Articular flare-up of systemic scleroderma revealing a rare form of tuberculosis of the shoulder and extensor tendons: a case report and literature review.

Access microbiology Pub Date : 2025-10-01 eCollection Date: 2025-01-01 DOI:10.1099/acmi.0.001023.v3
H Zouaki, H Laatiris, L Taoubane, A Mejjad, H Toufik, N Elouardi, A Bezza
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引用次数: 0

Abstract

Tuberculosis remains a major public health concern, particularly in countries where it is still endemic. Tuberculous bursitis and tenosynovitis are rare extrapulmonary manifestations, and their association with systemic autoimmune diseases such as scleroderma is seldom reported in the literature. We report the case of a 61-year-old patient with systemic scleroderma, complicated by diffuse interstitial lung disease and treated with mycophenolate mofetil, who developed tuberculous shoulder bursitis and wrist extensor tenosynovitis. The microbiological diagnosis was confirmed by ultrasound-guided aspiration of the subacromial-subdeltoid bursa, revealing the presence of Mycobacterium tuberculosis, detected by Ziehl-Neelsen staining, GeneXpert PCR and culture. Histological analysis of synovial tissue fragments demonstrated epithelioid granulomas with caseous necrosis, confirming the tuberculous origin.

关节突发的系统性硬皮病揭示一种罕见形式的结核肩和伸肌腱:一个病例报告和文献复习。
结核病仍然是一个主要的公共卫生问题,特别是在结核病仍然流行的国家。结核性滑囊炎和腱鞘炎是罕见的肺外表现,它们与硬皮病等系统性自身免疫性疾病的关联在文献中很少报道。我们报告一例61岁的系统性硬皮病患者,并发弥漫性间质性肺病,经霉酚酸酯治疗,并发结核性肩滑囊炎和腕伸肌腱鞘炎。超声引导下滴注肩峰下-三角下滑囊证实微生物学诊断,发现结核分枝杆菌存在,Ziehl-Neelsen染色,GeneXpert PCR和培养检测。滑膜组织碎片的组织学分析显示上皮样肉芽肿伴干酪样坏死,证实结核起源。
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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