (particularly in middle aged and older patients, with co‐morbidities like diabetes mellitus or cardiovascular disease etc, if they are being treated with biologics). | Not reported |
Plachouri, KM | The management of biologics in dermatologic patients in the 2019‐nCoV era 57 | Dermatologic patients | Postpone initiation of biologic treatments in this particular period | The lack of sufficient data concerning the interaction of SARS‐CoV‐2 and biologics is also an important factor that should be taken into consideration when examining the option of initiating therapy with the latter. Another logistic parameter that should not be underestimated is the need of frequent careful monitoring under such treatments that includes both regular laboratory examinations as well as routine dermatologic follow‐up visits, which could constitute a problem under the emerging societal circulatory restrictions that are posed in order to control the pandemic transmission | Not reported |
Brownstone, ND | Novel Coronavirus Disease (COVID‐19) and Biologic Therapy in Psoriasis: Infection Risk and Patient Counseling in Uncertain Times 58 | Psoriatic patients with following risk factors:
|
favoring biologic discontinuation or reduction in immunomodulatory regimen, if reduction is needed option include:
|
These recommendations are based on rate of infections in previous clinical trials studies about biologic and immunosuppressive drugs in psoriatic patients | Not reported |
Psoriatic patients with following risk factors:
|
favoring biologic continuation | Not reported | |||
Patients who test positive for COVID‐19 infection | Advising to hold their biologic dose until their infection clears. | This requires untill improvement in respiratory symptoms, and two negative COVID‐19 test performed 24 hours apart. if COVID‐19 retesting is not available, restarting biologic therapy until 30 days after resolution of fever and respiratory symptoms | |||
Villani, A | Patients with advanced basal cell carcinomas in treatment with sonic hedgehog inhibitors during the coronavirus disease 2019 (COVID‐19) period: Management and adherence to treatment 59 | Patients with advanced basal cell carcinoma receiving treatment with the hedgehog pathway inhibitors sonidegib and vismodegib during the COVID‐19 period | Continuing therapy. Dose adjustment to prolong treatment duration, when possible. | Based on their analysis on 37 patients at Italian referral center for skin cancer diagnosis and management | Not reported |
Gisondi, P | Risk of hospitalization and death from COVID‐19 infection in patients with chronic plaque psoriasis receiving a biological treatment and renal transplanted recipients in maintenance immunosuppressive treatment 60 | Patients with chronic plaque psoriasis receiving a biological treatment and renal transplanted recipients in maintenance immunosuppressive treatment | There is no need to discontinue their therapies | There is no early signal of an increased hospitalization or death from COVID‐19. Based on retrospective observational study in verona | Not reported |
ShakShouk, H | Treatment considerations for patients with pemphigus during the COVID‐19 pandemic 61 | Patients with pemphigus and without active infection | postponing rituximab infusions temporarily | Delaying peak patient immunosuppression during peak COVID‐19 incidence to reduce the risk of adverse outcomes. | Not reported |
glucocorticoids and steroid‐sparing immunosuppressive agents, such as azathioprine and mycophenolate mofetil, should be tapered to the lowest effective dose | Their nonspecific immunosuppressive effects increase infection risk, among other complications, in a dose‐dependent manner. | Not reported | |||
Patients with pemphigus and active COVID‐19 infection | postponing rituximab infusions temporarily | Delaying peak patient immunosuppression during peak COVID‐19 incidence to reduce the risk of adverse outcomes. | Not reported | ||
In active COVID‐19 infection, immunosuppressive steroid‐ sparing medications should be discontinued when possible | Their nonspecific immunosuppressive effects increase infection risk, among other complications, in a dose‐dependent manner. | Not reported | |||
Jic ZA |
United States Cutaneous Lymphoma Consortium Recommendations for Treatment of Cutaneous Lymphomas During the COVID‐19 Pandemic 62 |
