Behcet syndrome: A rare cause of recurrent genital ulceration

Behcet syndrome (BS) is a chronic relapsing multisystem vasculitis with skin findings with an important contribution of genetics. Here, we present a case of a 16-year-old male with a complaint of recurrent genital, and oral ulceration with skin lesions and a history of recurrent thrombophlebitis at...

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Veröffentlicht in:Indian journal of sexually transmitted diseases 2024-07, Vol.45 (2), p.156-159
Hauptverfasser: Narang, Sanya Kamal, Shah, Hiral A
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Shah, Hiral A
description Behcet syndrome (BS) is a chronic relapsing multisystem vasculitis with skin findings with an important contribution of genetics. Here, we present a case of a 16-year-old male with a complaint of recurrent genital, and oral ulceration with skin lesions and a history of recurrent thrombophlebitis at the sites of venepuncture. There were no systemic manifestations. Pathergy test and HLA-B51 were negative. The diagnosis was confirmed based on the International Criteria for Behcet disease (ICBD) for BS. Tapering doses of systemic corticosteroid and colchicine showed promising response and regression of lesions.
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source PubMed Central Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Colchicine
Diagnosis
Diseases
Relapse
Skin
Skin lesions
title Behcet syndrome: A rare cause of recurrent genital ulceration
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