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Funding sources
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Editor,
Primary cutaneous lymphomas (PCLs) are rare non‐Hodgkin’s lymphomas that are present in the skin without any extracutaneous involvement at the time of initial diagnosis. 1 The group of PCLs shows distinct clinical, histological, immunophenotypic and genetic characteristics. 2
Coronavirus Disease 2019 (COVID‐19) is the disease caused by SARS‐CoV‐2 infection. It has been accelerating since the beginning of 2020 and is still challenging the healthcare systems worldwide.
Studies suggest that patients with older age and malignancy have a higher risk of severe events including death due to COVID‐19. 3 , 4 Patients with primary cutaneous lymphoma receive immunosuppressive therapy long term for disease control, have potential underlying predisposing conditions (e.g. hypertension and diabetes) and tend to be older.
There are no enough data in the literature about COVID‐19 infection and cutaneous lymphomas.
The aims of our study were to evaluate the incidence of COVID‐19 and severe outcomes of patients with PCL, and describe changes in lymphoma staging after COVID‐19.
We performed a prospective study of patients with PCL at the Dermatology venerology Department, Military Hospital Instruction Mohammed V between June 2020 and June 2021.
We collected all patients with COVID‐19 and described their clinical data and evolution. All statistical calculations were performed using Jamovi ver. 2.2.2.
COVID‐19 outcomes included mild, moderate and severe. This classification was established based on clinical, biological and radiographic evidence:
Mild Illness: Individuals who have any of the various signs and symptoms of COVID‐19 but who do not have shortness of breath, dyspnoea or abnormal chest imaging.
Moderate Illness: Individuals who show evidence of lower respiratory disease during clinical assessment or imaging and who have an oxygen saturation (SpO2) ≥ 94%.
Severe Illness: Individuals who have SpO2 < 94% on room air at sea level.
Our study included 48 patients (96% Mycosis fungoides/Sézary (MF/SS), 4% non‐MF/SS primary cutaneous lymphomas); 40% were IA stage, and 21 patients (60%) received systemic treatment.
Nine Patients (18%) did not receive COVID‐19 vaccines, 17 patients (35%) received partial immunization and 22 patients (45%) received complete immunization.
Thirty‐six patients (75%) suffered from COVID‐19, median age of 55.2 years (SD = 15.5); The sex ratio of males to females was 2.9.
The most common clinical manifestations of COVID‐19 were fever (75%), fatigue (52%), headache (50%), anosmia (38%), diarrhoea (30%), dysgeusia (27%) and dyspnoea (19%).
Comorbidities including smoking, diabetes, hypertension, bronchial asthma and ischaemic heart disease were common in the PCL patients COVID‐19 positives.
All baseline clinical characteristics and evolution are listed in Table 1.
Table 1.
Variables | Characteristics |
---|---|
Comorbidity | |
Smoking | 4 (11%) |
Diabetes mellitus | 10 (27%) |
Hypertension | 8 (22%) |
Bronchial asthma | 2 (5%) |
Ischaemic heart disease | 3 (8%) |
Clinical manifestations | |
Diarrhoea | 11 (30%) |
Abdominal pain | 8 (22%) |
Anosmia | 14 (38%) |
Dysgeusia | 10 (27%) |
Fever | 27 (75%) |
Dyspnoea | 7 (19%) |
Headache | 18 (50%) |
Fatigue | 19 (52%) |
Rhinorrhoea | 6 (16%) |
Skin rash | 1 (2%) |
COVID formes | |
Mild | 9 (25%) |
Moderate | 12 (33%) |
Severe | 15 (42%) |
Outcome at end of lock down | |
Improvement | 2 (6%) |
Stationary | 30 (85%) |
Progression | 4 (9%) |
The haematological and coagulation parameters are presented in Table 2. In all, 25% patients experienced mild disease, 33% moderate disease and 42% severe disease: 46% required hospitalization, 26% needed ICU and 20% died.
Table 2.
Laboratory data | Normal range | COVID‐19 Negative (n = 12) | COVID‐19 Positive (n = 36) | P value |
---|---|---|---|---|
Creatinine (mg/L) | 6–13 | 8.83 ± 1.64 | 11.1 ± 2.57 | 0.008* |
CRP (mg/L) | <5 | 5.67 ± 2.10 | 234 ± 62.4 | <0.001* |
ALT (Units/L) | <40 | 36.92 ± 14.24 | 34.1 ± 8.71 | 0.409 |
AST (Units/L) | <35 | 31 ± 9.18 | 29.9 ± 15.3 | 0.858 |
LDH (Units/L) | 125–243 | 174.58 ± 29.17 | 343 ± 78.8 | <0.001* |
hs Troponin‐I (ng/L) | 2–34 | 12.33 ± 8.8 | 29.7 ± 15.9 | <0.001* |
Serum Ferritin (ng/mL) | 23.9–336.2 | 133 (53.3–263) | 554 (467–847) | <0.001* |
Fibrinogen (g/day) | 2–4 | 4.53 ± 2.68 | 5.02 ± 1.57 | 0.561 |
WBC (× 103/µL) | 4–10 | 9.24 ± 6.71 | 9.48 ± 5.53 | 0.918 |
Hb (g/dL) | 13–17 | 11.13 ± 2.47 | 12.27 ± 5.65 | 0.341 |
Platelet (× 103/µL) | 150–450 | 258.90 ± 136.12 | 219.37 ± 111.14 | 0.407 |
Lymphocytes (× 103/µL) | 1.5–4 | 1.78 ± 1.19 | 4.56 ± 17.3 | 0.319 |
P < 0.05.
The proportion of mortality in our patients is 8% vs. 1.7% in our Hospital.
Totally 85% of patients reported stability of their PCLs, 6% improvement and 9% worsening.
There were limited data regarding PCL and COVID‐19.
Our study suggests that patients who suffer from PCLs may represent a risk group for potential life‐threatening complications in case of infection with SARS‐CoV‐2.
Risk factors for infections in PCL patients include lymphopenia, chronic organ failure (renal, cardiac or respiratory), Sezary syndrome, other comorbidities (e.g. diabetes and hypertension), aggressive immunosuppressive treatment, advanced/aggressive disease and older age leading to severe COVID‐19 symptoms. 5
Several guidelines for the management and the treatment of cutaneous lymphoma during the COVID‐19 pandemic have been recently established by the United States CL Consortium and the EORTC CLTF. 6 , 7
In conclusion, physicians should consider that PCL patients are at risk for severe COVID‐19; therefore, reinforced preventive measures and prioritization in vaccination strategies are required.
Contributor Information
H. Kerrouch, Email: hasnakerrouch@gmail.com.
M. Khalidi, Email: drkhalidimeryem@gmail.com
R. Frikh, Email: rfrikh@gmail.com
N. Hjira, Email: naoufalhjira@gmail.com
M. Boui, Email: m.boui@um5r.ac.ma
Data availability statement
Data openly available in a public repository that issues datasets with DOIs.
References
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Associated Data
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Data Availability Statement
Data openly available in a public repository that issues datasets with DOIs.