Low risk patients with cutaneous lymphomas | Low‐risk therapies that can be utilized at home should be continued for all patients. Home‐based NBUVB and heliotherapy can be continued or initiated. | The risks of travel and exposure likely outweigh the benefit of in‐office treatments such as ultraviolet light therapy and total body electron beam radiation therapy. | Not reported |
Intermediate low risk patients with cutaneous lymphomas | Therapies may be continued, but dose adjustments may be advised on an individual basis. Initiation of these therapies may be postponed using low‐risk bridge therapies short term. Increasing or initiation of a retinoid or interferon should be considered in cases that necessitate the removal of other high‐risk therapies. | Not reported | Not reported | ||
Intermediate high risk patients with cutaneous lymphomas | Not reported | ||||
High risk patients with cutaneous lymphomas | May require travel to the clinic or hospital. These should only be utilized in the highest risk patients and the additional risks of therapy‐related travel should be considered. Infusion regimens may be adjusted to increase treatment intervals. Allogeneic stem cell transplant and treatment with CHOP, alemtuzumab, fludarabine are strongly discouraged, Consider alternative lower risk therapies whenever possible. | Allogeneic stem cell transplant and treatment with CHOP, alemtuzumab, fludarabine are strongly discouraged during the pandemic because they often lead to significant cytopenias that are known risk factors for COVID‐19 complications. | Romidepsin and mogamulizumab may be considered on individual basis with extended intervals and lower doses. | ||
Torres, T | Managing Cutaneous Immune‐Mediated Diseases During the COVID‐19 Pandemic 63 | patients with cutaneous immune‐mediated diseases (including psoriasis, atopic dermatitis, and hidradenitis suppurativa) and without active COVID‐19 infection | Continue their treatment even during the COVID‐19 outbreak |
|
Not reported |
Patients with cutaneous immune‐mediated diseases (including psoriasis, atopic dermatitis, and hidradenitis suppurativa) and with active COVID‐19 infection | Withhold immunosuppressive or biologic treatment | Not reported | Not reported | ||
Megna, M | Biologics for psoriasis in COVID‐19 era: what do we know? 64 | Psoriatic patients without COVID‐19 infection | Treatment discontinuation should be avoided | Unnecessary biologic discontinuation would lead to a worsening of psoriasis and psoriatic arthritis in a high percentage of the cases. As a consequence, there may be higher disease burden, destructive impact on quality of life, as well as increased health care costs due to the augmented number of consultations and recovery. Furthermore, the unavoidable subsequent return to biologic therapy could be associated with switching toward higher cost drugs, due to the well‐known lower efficacy of biologics in the same patient after their interruption | Not reported |
Psoriatic patients with COVID‐19 infection | Treatment discontinuation | Not reported | |||
Amerio, P | COVID‐19 and psoriasis: should we fear for patients treated with biologics 65 | Psoriatic patients | The treatment of psoriatic patients with biologicals should not be discontinued during the time of this pandemic | Based on literature review | Not reported |
elderly patients with coexisting morbidities such as hypertension, diabetes and obesity that enhance their chance of developing, if ever infected, a more severe disease; when patients develop flu like or COVID‐19 specific (anosmia, asthenia) symptoms and if are exposed to high risk contact with infected people | Suspend the treatment should be made | Not reported |
4. DISCUSSION
Coronavirus widespread quickly across the world and in the March 2020,WHO announced the pandemic condition 9 . There is necessity to paying more attention to skin and its appendix (hair, nail) and the mucosal manifestation of COVID‐19 also being more aware of them and updates our knowledge according to the latest reports.
These manifestations could be the presenting signs of COVID‐19 which may help for early disease diagnosis. In addition, we had many concerns about patient who are suffering from chronic dermatologic disorders which needed to have repeated follow ups or who are on immunomodulator agents specifically immunosuppressives that are needed to be controlled without any more risk to getting infected with COVID‐19 or getting involved with its consequences.
