Nerve Tumors of the Hand and Forearm
Overview
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Peripheral nerve tumors comprise less than 5% of all tumors of the hand. The most common solitary nerve tumor is the neurilemmoma, which arises from the neural sheath, is well encapsulated, minimally symptomatic, and may be surgically enucleated without producing a neurological deficit. Neurofibromas may be solitary, multiple, or associated with von Recklinghausen's disease. They are usually centrally placed with nerve fibers traversing the tumor mass making it more difficult to remove the tumor without producing permanent neurological damage. Malignant tumors include neurofibrosarcomas which often are very aggressive, requiring wide excision or amputation, and the rare neuroepitheliomas. Reported nerve tumors, intraneural in location but nonneural in origin, include fibrofatty infiltration of the median and digital nerves, intraneural lipoma, hemangioma, and ganglion cysts. These lesions may be treated by decompression or excision, depending on the nature of the tumor. Four unusual cases are described.
Neurofibroma Involving a Bifid Median Nerve in a Pediatric Patient: A Case Report.
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PMID: 38903847 PMC: 11185877. DOI: 10.1016/j.jhsg.2023.12.001.
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Diffuse Type Neurofibroma of the Forearm.
Al Lahham S, Aljassem G, Omari R, Alyazji Z, Sada R, Asnaf A Plast Reconstr Surg Glob Open. 2022; 10(5):e4341.
PMID: 35620496 PMC: 9126514. DOI: 10.1097/GOX.0000000000004341.
Schwannoma in the extremity: clinical features and microscopic intra-capsular enucleation.
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PMID: 34707726 PMC: 8527622. DOI: 10.2185/jrm.2021-020.
Multiple Schwannomas of the Median Nerve: A Case Report and Review of the Literature.
Salar M, Kaye M J Orthop Case Rep. 2021; 10(6):60-63.
PMID: 33489971 PMC: 7815672. DOI: 10.13107/jocr.2020.v10.i06.1876.