| Literature DB >> 31076816 |
Robin Reschke1, Marketa Kadlecova2, Sonja Grunewald2, Mirjana Ziemer2.
Abstract
The case of segmental neurofibromatosis (NF) with a monstrous plexiform neurofibroma in a 53-year-old female patient is described. Segmental NF is a rare form of NF, which is caused by a postzygotic mutation in the NF1 gene. In this mosaic form the typical cutaneous symptoms of NF are limited to certain unilateral dermatomes. Plexiform neurofibromas are clinically and histologically in contrast to locally delimited neurofibromas. They involve the catchment area of a peripheral nerve, affect many fascicles and nerve branches, do not respect growth limits and spread in a reticulated fashion. Plexiform neurofibromas can become malignant. In the presented case large parts of the monstrous plexiform cutaneous neurofibroma were excised and the patient did not wish any further measures to be carried out for the time being.Entities:
Keywords: Excision; Mosaicism; Mutation; Neurodegenerative diseases; Peripheral nervous system neoplasms
Mesh:
Year: 2019 PMID: 31076816 DOI: 10.1007/s00105-019-4419-3
Source DB: PubMed Journal: Hautarzt ISSN: 0017-8470 Impact factor: 0.751