Abstract
Recent studies have focused on the comorbid conditions of the COVID‐19. According to the current studies, numerous diseases including lung disease, cardiovascular disease and immunosuppression appear to be at higher risk for severe forms of the COVID‐19. To date, there are no data in the literature on the comorbid dermatologic diseases and COVID‐19. We tried to analyze the previous dermatological comorbidity of 93 patients with COVID‐19 (51 males, 42 females) who presented to the dermatology outpatient clinics for the last 3 years. The most common dermatologic diseases in patients with COVID‐19 who have dermatologic diseases for the last 3 years were superficial fungal infections (24, 25.8%), seborrheic dermatitis (11, 11.8%), actinic keratosis (10, 10.8%), psoriasis (6, 6.5%), and eczema (6, 6.5%), respectively. In addition, the number of COVID‐19 patients who presented to dermatology in the last 3 months was 17 (11 men, 6 women). The median age of these patients was 58 (minimum 18, maximum 80) years, and the most common dermatologic diseases before diagnosed COVID‐19 were superficial fungal infections (5, 25%), psoriasis (4, 20%), and viral skin diseases (3, 15%). The possible similarity between cutaneous and mucosal immunity and immunosuppression suggests that patients with some dermatologic diseases especially superficial fungal infections and psoriasis may be more vulnerable to the COVID‐19.
Keywords: COVID‐19, dermatology, immunosuppression, psoriasis, SARS‐CoV‐2, superficial fungal infections
1. INTRODUCTION
A novel coronavirus, SARS‐CoV‐2, emerged from China causes COVID‐19, which is quickly spread throughout the world. 1 The pandemic has been spreading to Turkey since March 11, 2020. The number of COVID‐19 cases in Turkey is increasing by more than 4000 new cases a day and reached 47 029, on April 10, 2020. 2 Among patients with COVID‐19, some of them presented to the dermatology outpatient clinic before and during the pandemic. Recent studies have focused on the comorbid conditions of the COVID‐19. According to the current studies, numerous diseases including lung disease, cardiovascular disease and immunosuppression appear to be at higher risk for severe forms of the COVID‐19. 3 In this regard, the study from Wuhan, China reported that 140 patients who were admitted to the hospital with COVID‐19, in which 30% had hypertension and 12% had diabetes mellitus as comorbid diseases. 4 To date, there are no data in the literature on the comorbid dermatologic diseases and COVID‐19. We aimed to investigate the possible relationship between comorbid dermatological diseases and COVID‐19.
2. MATERIALS AND METHODS
This study was carried out retrospectively by analyzing previous dermatological comorbidity of 93 patients with COVID‐19 who have presented to dermatology outpatient clinic, Uşak Training and Research Hospital, in Turkey for the last 3 years.
Patients were divided into three groups: patients who presented to the dermatology outpatient clinic in the last 3 months, 1 year, and 3 years before diagnosed with COVID‐19. The most common dermatologic diseases of these groups were examined.
The data were analyzed using SPSS 20.0 (SPSS Inc., Chicago, Illinois) program. Descriptive statistics are given by giving frequency and percentages. While numerical changes are shown as mean ± SD in a normal distribution, the median value is used in cases without normal distribution.
3. RESULTS
A total of 93 COVID‐19 patients were included in this study, with 51 males and 42 females. The mean age of the patients was 55.28 ± 19.32 years (Table 1). The number of patients in intensive care was six and four of them became exitus.
TABLE 1.
Diagnosis | Age | ||
---|---|---|---|
Minimum | Maximum | Median | |
Superficial fungal infections | 27 | 83 | 66 |
Seborrheic dermatitis | 17 | 75 | 47 |
Actinic keratosis | 60 | 90 | 75.5 |
Psoriasis | 31 | 71 | 58.5 |
Herpes simplex | 18 | 81 | 54 |
Eczema | 35 | 87 | 54 |
The most common dermatologic diseases in patients with COVID‐19 who have dermatologic diseases for the last 3 years were superficial fungal infections (24, 25.8%), seborrheic dermatitis (11, 11.8%), actinic keratosis (10, 10.8%), psoriasis (6, 6.5%), and eczema (6, 6.5%), respectively.
A total of 52 patients with COVID‐19 were seen for dermatologic diseases in the last year. The most common dermatologic diseases were superficial fungal infections (11, 21.2%), seborrheic dermatitis (7, 13.5%), actinic keratosis (6, 11.5%), psoriasis (5, 9.6%), herpes simplex (3, 5.8%), and eczema (3, 5.8%), respectively.
The number of COVID‐19 patients who presented to dermatology outpatient clinic for the last 3 months was 17 (11 men, 6 women). The median age of these patients was 58 (minimum 18, maximum 80) years. The most common diseases were superficial fungal infections (5, 25%), psoriasis (4, 20%), and viral skin diseases (3, 15%). The clinical and demographic characteristics of the COVID‐19 patients who presented to the dermatology clinic for the last 3 months are summarized in Table 2.
