Bernat Mas Matas
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Bernat Mas Matas has a total of 27 co-authors. Here are the top co-authors by number of shared publications:
- Adrián Imbernón-Moya
Servicio de Dermatología, Hospital Universitario Severo Ochoa, Leganés, Madrid, Spain
1 shared publication - Amador Solá-Truyols
Servicio de Dermatología, Hospital Universitario Son Llàtzer, Palma de Mallorca, Spain
1 shared publication - Andrea Ciudad
Servicio de Dermatología, Hospital del Mar, Instituto Hospital del Mar de Investigaciones Médicas (IMIM), Departament de Medicina i Ciències de la Vida (MELIS), Universitat Pompeu Fabra, Barcelona, Spain
1 shared publication - David Pesqué
Department of Dermatology Hospital del Mar Research Institute Barcelona Spain
1 shared publication - Diego de la Vega Ruiz
Servicio de Dermatología, Hospital Universitario Fundación Alcorcón, Madrid, Spain
1 shared publication - Emili Masferrer
Servicio de Dermatología, Hospital Universitario de Terrassa, Terrassa, Barcelona, Spain; Universitat Central de Catalunya, Vic, Spain
1 shared publication
Latest Publications
- Open Access
- 12 March 2026
- Published by Medical Journals Sweden AB in Acta Dermato-Venereologica
- Vol. 106
Cutaneous Leishmaniasis in Patients under Biologic Therapies: A Spanish CLINI-AEDV Multicentre Study
Anti-TNFα agents have been associated with the reactivation of granulomatous infections, including leishmaniasis. Cases of atypical or recurrent cutaneous (CL) or mucocutaneous leishmaniasis (MCL) have been reported in patients on biologics. We conducted a retrospective analysis of a multicenter database to describe the clinical characteristics and management of CL and MCL in patients receiving biological therapy in an endemic area. Clinical features, diagnostics, therapies, and outcomes were analyzed. Seventy-one patients were included (63 CL and 8 MCL). The most common underlying condition was inflammatory bowel disease (33.8%). Lesions were multifocal in 40% and larger than 1 cm in 94.4%. Treatment failures were more frequent in MCL (50%) than CL (8.1%). Biologic therapy was discontinued in 53.5%, leading to worsening of the underlying disease in 44.7%. No significant difference in cure rates was observed between patients who continued vs. discontinued biologics (p=0.868). These findings highlight the clinical burden of CL and MCL in patients undergoing anti-TNFα therapy and suggest that discontinuation of biologic therapy did not significantly impact cure rates, emphasizing the need for standardized strategies balancing infection control and underlying inflammatory disease management.
- 12 March 2026
- Published by Medical Journals Sweden AB in Acta Dermato-Venereologica
- Vol. 106
Open AccessCutaneous Leishmaniasis in Patients under Biologic Therapies: A Spanish CLINI-AEDV Multicentre Study
Anti-TNFα agents have been associated with the reactivation of granulomatous infections, including leishmaniasis. Cases of atypical or recurrent cutaneous (CL) or mucocutaneous leishmaniasis (MCL) have been reported in patients on biologics. We conducted a retrospective analysis of a multicenter database to describe the clinical characteristics and management of CL and MCL in patients receiving biological therapy in an endemic area. Clinical features, diagnostics, therapies, and outcomes were analyzed. Seventy-one patients were included (63 CL and 8 MCL). The most common underlying condition was inflammatory bowel disease (33.8%). Lesions were multifocal in 40% and larger than 1 cm in 94.4%. Treatment failures were more frequent in MCL (50%) than CL (8.1%). Biologic therapy was discontinued in 53.5%, leading to worsening of the underlying disease in 44.7%. No significant difference in cure rates was observed between patients who continued vs. discontinued biologics (p=0.868). These findings highlight the clinical burden of CL and MCL in patients undergoing anti-TNFα therapy and suggest that discontinuation of biologic therapy did not significantly impact cure rates, emphasizing the need for standardized strategies balancing infection control and underlying inflammatory disease management.