Cutaneous T‐cell lymphoma after chronic exposure to hydrochlorothiazide: pharmacovigilance analysis from the RADAR (Research on Adverse Drug events And Reports) Program

Of the 382 patients diagnosed with COVID-19, 70 (18.3%) exhibited dermatological symptoms, that was similar to the literature. Most common complaints were rash (n = 37), redness (n = 29), bruising (n = 13) and wounds (n = 7; Table 1). The number of patients with more than one dermatological symptom was 13/70. Itching occurred in 58 (15.2%) patients, of which 28 did not show any additional symptoms. Similar symptoms were also seen as reactions related to drug use. Whether the symptoms started before or after the COVID-19 treatment was also examined in the present study. Of the patients, 31 stated that the symptoms started before the treatment and 39 said after the treatment. It was necessary to distinguish whether the complaints, which started after the treatment, were due to infection or drug use. The localization and distribution of lesions during a dermatological examination are very important. Sachdeva et al. described lesion localization on hands and feet on the body (69.4%). Recallti et al. identified the main affected area as the body in 18 patients with dermatological findings. The lesions were observed mostly on lower extremities, upper extremities and head–neck region (n = 32/70, 30/70 and 22/70, respectively) in our study. A study on 507 patients reported that 272 (60.44%) of the patients with dermatological symptoms were women. Similar to this study, more women described dermatological symptoms in our study (62.8%). Personal hygiene has become very important during the pandemic. Frequent washing of the hands is recommended for preventing contamination. In the present study, 6.8% of the patients developed hand eczema and 11.5% an intolerance against the soap. In addition, 23% of the patients reported dryness of the skin after the infection, and 9.4% reported redness and itching due to the use of masks. Parameters, such as fever during the COVID-19 infection, length of hospital stay, intensive care and healing time, give an idea about the severity of the disease. Recallti et al. did not find any correlation between cutaneous findings and the severity of the disease. However, in the present study, fever, hospitalization, need for intensive care and length of hospital stay were found to be significantly higher in patients with dermatological symptoms, suggesting a correlation between the severity of COVID-19 infection and dermatological symptoms (Table 2). Dermatological symptoms occur in approximately one-fifth of patients diagnosed with the COVID-19 infection, regardless of the severity of the disease. It is important to inquire about dermatological symptoms and systemic findings in these patients. Multicenter studies with larger patient populations can help in providing more details in this regard.

[1]  Ü. Gül COVID-19 and dermatology , 2020, Turkish journal of medical sciences.

[2]  Hong Liu,et al.  COVID‐19 and cutaneous manifestations: a systematic review , 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

[3]  C. A. González-Cruz,et al.  Classification of the cutaneous manifestations of COVID‐19: a rapid prospective nationwide consensus study in Spain with 375 cases , 2020, The British journal of dermatology.

[4]  M. Ziv,et al.  Cutaneous manifestations of COVID-19: Report of three cases and a review of literature , 2020, Journal of Dermatological Science.

[5]  F. Carsuzaa,et al.  Comment on ‘Cutaneous manifestations in COVID‐19: a first perspective’ by Recalcati S , 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

[6]  S. Recalcati Cutaneous manifestations in COVID‐19: a first perspective , 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

[7]  Z. Memish,et al.  The continuing 2019-nCoV epidemic threat of novel coronaviruses to global health — The latest 2019 novel coronavirus outbreak in Wuhan, China , 2020, International Journal of Infectious Diseases.

[8]  P. Puddu,et al.  Thiazides and Nonmelanoma Skin Cancer: is it a Class Effect? , 2019, Journal of the American Academy of Dermatology.

[9]  A. Pottegård,et al.  Association of Hydrochlorothiazide Use and Risk of Malignant Melanoma , 2018, JAMA internal medicine.

[10]  A. Pottegård,et al.  Hydrochlorothiazide use and risk of nonmelanoma skin cancer: A nationwide case‐control study from Denmark , 2017, Journal of the American Academy of Dermatology.

[11]  A. Rademaker,et al.  Melanoma and Non-Melanoma Skin Cancer Associated with Angiotensin-Converting-Enzyme Inhibitors, Angiotensin-Receptor Blockers and Thiazides: A Matched Cohort Study , 2017, Drug Safety.

[12]  M. Duvic,et al.  Hydrochlorothiazide and cutaneous T cell lymphoma , 2013, Cancer.

[13]  C. Proby,et al.  Known and potential new risk factors for skin cancer in European populations: a multicentre case–control study , 2012, The British journal of dermatology.

[14]  H. Sørensen,et al.  Use of photosensitising diuretics and risk of skin cancer: a population-based case–control study , 2008, British Journal of Cancer.

[15]  A. Mitchell,et al.  Recent patterns of medication use in the ambulatory adult population of the United States: the Slone survey. , 2002, JAMA.