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Published in: Brain Tumor Pathology 1/2014

01-01-2014 | Case Report

Intradural extramedullary spinal nerve sheath myxoma: a report of two cases

Authors: Mariko Yamato, Hayato Ikota, Junya Hanakita, Yoichi Iizuka, Yoichi Nakazato

Published in: Brain Tumor Pathology | Issue 1/2014

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Abstract

Nerve sheath myxoma, a myxoid variant of schwannoma, is a dermal tumor that usually occurs in the upper extremities, head and neck region, or trunk; occasionally, however, it has also been reported to develop in the spinal canal. Here, we describe two cases of intraspinal nerve sheath myxoma. Case 1 was a 74-year-old man with left hypochondrial pain. Gadolinium-enhanced magnetic resonance imaging (MRI) of his spine revealed a well-demarcated intradural extramedullary tumor with peripheral enhancement at the Th8 level. Case 2 was a 58-year-old man with lower back and left buttock pain. Gadolinium-enhanced MRI revealed a well-demarcated intradural extramedullary tumor with peripheral enhancement at the Th12-L1 level. Both cases were clinically diagnosed as schwannoma. Histological studies revealed characteristic myxoid lobules which were separated by fibrous septa or bands of more compact cellular area. The tumor cells were diffusely positive for S-100 and focally positive for Schwann/2E, which reacts with Schwann cells and myelin in the peripheral nervous system. The positive reaction to Schwann/2E confirmed the occurrence of peripheral nerve sheath differentiation. Nerve sheath myxoma should be included in differential diagnosis of spinal canal tumors.
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Metadata
Title
Intradural extramedullary spinal nerve sheath myxoma: a report of two cases
Authors
Mariko Yamato
Hayato Ikota
Junya Hanakita
Yoichi Iizuka
Yoichi Nakazato
Publication date
01-01-2014
Publisher
Springer Japan
Published in
Brain Tumor Pathology / Issue 1/2014
Print ISSN: 1433-7398
Electronic ISSN: 1861-387X
DOI
https://doi.org/10.1007/s10014-012-0131-z

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