Behcet syndrome: A rare cause of recurrent genital ulceration.

IF 0.6 Q4 INFECTIOUS DISEASES
Sanya Kamal Narang, Hiral A Shah
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引用次数: 0

Abstract

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.

白歇综合征:一种罕见的原因,反复生殖器溃疡。
白塞综合征(BS)是一种慢性复发的多系统血管炎,其皮肤表现与遗传学有重要关系。在这里,我们提出一个16岁的男性的情况下,抱怨复发性生殖器,口腔溃疡与皮肤病变和静脉穿刺部位复发血栓性静脉炎的历史。无系统性表现。病理检查、HLA-B51均为阴性。根据BS的国际白塞病标准(ICBD)确诊。逐渐减少系统性皮质类固醇和秋水仙碱的剂量显示出良好的反应和病变的消退。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.60
自引率
25.00%
发文量
34
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