Lipofibromatous Hamartoma of the Median and Ulnar Nerves: A Case Report.

Patricio A Alfaro, Lucas G Silva, Marion E Hohf
{"title":"Lipofibromatous Hamartoma of the Median and Ulnar Nerves: A Case Report.","authors":"Patricio A Alfaro, Lucas G Silva, Marion E Hohf","doi":"10.13107/jocr.2026.v16.i10.8202","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Lipofibromatous hamartoma (LFH) is a rare, benign tumor of peripheral nerves characterized by fibroadipose infiltration of the epineurium and perineurium. It most frequently involves the median nerve and is rarely seen with concomitant ulnar nerve involvement.</p><p><strong>Case report: </strong>We report a 28-year-old male with a 13-year history of a slowly progressive mass over the volar aspect of the left hand and wrist, associated with persistent hypoesthesia in the thumb and intermittent paresthesia in the ring and little fingers. Magnetic resonance imaging (MRI) revealed the pathognomonic \"coaxial cable\" and \"spaghetti\" signs involving both the median and ulnar nerves. The patient underwent extended neurolysis of both nerves with carpal tunnel and Guyon's canal release. Histopathology confirmed LFH without atypia. At 12-month follow-up, he showed sustained improvement in pain and sensory symptoms, with complete return to work.</p><p><strong>Conclusion: </strong>Concomitant LFH of the median and ulnar nerves is extremely rare. MRI provides pathognomonic diagnosis, and extended neurolysis without tumor resection can achieve favorable functional outcomes.</p>","PeriodicalId":16647,"journal":{"name":"Journal of Orthopaedic Case Reports","volume":"16 10","pages":"103-105"},"PeriodicalIF":0.0000,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13646467/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Orthopaedic Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.13107/jocr.2026.v16.i10.8202","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Lipofibromatous hamartoma (LFH) is a rare, benign tumor of peripheral nerves characterized by fibroadipose infiltration of the epineurium and perineurium. It most frequently involves the median nerve and is rarely seen with concomitant ulnar nerve involvement.

Case report: We report a 28-year-old male with a 13-year history of a slowly progressive mass over the volar aspect of the left hand and wrist, associated with persistent hypoesthesia in the thumb and intermittent paresthesia in the ring and little fingers. Magnetic resonance imaging (MRI) revealed the pathognomonic "coaxial cable" and "spaghetti" signs involving both the median and ulnar nerves. The patient underwent extended neurolysis of both nerves with carpal tunnel and Guyon's canal release. Histopathology confirmed LFH without atypia. At 12-month follow-up, he showed sustained improvement in pain and sensory symptoms, with complete return to work.

Conclusion: Concomitant LFH of the median and ulnar nerves is extremely rare. MRI provides pathognomonic diagnosis, and extended neurolysis without tumor resection can achieve favorable functional outcomes.

中尺神经脂肪纤维瘤错构瘤1例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
128
审稿时长
30 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书