4.1. Primary skin manifestations of COVID‐19
4.1.1. Virus related
According to the study which has done among 88 positive patients with COVID‐19, in Italy, 20.4% of patient had skin manifestation that the most common manifestation was erythematous rash or patchy exanthematous red rash. Also, there was urticarial eruption that could be localized or widespread, and 1 case of chickenpox‐like blisters. The most involved area was trunk and all of the lesions were pruritic. There was not no any relation between disease severity and skin manifestations. 27
In a study carried out in France between 103 patients, skin manifestations were seen in 5(4.9%), which were red rashes or urticarial rashes, mostly in the face and upper trunk. And there was a case of HSV‐1 in an intubated patient. 31 There were reports of COVID‐19 patients with mottling or livedo‐reticularis (LR) that could be because of disseminated intravascular coagulation (DIC). 16 Transient LR have been also seen in 2 COVID‐19 patients who were not in bad general condition. 16 Petechial skin rash (Dengue‐like) could be considered as a presenting sign of COVID‐19, like acute hemorrhagic edema of infancy. 8 Symmetrical pruritic papules on both heels which were confluent yellowish‐ erythematous in color appeared 13 days after symptoms onset of COVID‐19 in a 28‐year‐old previously healthy woman, that gradually became erythematous hardened pruritic plaques. 8 Acro‐ischemic lesions (pseudo‐chilblain or Pernio‐like lesion) or “COVID toe” which are micro thrombotic presentations of COVID occur in both children and adolescents when they are in good health condition, and the main affected parts were the feet and hands. The color of lesions were red and purple or blue and they could become blistering or having a black crust. 66
In a study of 63 patients who complained about chilblain like lesions in Italy, the range of patient's age was 12 to 16 years old, and the most affected area was the feet (85.7%), then the both hands plus feet in the second place (7%), and next the only hands (6%). Most lesions were erythematous edematous, and in blistering form. Most of the cases were in good general conditions, some of the patients were symptomatic as, gastrointestinal (11.1%), respiratory (7.9%) or febrile (4.8%) before showing skin manifestations. It was not possible to perform confirmatory tests for SARS‐CoV‐2 in all patients, but in those who did (18 cases), 4 of them turned positive. A study stated the hypothesis of chilblain‐like lesions could be occur because of delayed immune reaction to COVID‐19 in genetically prone ones. 30 A similar study with these finding performed in Spain. 12
In a case series of 14patients, 11 children with average age of 14.4 years and 3 adult patients with average age of 29 years were reported, they did not have any systemic symptoms except cough and fever in 3 cases from 3 weeks before skin eruption onset. The morphology of rash was a red‐purple maculopapular eruption on the feet, hand of both sides and in 2 children papular targetoid lesions appeared on the hands and the elbow after few days. The rash diminished without any treatment during 2 to 4 weeks. The tests of 4 of them showed a negative result for COVID‐19. 33 Acral ischemic lesions, 2 healthy young females who complained of bilateral papules on the dorsum of their fingers in a red‐ purple color reported, a 35‐year‐old patient had another complaint about diffuse redness under the nail of her right thumb. They both confirmed for having SARS‐CoV‐2. 11 Digit ischemia may happen due to transient increase in antiphospholipid antibodies in severe illnesses or in viral disorders. 67 Another assumption was that this digit ischemia could be related to immunological mechanism or prothrombotic activation states. 12 Pruritic lesions in severe COVID‐19‐related respiratory failures revealed an inflammatory thrombogenic vasculopathy with trace amount of C5b_9 and C4d depositions. 20 Maculopapular lesions which were fixed erythematous blanching on the trunk and limbs presented 2 days after onset of COVID infection symptoms in a 57 years old woman with not any significant past medical history. 10
In another case who was a 48 years old man with HTN, 3 days after onset of fever, the macules, papules and petechial lesions appeared in a symmetric pattern in buttocks, popliteal fossae, proximal anterior thighs, and the lower abdomen. The petechial lesions were similar to parvovirus B19 infection. 68
In a 6 years old boy after 14 to 16 days' work‐up for fever and elevated liver enzymes, erythematous, nonpruritic maculopapular rashes appeared first in the trunk and neck and then gradually spread to the other areas. The lesions diminished with no specific therapies after 5 days. 26 A 32 years old healthy female, 6 days after symptomatic current corona virus infection presented with generalized progressive maculopapular and petechial lesions in a reddish base that by the time became scaly, more itchy and less erythematous. 69
In the most cases of maculopapular lesions palmoplantar region and the mucosa were spare. A 60‐year old man with a history of flu‐like symptoms and positive COVID‐19 infection experienced sudden disseminated red macular lesions which turned into papules on bilateral flank, groin, back and proximal lower extremities. 15