TABLE 2.
Number | Age | Gender | Diagnosis | Current position |
---|---|---|---|---|
1 a | 35 | M | Contact dermatitis | Discharged |
2 | 79 | W | Actinic keratosis | Exitus |
3 | 30 | M | Anogenital warts | Discharged |
4 | 18 | M | Herpes simplex | Discharged |
5 | 28 | M | İchthyosis vulgaris | Discharged |
6 | 58 | M | Contact dermatitis | Exitus |
7 | 70 | M | Xerosis cutis | Discharged |
8 | 59 | M | Molluscum contagiosum | Discharged |
9 b | 47 | W | Psoriasis | Admitted |
10 b | 58 | M | Psoriasis/tinea cruris | Discharged |
11 | 60 | W | Psoriasis/tinea corporis | Discharged |
12 | 71 | M | Psoriasis | Discharged |
13 | 68 | W | Seborrheic dermatitis/actinic keratosis | Discharged |
14 | 40 | W | Cellulitis | Discharged |
15 | 62 | M | Tinea unguinum | Admitted |
16 | 80 | W | Tinea cruris | Exitus |
17 | 27 | M | Tinea unguinum | Discharged |
Abbreviations: M, man; W, woman.
The patient received intramuscular steroid 1 month before diagnosed with COVID‐19.
Patients had been receiving methotrexate.
4. DISCUSSION
This is the first report and perspective of concomitant dermatologic diseases before diagnosed COVID‐19. According to our study, superficial fungal infections, psoriasis, seborrheic dermatitis, actinic keratosis, and herpes simplex are the most common dermatologic diseases before COVID‐19 infection. Older adults who have at greater risk for COVID‐19 can be as a possible predisposing factor for some of the current dermatologic diseases such as actinic keratosis. 5 In our study, psoriasis was among more common dermatological diseases in patients with COVID‐19, especially for the last 3 months. The stress burden caused by the COVID‐19 pandemic in patients with psoriasis might lead to an increase the number of visits of these patients to dermatology outpatient clinics in the last 3 months. 6 The use of immunosuppressive drugs may also have been related to the greater number of psoriasis which is present in patients with COVID‐19. In this context, two of our patients were under methotrexate treatment when infected with a novel coronavirus. While one of these two patients was discharged, the other continues to be hospitalized without intensive care. Furthermore, it can be speculated that the long‐term widespread use of potent topical corticosteroids may also contribute to increased vulnerability to the COVID‐19, given other COVID‐19 patients with psoriasis and eczema. These findings indicate that not only biological agents but also topical and conventional immunosuppressive treatments may cause the predisposition to COVID‐19 during the pandemic. 7 , 8 In this regard, one of the treatment strategies of moderate‐to‐severe psoriasis may be to extend the immunosuppressive treatment during a COVID‐19 pandemic.
The similarity between cutaneous and mucosal immunity suggests that decreased cutaneous immunity may indicate decreased mucosal immunity. 9 , 10 SARS‐CoV‐2 makes infection via pass through nasal mucosa by using angiotensin‐converting enzyme 2 receptor which is found in the basal layer of the nonkeratinizing squamous epithelium. 11 The previous studies revealed that the power of the mucosal innate and adaptive immune systems which contains CD4+ T‐helper cells, Th17, high‐avidity CD8+ CTL, and secretory IgA and IgG1 neutralizing antibodies may prevent viral spreading into the nasal mucosa. These suggestions allow knowing the importance of mucosal immunity on the SARS‐CoV‐2. 12 , 13 Of note, the previous animal study reported that Th1 and Th17 immune responses including IL‐17A and IFN‐γ, which are also important factors to prevent viral damage in the nasal mucosa, are individually unnecessary but together contribute to the optimal healing of superficial fungal infections. 14 Therefore, it can be concluded that patients with a superficial fungal infection may have decreased cutaneous immunity as well as mucosal immunity. This may be one of the explanations of why a patient with superficial fungal infections may indicate to be more prone to COVID‐19 infections. The determination of the relationship between cutaneous and mucosal immunity may lead to developing a preventive treatment approach strategy in patients with immune‐related skin diseases in COVID‐19 and possibly other viral pandemics. 15 The herpes simplex, which is another common disease in patients, with COVID‐19 can also be considered in this regard. Therefore, zinc that is used to prevent recurrent herpes simplex by stimulating the presence of antiviral interferon IFN‐α and IFN‐γ may reduce the contamination of COVID‐19. 16 , 17 Further studies should be conducted to illuminate the appropriate approach to the COVID‐19. Lastly, according to our study, seborrheic dermatitis was another common skin disease among patients with COVID‐19. The possible etiological factors of seborrheic dermatitis such as an increased number of Malassezia species and decreased serum zinc levels in these patients may also play an important role in the contamination of COVID‐19. 18 , 19
The possible similarity between cutaneous and mucosal immunity and immunosuppression suggests that patients with certain dermatologic diseases especially superficial fungal infections and psoriasis may be more vulnerable to the COVID‐19. Randomized controlled trials and large population studies should be conducted to evaluate these findings.
