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一名患有巨指症的西班牙裔患者的脂肪纤维瘤性错构瘤:一种导致复发性腕管综合征的罕见周围神经肿瘤。

Lipofibromatous Hamartoma in a Hispanic Patient with macrodactyly: a rare peripheral nerve tumor causing recurrent carpal tunnel syndrome.

作者信息

Pinci Marcantonio V, Olivella Gerardo, Rodríguez Manuel, Hess-Arcelay Hans W, Ramírez Norman, Foy-Parilla Christian

机构信息

Orthopaedic Surgery Department University of Puerto Rico, Medical Sciences Campus San Juan, San Juan 00936-5067, Puerto Rico.

Pediatric Orthopaedic Surgery Department, Mayagüez Medical Center, Mayagüez 00681, Puerto Rico.

出版信息

J Surg Case Rep. 2020 Oct 31;2020(10):rjaa418. doi: 10.1093/jscr/rjaa418. eCollection 2020 Oct.

DOI:10.1093/jscr/rjaa418
PMID:33154809
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7602361/
Abstract

This is a rare case of a 42-year-old Hispanic male with macrodactyly who presented with recurrent carpal tunnel syndrome (CTS) due to Lipofibromatous Hamartoma (LFH). A slowly growing mass in his right palm with pain and numbness, along with motor and sensory deficits in the median nerve distribution, was reported since the past year prior to visit. Previous open carpal tunnel release was performed at 16 years of age due to CTS without complications. The diagnosis of LFH was made based on ultrasound, electromyography test and physical examination. An extended open carpal tunnel release with transection of transverse ligament was performed. The 24-month postoperative evaluation showed complete resolution of symptoms. This report illustrates the management of a recurrent CTS due to LFH in a Hispanic adult patient with macrodactyly that was successfully treated with a carpal tunnel decompression.

摘要

这是一例罕见的42岁西班牙裔男性巨指症患者,因脂肪纤维瘤性错构瘤(LFH)出现复发性腕管综合征(CTS)。自就诊前一年起,他的右手掌出现一个缓慢生长的肿块,伴有疼痛和麻木,同时正中神经分布区域存在运动和感觉功能障碍。患者16岁时曾因CTS接受过开放性腕管松解术,未出现并发症。LFH的诊断基于超声、肌电图检查和体格检查。实施了开放性腕管延长松解术并横断横韧带。术后24个月的评估显示症状完全缓解。本报告阐述了一名患有巨指症的西班牙裔成年患者因LFH导致复发性CTS的治疗情况,通过腕管减压术成功治愈。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8294/7602361/8624e842cb64/rjaa418f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8294/7602361/2686c28e2938/rjaa418f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8294/7602361/8624e842cb64/rjaa418f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8294/7602361/2686c28e2938/rjaa418f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8294/7602361/8624e842cb64/rjaa418f2.jpg

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Lipofibromatous Hamartoma in a Hispanic Patient with macrodactyly: a rare peripheral nerve tumor causing recurrent carpal tunnel syndrome.一名患有巨指症的西班牙裔患者的脂肪纤维瘤性错构瘤:一种导致复发性腕管综合征的罕见周围神经肿瘤。
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本文引用的文献

1
Carpal Tunnel Syndrome Caused by Lipofibromatous Hamartoma of the Median Nerve.正中神经脂肪纤维瘤性错构瘤导致的腕管综合征
J Korean Neurosurg Soc. 2020 Sep;63(5):664-670. doi: 10.3340/jkns.2020.0082. Epub 2020 Jun 29.
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Use of Ultra-high-frequency Ultrasound on Diagnosis and Management of Lipofibromatous Hamartoma: A Technical Report.超高频超声在脂肪纤维瘤性错构瘤诊断与治疗中的应用:技术报告
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Lipofibromatous Hamartoma of the Palmar Cutaneous Branch of the Median Nerve.
正中神经掌皮支的脂肪纤维瘤性错构瘤
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Lipofibromatous hamartoma of the median nerve: a comprehensive review and systematic approach to evaluation, diagnosis, and treatment.正中神经脂肪纤维瘤性错构瘤:评估、诊断及治疗的全面综述与系统方法
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Recurrent carpal tunnel syndrome in a child due to fibrolipomatous hamartoma of the median nerve successfully treated by limited excision and decompression.一名儿童因正中神经纤维脂肪性错构瘤导致复发性腕管综合征,经有限切除和减压成功治疗。
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Lipofibromas of the median nerve: long-term follow-up of four cases.
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