In a 71‐year old Caucasian woman scattered maculopapular eruption (morbilliform) with cervical lymphadenopathy, fever and cough was seen in addition to hemorrhagic macular exanthem on the legs. 14 Pruritic Papulovesicular lesions was seen in a 72 years old woman who had a history of flu‐like symptoms 4 days before skin rash appearance and the rash was on sub‐mammary folds, hips and trunk. 14 Petechial lesions have been seen in above case and another one in Thailand who misdiagnosed as dengue fever. 68 , 70 Digitate papulosquamous lesions occurred in a hospitalized old man who infected with COVID‐19. The initiate periumbilical scaly patches widespread rapidly toward flank and thigh and the other areas, some of them were only papular. The lesions resembled pityriasis rosea and diminished suddenly in 7 days. 71 A 34 months old child with conjunctivitis and eyelid dermatitis confirmed SARS‐CoV‐2 in China. 13 Acute urticaria and low‐grade fever was noticed in 2 months girl lasted 4 days, and spread in few hours from face and upper extremities toward lowers limbs and trunk. 26 A 27 years old previously healthy women who complained of diffuse arthralgia, odynophagia and pruritic reddish plaque in the acral area and the face proceed by fever, chills and chest pain. 9 urticaria have been seen in a female patient who just had dry cough in the past days and her CT scan confirmed the COVID‐19 infection. 18 Also in a 61 years old Spanish MD male patient, progressive pruritic urticarial lesions manifested which lasted about 10 days without no other symptoms. 25
A 60‐year old woman with a history of flu‐like and gastrointestinal symptoms 9 days ago, presented to dermatology department with complaint of diffuse urticarial plaques on the trunk, head and limbs. 15 About Febrile rash it could be say that in a 39 years old male patient with 39°C fever and rashes which appeared at the same time of the fever onset presented, the lesions morphology were red, annular, stable plaques in neck, chest, abdomen, upper limbs and palms without involvement of face and the mucosa. The rash were edematous and erythematous and non‐pruritic. He had no medication use in recent days and weeks before initiation of rash. 72 Varicella‐like exanthema was found in a 8 years old girl who had only mild cough 6 days before papulovesicular skin rash starts which had a symmetrical and bilateral pattern on the trunk. The test of she and her family confirmed for SARSCoV‐2.The lesions diminished after a week. 73 Morbilliform exanthema presented in a 58 years old man who complained about cough and pain in limbs, the physician prescribed Azithromycin and Benzonatate for him and after a few days, pruritic progressive erythematous macule appeared in upper and lower limbs, neck and shoulders and trunk which had morbilliform pattern and through the time, lesions expanded and confluent as patches more than 10 cm on the trunk. 22
A 20 years old healthy male who complained of 6‐day lasting fever and rash presented to emergency department and admitted in ICU. He had spreading nonpruritic maculopapular morbilliform rash on her trunk and limbs, respecting face, mucosa and the eyes. His COVID‐19 confirmed in day 2. 19 Skin rash in infants of positive COVID‐19 mother, none of infant had positive test result among those who have been tested (3 of 4), 2 of the infant had two different patterned rashes, one of them diffuse red maculopapules and the other had ulceration on the forehead. Their rash diminished without any treatment. 18 Erythematous rash appeared 4 days after fever and asthenia in a 64 years old woman used oral paracetamol, the erythematous rash extended to the both antecubital fossa, axillary area and the trunk. The rash disappeared in 5 days with no specific treatment while continuing paracetamol intake. The patient's COVID‐19 infection confirmed with positive RT‐PCR. 17 Malar eruption, a 26 years old man, a known case of Crohn disease, who had a history of close contact to a COVID‐19 patient, developed sore throat, anosmia, ageusia, mild dry cough, malaise and chest congestion in the past 2 to 3 week, who presented with asymptomatic red and edematous malar eruption on his face with a low grade fever and mildly tender large cervical lymph node. 23
C. Galván Casas summarized prevalence of different skin lesions of COVID‐19 based on a study among 375 patients in Spain: maculopapular lesions 47%, urticarial eruption 19%, acral erythematous lesions with pustule or vesicle (chilblain like lesion) 19%, other vesicular lesions 9%, and livedo reticularis 6%. 1
4.1.2. Virus treatment‐related
There were several drug regimens used for treatment of COVID‐19 patients, some of which could result in cutaneous side effects like presence of a new dermatoses or flare/aggravation of a previous dermatologic disorder. Till to the last update of this systematic review, generalized pustular reaction and exacerbation of psoriasis due to Hydroxychloroquine were the reported cases of cutaneous adverse reaction of COVID‐19 treatment 33 , 74 , 75 (Table S7).
