Literature DB >> 35278240

Primary cutaneous lymphoma and risk for severe COVID-19: a prospective study of 48 cases in Morocco.

H Kerrouch1, M Khalidi1, R Frikh1, N Hjira1, M Boui1.   

Abstract

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Year:  2022        PMID: 35278240      PMCID: PMC9114926          DOI: 10.1111/jdv.18057

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN: 0926-9959            Impact factor:   9.228


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None. 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. The group of PCLs shows distinct clinical, histological, immunophenotypic and genetic characteristics. 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. , 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

Baseline clinical characteristics and evolution of the PCL patients COVID positive (n = 36)

Variables Characteristics
Comorbidity
Smoking4 (11%)
Diabetes mellitus10 (27%)
Hypertension8 (22%)
Bronchial asthma2 (5%)
Ischaemic heart disease3 (8%)
Clinical manifestations
Diarrhoea11 (30%)
Abdominal pain8 (22%)
Anosmia14 (38%)
Dysgeusia10 (27%)
Fever27 (75%)
Dyspnoea7 (19%)
Headache18 (50%)
Fatigue19 (52%)
Rhinorrhoea6 (16%)
Skin rash1 (2%)
COVID formes
Mild9 (25%)
Moderate12 (33%)
Severe15 (42%)
Outcome at end of lock down
Improvement2 (6%)
Stationary30 (85%)
Progression4 (9%)
Baseline clinical characteristics and evolution of the PCL patients COVID positive (n = 36) 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 of PCL patients COVID‐19 (n = 48)

Laboratory data Normal range COVID‐19 Negative (n = 12) COVID‐19 Positive (n = 36) P value
Creatinine (mg/L) 6–138.83 ± 1.6411.1 ± 2.570.008*
CRP (mg/L) <55.67 ± 2.10234 ± 62.4<0.001*
ALT (Units/L) <4036.92 ± 14.2434.1 ± 8.710.409
AST (Units/L) <3531 ± 9.1829.9 ± 15.30.858
LDH (Units/L) 125–243174.58 ± 29.17343 ± 78.8<0.001*
hs Troponin‐I (ng/L) 2–3412.33 ± 8.829.7 ± 15.9<0.001*
Serum Ferritin (ng/mL) 23.9–336.2133 (53.3–263)554 (467–847)<0.001*
Fibrinogen (g/day) 2–44.53 ± 2.685.02 ± 1.570.561
WBC (× 103/µL) 4–109.24 ± 6.719.48 ± 5.530.918
Hb (g/dL) 13–1711.13 ± 2.4712.27 ± 5.650.341
Platelet (× 103/µL) 150–450258.90 ± 136.12219.37 ± 111.140.407
Lymphocytes (× 103/µL) 1.5–41.78 ± 1.194.56 ± 17.30.319

P < 0.05.

Laboratory data of PCL patients COVID‐19 (n = 48) 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. 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. , 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.
  7 in total

1.  Infectious events and associated risk factors in mycosis fungoides/Sézary syndrome: a retrospective cohort study.

Authors:  R Blaizot; E Ouattara; A Fauconneau; M Beylot-Barry; A Pham-Ledard
Journal:  Br J Dermatol       Date:  2018-10-12       Impact factor: 9.302

Review 2.  Cutaneous lymphomas-An update 2019.

Authors:  Werner Kempf; Anne-Katrin Zimmermann; Christina Mitteldorf
Journal:  Hematol Oncol       Date:  2019-06       Impact factor: 5.271

Review 3.  The 2018 update of the WHO-EORTC classification for primary cutaneous lymphomas.

Authors:  Rein Willemze; Lorenzo Cerroni; Werner Kempf; Emilio Berti; Fabio Facchetti; Steven H Swerdlow; Elaine S Jaffe
Journal:  Blood       Date:  2019-01-11       Impact factor: 22.113

4.  United States Cutaneous Lymphoma Consortium recommendations for treatment of cutaneous lymphomas during the COVID-19 pandemic.

Authors:  John A Zic; Weiyun Ai; Oleg E Akilov; Joi B Carter; Madeleine Duvic; Francine Foss; Michael Girardi; Alejandro A Gru; Ellen Kim; Amy Musiek; Elise A Olsen; Stefan M Schieke; Michi Shinohara; Jasmine M Zain; Larisa J Geskin
Journal:  J Am Acad Dermatol       Date:  2020-04-16       Impact factor: 11.527

5.  Prevalence of comorbidities and its effects in patients infected with SARS-CoV-2: a systematic review and meta-analysis.

Authors:  Jing Yang; Ya Zheng; Xi Gou; Ke Pu; Zhaofeng Chen; Qinghong Guo; Rui Ji; Haojia Wang; Yuping Wang; Yongning Zhou
Journal:  Int J Infect Dis       Date:  2020-03-12       Impact factor: 3.623

6.  Comorbidities and multi-organ injuries in the treatment of COVID-19.

Authors:  Tianbing Wang; Zhe Du; Fengxue Zhu; Zhaolong Cao; Youzhong An; Yan Gao; Baoguo Jiang
Journal:  Lancet       Date:  2020-03-11       Impact factor: 79.321

7.  Management of primary cutaneous lymphoma patients during COVID-19 pandemic: EORTC CLTF guidelines.

Authors:  E Papadavid; J Scarisbrick; P Ortiz Romero; P Guaglino; M Vermeer; R Knobler; R Stadler; M Bagot
Journal:  J Eur Acad Dermatol Venereol       Date:  2020-07-07       Impact factor: 9.228

  7 in total

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