Tenosynovial Giant Cell Tumor masked as de Quervain Tenosynovitis.

IF 0.7 4区 医学 Q4 ORTHOPEDICS
Q Diegenant, R Sciot, I Degreef
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引用次数: 0

Abstract

We present a patient who initially presented with clinical symptoms consistent with de Quervain tenosynovitis, resistant to conservative treatment. MRI revealed a cystic mass surrounding the radial styloid within the first extensor compartment (abductor pollicis longus (APL) and extensor pollicis brevis (EPB)), associated with scaphotrapezoid (STT) arthritis. However, upon surgical exploration, the lesion was identified as a localized tenosynovial giant cell tumor (TSGCT), which had caused erosion of the trapezium bone and compressed the EPB tendon. Histopathology confirmed the diagnosis. Postoperative recovery was uneventful, with functional improvement and no recurrence. This exceptional case highlights the importance of accurate diagnosis and the potential for atypical presentations of benign tumors. Informed consent was obtained from the patient after surgery to use her case details in publication for educational and research purposes.

腱鞘巨细胞瘤伪装成Quervain型腱鞘炎。
我们报告了一位患者,他最初的临床症状与de Quervain腱鞘炎一致,对保守治疗有抵抗力。MRI显示第一伸肌室(拇长外展肌(APL)和拇短伸肌(EPB))桡骨茎突周围有囊性肿块,与舟状锥体(STT)关节炎相关。然而,经手术探查,病变被确定为局限性腱鞘巨细胞瘤(TSGCT),该肿瘤导致斜方骨侵蚀并压迫EPB肌腱。组织病理学证实了诊断。术后恢复顺利,功能改善,无复发。这个特殊的病例强调了准确诊断的重要性和良性肿瘤的非典型表现的潜力。手术后获得患者的知情同意,将其病例细节用于教育和研究目的的出版物。
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来源期刊
Acta orthopaedica Belgica
Acta orthopaedica Belgica 医学-整形外科
CiteScore
0.70
自引率
0.00%
发文量
58
审稿时长
4-8 weeks
期刊介绍: Information not localized
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