The following is the most common adverse reactions found in the publications irrespective of this pandemic, which could be in mind for better dermatologic disease approaching (Table S8).
Hydroxychloroquine: Despite the inconclusive result over the implication of Anti‐Malarial drugs; it is used widely for treating COVID‐19 patients. In a study by Sharma et al, a total of 21 unique dermatologic reactions were reported in 3578 patients had Hydroxychloroquine cutaneous adverse drug reactions. The most common was drug eruptions as in maculopapular, erythematous, and urticarial dermatosis. Hyperpigmentation came second followed by pruritis, SJS/TEN and AGEP(Acute generalized exanthematous pustulosis). 2 Dermatologists should consider the COVID‐19 cutaneous manifestations such as erythematous rash, petechia, urticaria as differential diagnosis while assessing the possible Hydroxychloroquine drug reactions. 27
Azithromycin: Azithromycin is another drug used in combination with Hydroxychloroquine in COVID‐19 treatment regimens. Skin adverse events of it may include cutaneous severe skin reaction associated fever, generalized red or purple skin rashes, angioedema, blisters, skin peeling, burning sensation in eyes or painful skin. 76
Antiviral drugs: Several antiviral drugs are used for its treatment as well; including Oseltamivir which could result in SJS/TEN, angioedema and idiosyncratic cutaneous drug reactions. Ribavirin also may cause alopecia, acneiform eruptions, maculopapular and eczematous lesions, localized scleroderma, skin dryness and rash. Other anitiviral drugs such as antiretrovirals are also used in some patient including Lopinavir and Ritanavir. Their adverse effects my presented as maculopapular drug eruptions, exfoliative erythroderma, SJS/TEN, severe cutaneous drug reactions, injection site reactions. 44 , 77
4.1.3. Immunomodulators and dermatologic disorders
In overall, non‐infected non‐at risk patients with immune‐medicated dermatologic disorders under usage of immunosuppressive immunomodulator drugs like biologic agents are not needed to be alter regimen or discontinue the therapies during pandemic, even these drugs may control the deteriorating cytokine storms also prevented disease flare‐ups which both were associated with poorer outcomes and more complications in COVID‐19 course, although strict adherence to quarantine and personal‐social preventive hygiene performances are highly recommended especially in these groups of patients. But in patients who are living in highly prevalent disease area, showing flu like or COVID‐19 specific symptoms (anosmia or asthenia) or who are highly suspected to having had any positive exposures, based on the consult with their physician and considering all circumstances, it is better to have changing in their therapeutic regimens as dose reduction, dose interval increase or temporary discontinuation. Patients with an active COVID‐19 infection should hold the biologic or non‐biologic immunosuppressants until the complete recovery (at least 4 weeks).
