| Literature DB >> 31900294 |
Aisling Kelly1, Deirdre Nally2, Stephen Crowther3, Dara Kavanagh2.
Abstract
Ependymomas are neoplasms which arise from the radial glial cells, which many recent studies have proposed are neural stem cells. Extracranial ependymomas are rare. We present the case report and supporting multimedia of a 37-year-old man who presented with a painless intergluteal swelling which was diagnosed clinically as a pilonidal cyst. However, on excision, he was found to have a subcutaneous sacrococcygeal myxopapillary ependymoma based on histological findings. His management and follow-up are presented and discussed. Given the rare nature of this condition, there is a lack of published guidelines on management and follow-up protocols. Supporting evidence is limited to sporadic case reports. This case highlights the diagnostic challenges and management strategies adopted supported by the best available evidence. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: CNS cancer; general surgery; pathology
Mesh:
Year: 2020 PMID: 31900294 PMCID: PMC6954808 DOI: 10.1136/bcr-2019-231639
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X