Kutlu Ö, Metin A. Dermatological diseases presented before COVID‐19: Are patients with psoriasis and superficial fungal infections more vulnerable to the COVID‐19? Dermatologic Therapy. 2020;33:e13509. 10.1111/dth.13509
REFERENCES
- 1. Guo YR, Cao Q‐D, Hong Z‐S, et al. The origin, transmission and clinical therapies on coronavirus disease 2019 (COVID‐19) outbreak–an update on the status. Mil Med Res. 2020;7(1):1‐10. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2. https://covid19.saglik.gov.tr/
- 3. Fang L, Karakiulakis G, Roth M. Are patients with hypertension and diabetes mellitus at increased risk for COVID‐19 infection? Lancet Respir Med. 2020;8(4):e21. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4. Zhang JJ, Dong X, Cao YY, et al. Clinical characteristics of 140 patients infected with SARS‐CoV‐2 in Wuhan. China Allergy. 2020. 10.1111/all.14238. [DOI] [PubMed] [Google Scholar]
- 5. Conforti C, Cannavò SP, Jafferany M, et al. Coronavirus disease 2019 (COVID‐19): facts and controversies. Dermatol Ther. 2020. 10.1111/dth.13366. [DOI] [PubMed] [Google Scholar]
- 6. Kutlu Ö, Metin A. A case of exacerbation of psoriasis after oseltamivir and hydroxychloroquine in a patient with COVID‐19: will cases of psoriasis increase after COVID‐19 pandemic? Dermatol Ther. 2020. 10.1111/dth.13383. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Conforti C, Giuffrida R, Dianzani C, Di Meo N, Zalaudek I. COVID‐19 and psoriasis: is it time to limit treatment with immunosuppressants? A call for action. Dermatol Ther. 2020. 10.1111/dth.13298. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8. Abdelmaksoud A, Goldust M, Vestita M. Comment on “COVID‐19 and psoriasis: is it time to limit treatment with immunosuppressants? A call for action”. Dermatol Ther. 2020. 10.1111/dth.13360. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9. Kutlu Ö, Doğan Z, Ekşioğlu H, Kekilli M. Relationship between helicobacter pylori infection and pityriasis versicolor: can helicobacter pylori infection be a new etiologic factor for pityriasis versicolor? Turk J Med Sci. 2020. 10.3906/sag-1910-48. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10. Hovav AH. Mucosal and skin langerhans cells—nurture calls. Trends Immunol. 2018;39(10):788‐800. [DOI] [PubMed] [Google Scholar]
- 11. Lin L, Lu L, Cao W, Li T. Hypothesis for potential pathogenesis of SARS‐CoV‐2 infection a review of immune changes in patients with viral pneumonia. Emerg Microbes Infect. 2020;9(1):727‐732. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12. Prasad A. Local ımmunity concept in the context of the novel corona viral ınfection: a consideration. Asian J Immunol. 2020;3(2):16‐25. [Google Scholar]
- 13. Belyakov IM, Hel Z, Kelsall B, et al. Mucosal AIDS vaccine reduces disease and viral load in gut reservoir and blood after mucosal infection of macaques. Nat Med. 2001;7(12):1320‐1326. [DOI] [PubMed] [Google Scholar]
- 14. Heinen MP, Cambier L, Antoine N, et al. Th1 and Th17 immune responses act complementarily to optimally control superficial dermatophytosis. J Invest Dermatol. 2019;139(3):626‐637. [DOI] [PubMed] [Google Scholar]
- 15. Grant WB, Lahore H, McDonnell SL, et al. Evidence that vitamin d supplementation could reduce risk of ınfluenza and COVID‐19 ınfections and deaths. Nutrients. 2020;12(4):988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16. Cakman I, Kırchener H, Rınk L. Zinc supplementation reconstitutes the production of interferon‐α by leukocytes from elderly persons. J Interferon Cytokine Res. 1997;17(8):469‐472. [DOI] [PubMed] [Google Scholar]
- 17. Razzaque M. COVID‐19 pandemic: can maintaining optimal zinc balance enhance host resistance? Preprints. 2020. 10.20944/preprints202004.0006.v1. [DOI] [PubMed] [Google Scholar]
- 18. Wikramanayake TC, Borda LJ, Miteva M, Paus R. Seborrheic dermatitis‐looking beyond malassezia. Exp Dermatol. 2019;28(9):991‐1001. [DOI] [PubMed] [Google Scholar]
- 19. Aktaş Karabay E, Aksu ÇA. Serum zinc levels in seborrheic dermatitis: a case‐control study. Turk J Med Sci. 2019;49(5):1503‐1508. [DOI] [PMC free article] [PubMed] [Google Scholar]