In patients who were symptomatic but were no definite cases, therapies should stop for at least 2 weeks. Most of skin diseases which were treated with systemic immunomodulators were usually associated with more severe COVID‐19 morbidity. Dermatologic disorders which were associated with metabolic syndrome, older age or vital organ comorbidities in particular respiratory disorders like patients with psoriasis, hidradenitis suppurativa and atopic tendencies may have poorer prognosis if become infected. Patients with more severe skin disorders (eg, severe psoriasis) were in higher risk for developing pneumonias by any cause that is of great importance in this pandemic. In overall these group of patients may benefit more from future SARS‐Cov‐2 vaccination. Since the chronic nature of this pandemic, specialists should decide based on recent evidence with regard to case‐by case variations considering cost‐benefit ratio and also disease psychological burden. 46 , 54 , 63 , 78 , 79
Biologic immunomodulators especially TNF‐a inhibitors, janus kinase (JAK) inhibitors, anti‐IL 6 (Tocilizumab) may capable to control cytokine storms and it was systemic consequences like ARDS and etc in COVID‐19 course and some trials were conducted to evaluate their efficacy in disease management, so patients who are using these drugs do not be needed to disrupt. 80
Here in we discuss about experts' recommendations of management of specific cutaneous diseases during pandemic:
4.1.4. Immunobullous disorders
Virus could act as target mimicry in immunobullous disorders and may trigger or aggravate disease course but it is not recommended to do not treat properly, since poor disease control have its own consequences; even probable more severe and complicated COVID‐19 infection; due to deregulated inflammatory storms. 61 , 81 , 82 , 83
If possible, postpone rituximab infusions temporarily in management of pemphigus, especially in the case of time approximation regarding peak of drug immunosuppression and peak of society COVID‐19 burden.
Consume the lowest effective dose of corticosteroids and non‐biologic immunosuppressants.
Discontinue steroid sparing agents during active COVID‐19 infection although complete cessation of steroids is not usually possible due to probable adrenal crises.
Consider hydroxychloroquine in elderly patients with pemphigus.
In overall, in the case of urgent needs, IVIG could be a proper rapid response adjuvant immunomodulator therapy (immuneenhancing in a positive way or minimal immunesuppressive prosperities) for management of non‐infected pemphigus or pemphigoid patients or in patients with active COVID‐19 infection (it is effective for both conditions).
Mycophenolate mofetil was not associated with outcome worsening in pemphigus patient affected by COVID‐19 (case report).
Bruton Tyrosine Kinase inhibitor, Ofatumumab and Tocilizumab which act more selectively may be an option in the certain infected cases of pemphigus.
4.1.5. Psoriasis
There were not exact data about incidence of COVID‐19 in psoriatic patients who are under treatment. 47 , 48 , 49 , 50 , 52 , 60 , 64 , 65 , 84 , 85 , 86 , 87
Risk of hospitalization or death is were not higher than normal population in psoriasis patients under treatment with immunomodulators by itself, but psoriasis may be associated with comorbidities like metabolic syndrome especially in elderly people that is associated with higher mortality rate of COVID‐19 infection.
Monotherapy with immunosuppressives, targeted therapies and lack of comorbidities predict the lower associated risk of COVID‐19 complications in psoriatic patients.
There were not enough evidence regarding superiority of any biologic therapies for psoriasis in the SARS‐CoV‐2 outbreak.
Known case of COVID‐19 or patients with confirmed risky exposures, should discontinue biologics but non‐infected non at‐risk patients could continue the treatment as previous.
Preventive cessation of biologic or undertreatment of severe cases are not logical strategies, since resultant disease‐flare up and higher pro‐inflammatory state of patients (other than the significant cost, burden and impaired life quality) prone them to poorer outcomes in the case of possible infection occurrence also initiation of a biologic agent after discontinuation of another one usually accompanies by lesser response.
Initiation of a biologic therapy needed to consider all circumstances and if decided to start, psoriatic patients who have other concomitant comorbidities should have more closed and frequent visits also further monitoring.
There were some case reports regarding management of complicated psoriatic cases who were also affected by COVID‐19, like successful treatment with Guselkumab. 86
4.1.6. Atopic dermatitis
4.1.7. Acne
Systemic retinoids were area of some controversies in the pandemic since mucosal fragility and the altered mucosal thickness, resultant from the isotretinoine may be a susceptibility factor for coronavirus infection or even have higher viral load in mucosal surfaces, on the other hand isotretinoine can help to have better olfactory function. So low‐dose isotretinoin with folic acid supplementation in association with proper nasal mucosal care is recommended for indicated acne management. 89
4.1.8. Future perspective of dermatology during pandemic
Of course we will encounter large volume of reported primary and secondary skin manifestations of COVID‐19 (like new skin presentations, related to virus itself or its treatment) also more exact recommendations for controlling dermatologic disorders during pandemic especially with further reported cases of patients with an evident dermatologic morbidity that are affected by new corona virus and the manner of controlling their underlying skin disease and concomitant infection. Also with increase of global knowledge about basic personal and social preventive health care and hygiene, it may be expected lesser prevalence of cutaneous contagious disorders like warts, bacterial and pathogenic fungal infections, scabies, pediculosis, sexually transmitted disease and so forth. Also a tremendous progression in teledermatology could be another significant outcome.
