Hydrochlorothiazide and increased risk of atypical fibroxanthoma and pleomorphic dermal sarcoma

Author:

Kuntz Thomas12,Grimm Alexander2,Hofmann Silke C.3ORCID,Michalowitz Alena‐Lioba2,Schaller Jörg4,Hellmich Martin5,Assaf Chalid6,Oellig Frank7,Kreuter Alexander24ORCID

Affiliation:

1. Department of Dermatology and Venereology University of Cologne Cologne Germany

2. Department of Dermatology Venereology and Allergology Helios St. Elisabeth Hospital Oberhausen University of Witten‐Herdecke Oberhausen Germany

3. Department of Dermatology Allergology und Dermatosurgery Helios University Hospital Wuppertal University of Witten‐Herdecke Wuppertal Germany

4. Department of Dermatology Venereology and Allergology Helios St. Johannes Hospital Duisburg Duisburg Germany

5. Institute of Medical Statistics and Computational Biology Faculty of Medicine and University Hospital Cologne University of Cologne Cologne Germany

6. Department of Dermatology and Venereology Helios Klinikum Krefeld Krefeld Germany

7. Institute of Pathology Mülheim an der Ruhr, Germany

Abstract

SummaryBackground and ObjectivesPrevious work has demonstrated that hydrochlorothiazide (HCTZ) is a risk factor for squamous cell carcinomas (SCC) and basal cell carcinomas (BCC) due to pro‐photocarcinogenic effects. Atypical fibroxanthoma (AFX) and pleomorphic sarcoma (PDS), both ultraviolet‐induced cancers, display a rare but rising cutaneous tumor entity. This study aimed to evaluate if the use of HCTZ is higher in patients with AFX/PDS than in patients with SCC/BCC and subsequently may be a risk factor for AFX/PDS‐development.Patients and MethodsIn a retrospective study of four German skin cancer centers, AFX/PDS cases and SCC/BCC controls were sex and age matched (1:3) over a time‐period of 7 years (2013–2019) to evaluate the use of HCTZ, immunosuppressive medication, second malignancies, and presence of diabetes mellitus.ResultsOverall, 146 AFX/PDS and 438 controls (SCC/BCC) were included in the study. The use of HCTZ was significantly higher in patients with AFX/PDS (44.5%) compared to patients with SCC/BCC (25.3%). Additionally, the presence of diabetes mellitus was significantly higher in AFX/PDS patients.ConclusionsThis study demonstrates a significantly higher use of HCTZ in patients with AFX/PDS compared to SCC/BCC. This result suggests that HCTZ may be a risk factor for AFX/PDS. Additionally, diabetes mellitus or its comorbidities may be associated with an increased risk for AFX/PDS.

Publisher

Wiley

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