Glomus-like bodies within a neurofibroma: a novel neoplasm arising in neurofibromatosis type 1 or a coincidence?

Abstract:

:Neurofibromatosis type 1 is a relatively common genetic disorder with variable phenotypes. Tumors with features of both glomus tumors and neurofibromas are exceedingly rare in literature. Herein, we report a not yet described neoplasm with features of both a glomangioma/glomus tumor and a neurofibroma arising in a patient with segmental neurofibromatosis. Our case report supports the theory of a common lineage/ancestor cell between neurofibromas and glomus tumors and adds it to the spectrum of neoplasms that may arise in the setting of Von Recklinghausen's disease.

journal_name

J Cutan Pathol

authors

Thareja S,Honigbaum A,Jukic D

doi

10.1111/cup.12439

subject

Has Abstract

pub_date

2015-04-01 00:00:00

pages

285-8

issue

4

eissn

0303-6987

issn

1600-0560

journal_volume

42

pub_type

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