5. CONCLUSION
In this systematic review, we focused on various aspects of dermatologic fields and COVID‐19 infection. These entities classified as primary specific virus‐induced or virus associated drug‐induced dermatoses and the secondary cutaneous involvements due to circumstances during pandemic. We also discussed on expert recommendations about immune‐mediated dermatologic disorders which were under treatment with immunomodulators.
Erythematous rash or patchy exanthematous red rash, Morbilliform exanthema, Maculopapular rash, urticaria and acute urticaria, Acro‐ischemic lesions (Psuedo‐chilblain or Pernio‐like lesion or “COVID toe”), Digital ischemia, Digitate papulosquamous lesions, Chickenpox‐like blisters, Varicella‐like exanthema, Pruritic Papulovesicular, Petechial skin rash, Acute hemorrhagic edema, livedo‐reticularis (LR), Symmetrical pruritic papules, Conjunctivitis and eyelid dermatitis, Skin rash in infants of positive COVID‐19 mother and Malar eruption were the reported terms for primary skin manifestation of COVID‐19 up to now. Generalized pustular reaction and exacerbation of psoriasis due to Hydroxychloroquine were the reported cases of cutaneous adverse reaction of COVID‐19 treatment.
In overall, non‐infected non‐at risk patients with immune‐medicated dermatologic disorders under usage of immunosuppressive immunomodulator drugs like biologic agents are not needed to alter regimen or discontinue the therapies during pandemic, even these drugs may control the deteriorating cytokine storms also prevent disease flare‐ups which both are associated with poorer outcomes and more complications in COVID‐19 course. Patients with an active COVID‐19 infection should hold the biologic or non‐biologic immunosuppressants until the complete recovery (at least 4 weeks). In patients who are symptomatic but are no definite cases, therapies should stop for at least 2 weeks.
Dermatologic disorders which were associated with metabolic syndrome, older age or vital organ comorbidities in particular respiratory disorders like patients with psoriasis, hidradenitis suppurativa and atopic tendencies had poorer prognosis if become infected. Patients with more severe skin disorders (eg, severe psoriasis) were in higher risk for developing pneumonias by any cause that was of great importance in this pandemic. In overall these group of patients may benefit more from future SARS‐Cov‐2 vaccination.
Of course we will encounter large volume of reported primary and secondary skin manifestations of COVID‐19 (like new skin presentations, related to virus itself or its treatment) also more exact recommendations for controlling dermatologic disorders during pandemic especially with increase our knowledge about management of patients with an especial dermatologic disorder who are affected by new corona virus. High adherence to protective health care strategies and social isolation or distance is the mainstay of better controlling the disease during pandemic and the role of teledermatology is really significant in this area.
CONFLICT OF INTEREST
The authors declare no potential conflict of interest.
AUTHOR CONTRIBUTIONS
The authors contribute equally to all stages of this study. The team has reviewed the manuscript and the data, and all contributors were in full agreement. Azadeh Goodarzi wrote the initial draft, Azadeh Goodarzi, Farnoosh Seirafianpour, Sogand Sodagar, Arash Pour Mohammad, Parsa Panahi, and Samaneh Mozafarpoor wrote the final manuscript and, all the authors made extensive contributions to the final draft of this manuscript. Azadeh Goodarzi edited the document.
Supporting information
ACKNOWLEDGMENTS
This study was supported and ethically approved by Tehran University of Medical Sciences, Tehran, Iran. Also, the authors would like to thank Rasoul Akram Hospital Clinical Research Development Center (RCRDC) for its technical and editorial supports.
Seirafianpour F, Sodagar S, Pour Mohammad A, et al. Cutaneous manifestations and considerations in COVID‐19 pandemic: A systematic review. Dermatologic Therapy. 2020;33:e13986. 10.1111/dth.13986
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