Subcutaneous Sacrococcygeal Myxopapillary Ependymoma
Overview
Authors
Affiliations
We report an 8-year-old boy with a primary subcutaneous sacrococcygeal ependymoma, a rare tumor that is thought to arise in embryologic rests. The lesion was completely removed in our patient, who has been followed without recurrence for 20 months. Our experience, together with that of the other 15 cases in the world literature, supports surgical excision as the mainstay of treatment.
Paediatric extra-axial myxopapillary ependymoma: what to expect? Case report and literature review.
Lo Piccolo R, Cianci M, Sardi I, Di Nicola M, Buccoliero A, Caporalini C Front Oncol. 2025; 15:1519842.
PMID: 39949744 PMC: 11821608. DOI: 10.3389/fonc.2025.1519842.
Pediatric Extraspinal Sacrococcygeal Ependymoma: Report of Two Cases and Literature Review.
Fabozzi F, Ceccanti S, Cacchione A, Colafati G, Carai A, Crocoli A Diagnostics (Basel). 2021; 11(9).
PMID: 34574021 PMC: 8471863. DOI: 10.3390/diagnostics11091680.
Surgical management of a rare myxopapillary ependymoma of the gluteal region: A case report.
Lien B, Brown N, Himstead A, Ball B, Guillen A, Acharya N Surg Neurol Int. 2021; 12:130.
PMID: 33880235 PMC: 8053468. DOI: 10.25259/SNI_768_2020.
Sofuoglu O, Abdallah A Med Sci Monit. 2018; 24:7072-7089.
PMID: 30287802 PMC: 6186154. DOI: 10.12659/MSM.910447.
Yoshioka K, Murakami H, Demura S, Kato S, Kawahara N, Tomita K Surg J (N Y). 2017; 1(1):e50-e53.
PMID: 28824973 PMC: 5530622. DOI: 10.1055/s-0035-1567878.