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Neurotropic melanoma. A case report and review of the literature.

作者信息

Mack E E, Gomez E C

机构信息

Department of Neurology, Cornell University Medical Center, New York, NY.

出版信息

J Neurooncol. 1992 Jun;13(2):165-71. doi: 10.1007/BF00172766.

DOI:10.1007/BF00172766
PMID:1331344
Abstract

Neurotropic melanoma is a rare tumor with a biphasic growth pattern associated with a change in morphology from melanocytic features toward Schwann cell features. The tumor thereby develops a capacity for infiltrating nerves which may result in clinically evident cranial neuropathies, most commonly of the fifth and seventh cranial nerves. The histology of this lesion is difficult to interpret; it often erroneously appears fibrous in origin and may be considered to be benign. Despite this benign appearance histologically, the tumor behaves aggressively with multiple local recurrences and possible CNS invasion by either direct perineural growth or distant metastases. We review the literature of neurotropic melanomas and report a 46th case which describes a typical course with neural invasion. Although a rare cause of cranial neuropathies, the neurologist should consider this entity in the differential diagnosis and the history of a recurrent skin lesion of the face should be sought whenever examining such a patient.

摘要

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[Desmoplastic neurotropic melanoma. Diagnosis and therapeutic procedures for a rare clinical entity].

本文引用的文献

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10
Neurotropic melanoma of the head and neck.头颈部亲神经性黑色素瘤
Laryngoscope. 1985 Oct;95(10):1161-6. doi: 10.1288/00005537-198510000-00002.