Muscle involvement in Behçet's syndrome: a case report.

IF 2.7
M Ma, F Fang, L Zhao, J Jin, Y Cheng
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引用次数: 0

Abstract

Behçet's syndrome, a systemic vasculitis of unknown aetiology, is classically characterized by recurrent aphthous ulcers, genital ulcers, uveitis, and cutaneous lesions. Myositis in Behçet's syndrome is rare. A unique case of Behçet's syndrome with gastrocnemius and tongue myositis as the presenting manifestations is presented here. The patient was admitted with fever, recurrent aphthous ulcers, and swelling and pain of the tongue and legs. Phlebitis of the deep-tissue vessels was seen in the tongue biopsy. A gastrocnemius muscle biopsy showed obvious muscle fibre degeneration, accompanied by swelling of the vascular endothelial cells with abundant lymphocytic infiltration. After treatment with prednisone and thalidomide, the swelling of the tongue and legs was reduced. Therefore, in the case of recurrent oral ulcers accompanied by fever and muscle lesions, even in the absence of clinical findings such as genital ulcers or ophthalmitis, it is necessary to be alert to the possibility of Behçet's syndrome.

behaperet综合征肌肉受累1例报告。
behet综合征是一种病因不明的全身性血管炎,其典型特征为复发性口腔溃疡、生殖器溃疡、葡萄膜炎和皮肤病变。肌炎在behet综合征是罕见的。本文报告一例以腓肠肌和舌肌炎为主要表现的behaperet综合征。患者入院时伴有发热、口疮复发、舌部和腿部肿痛。舌部活检可见深部组织血管炎。腓肠肌活检显示明显的肌纤维变性,血管内皮细胞肿胀伴大量淋巴细胞浸润。经强的松和沙利度胺治疗后,舌部和腿部肿胀减轻。因此,在复发性口腔溃疡伴有发热和肌肉病变的情况下,即使没有生殖器溃疡或眼炎等临床表现,也要警惕behet综合征的可能性。
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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