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累及跗管内所有屈肌腱的广泛性滑膜软骨瘤病:一例报告

Extensive Synovial Chondromatosis Involving All Flexor Tendons in the Tarsal Tunnel: A Case Report.

作者信息

Pinter Zachariah, Shah Ashish, Netto Cesar de Cesar, Smith Walter, O'Daly Andres, Godoy-Santos Alexandre Leme

机构信息

Divisão de Cirurgia Ortopédica, Departamento de Cirurgia, University of Alabama, Birmingham, Estado Unidos.

Faculdade de Medicina, Departamento de Ortopedia, Universidade de São Paulo, São Paulo, SP, Brasil.

出版信息

Rev Bras Ortop (Sao Paulo). 2019 Feb;54(1):78-82. doi: 10.1016/j.rboe.2017.07.012. Epub 2019 Mar 1.

Abstract

Synovial chondromatosis is a rare condition characterized by benign chondrogenic meta- plasia of extra-articular synovial tissue. It usually affects a single tendon sheath of the hand or foot. This report describes a rare case with extensive synovial chondromatosis affecting all flexor tendons in the tarsal tunnel, its radiological features, surgical treatment, and clinical outcome. The authors present a unique case of extensive synovial chondromatosis in a 48-year-old male involving the tendon sheaths of the flexor hallucis longus, flexor digitorum longus, and posterior tibialis tendons, at the level of the tarsal tunnel, with extension into the plantar aspect of the foot. The patient initially presented with symptoms of tarsal tunnel compression and was found to have a 4-cm mass in the posteromedial aspect of the ankle. The presumptive diagnosis of synovial chondromatosis was made based on radiographic and magnetic resonance imaging evidence. The patient underwent surgical resection of the tumor, as well as tarsal tunnel release and gastrocnemius recession. The diagnosis was confirmed postoperatively by surgical histopathology. The postoperative course of the patient was uncomplicated and his tarsal tunnel symptoms resolved. This represents a case of extensive synovial chondromatosis involving all flexor tendons in the tarsal tunnel that was correctly diagnosed by clinical and imaging findings, which required early surgical resection to avoid long-term neurovascular complications.

摘要

滑膜软骨瘤病是一种罕见的疾病,其特征为关节外滑膜组织的良性软骨化生。它通常累及手部或足部的单个腱鞘。本报告描述了一例罕见的广泛滑膜软骨瘤病病例,该病例累及跗管内的所有屈肌腱,介绍了其放射学特征、手术治疗及临床结果。作者呈现了一例独特的广泛滑膜软骨瘤病病例,患者为一名48岁男性,病变累及跗管水平的拇长屈肌腱、趾长屈肌腱和胫后肌腱的腱鞘,并延伸至足底。患者最初表现为跗管受压症状,在踝关节后内侧发现一个4厘米的肿块。根据放射学和磁共振成像证据做出滑膜软骨瘤病的初步诊断。患者接受了肿瘤手术切除、跗管松解及腓肠肌松解术。术后手术组织病理学证实了诊断。患者术后病程顺利,跗管症状得以缓解。这是一例广泛滑膜软骨瘤病累及跗管内所有屈肌腱的病例,通过临床和影像学检查得以正确诊断,需要早期手术切除以避免长期神经血管并发症。

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