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结核性复合性掌部腱鞘囊肿:揭示一种罕见诊断

Tuberculous compound palmar ganglion: unravelling a rare diagnosis.

作者信息

Jilani Latif Zafar, Istiyak Mohammad, Sudarshan Akash

机构信息

Department of Orthopaedic Surgery, J.N. Medical College, Faculty of Medicine, A.M.U Aligarh, India.

出版信息

Int J Burns Trauma. 2025 Apr 25;15(2):77-82. doi: 10.62347/ZYHQ5711. eCollection 2025.

Abstract

BACKGROUND

Tuberculous tenosynovitis is a rare manifestation of musculoskeletal tuberculosis, often misdiagnosed due to its indolent course and nonspecific presentation. Compound palmar ganglion, a chronic form of tuberculous tenosynovitis, can mimic benign conditions like ganglion cysts, leading to diagnostic delays, especially in immunocompromised individuals.

CASE REPORT

We report a case of a 35-year-old HIV-positive female who presented with a painless swelling on the volar aspect of the wrist for six months. MRI revealed flexor tendon thickening and synovial proliferation, raising suspicion of infectious tenosynovitis. Surgical excision was performed, and histopathological examination confirmed tuberculous tenosynovitis with caseous granulomas. Ziehl-Neelsen staining identified acid-fast bacilli, confirming the diagnosis. The patient was started on standard anti-tubercular therapy (ATT) and showed complete resolution of symptoms at six months.

CONCLUSION

Tuberculous compound palmar ganglion should be considered in chronic wrist swellings, particularly in endemic regions and immunocompromised patients. Early diagnosis using imaging and histopathology is crucial for timely management. A combination of surgical excision and ATT ensures favorable outcomes.

摘要

背景

结核性腱鞘炎是肌肉骨骼结核的一种罕见表现,因其病程隐匿且表现不具特异性,常被误诊。复合性掌部腱鞘囊肿是结核性腱鞘炎的一种慢性形式,可类似腱鞘囊肿等良性病变,导致诊断延误,在免疫功能低下个体中尤为如此。

病例报告

我们报告一例35岁的HIV阳性女性,其腕掌侧出现无痛性肿胀6个月。磁共振成像显示屈肌腱增厚和滑膜增生,怀疑为感染性腱鞘炎。进行了手术切除,组织病理学检查证实为结核性腱鞘炎伴干酪样肉芽肿。萋-尼染色发现抗酸杆菌,确诊。患者开始接受标准抗结核治疗(ATT),6个月时症状完全缓解。

结论

对于慢性腕部肿胀,尤其是在流行地区和免疫功能低下患者中,应考虑结核性复合性掌部腱鞘囊肿。利用影像学和组织病理学进行早期诊断对于及时治疗至关重要。手术切除与ATT联合应用可确保良好预后。

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