Ependymoma Presenting as a -Rim-Enhancing Lesion in the Brainstem.


Journal

Pediatric neurosurgery
ISSN: 1423-0305
Titre abrégé: Pediatr Neurosurg
Pays: Switzerland
ID NLM: 9114967

Informations de publication

Date de publication:
2021
Historique:
received: 04 12 2020
accepted: 18 03 2021
pubmed: 21 6 2021
medline: 29 10 2021
entrez: 20 6 2021
Statut: ppublish

Résumé

The posterior fossa is the most common intracranial location for pediatric ependymoma. While ependymoma usually arises from the ventricular lining of the fourth ventricle as a solid mass, it rarely originates from the brainstem. Grade II ependymomas also infrequently appear as a cavitary ring-enhancing lesion. We describe a case of a 6-year-old boy with an ependymoma arising within the medulla with imaging features of a thick-walled rim-enhancing cavitary lesion. A stereotactic biopsy was obtained which confirmed a grade II ependymoma. The patient received focal proton beam radiation therapy and is doing well with no concerns for disease progression at 28 months after diagnosis. Posterior fossa ependymomas typically arise from ependymal cells within the fourth ventricle or foramina of Luschka. They rarely invade or arise within the brainstem parenchyma. Our case had atypical imaging findings in addition to the atypical tumor location. The lesion was described as a thick-walled rim-enhancing focal cystic necrotic lesion centered within the medulla with surrounding nonenhancing expansile infiltrative changes. Ring-enhancing lesions can be seen in patients with anaplastic ependymoma, but is not commonly reported in grade II ependymomas. In summary, this report highlights a unique case of a posterior fossa ependymoma in a pediatric patient arising in an atypical brainstem location as well as having unique imaging features.

Identifiants

pubmed: 34148044
pii: 000516001
doi: 10.1159/000516001
doi:

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

455-459

Informations de copyright

© 2021 S. Karger AG, Basel.

Auteurs

Fatema Malbari (F)

Division of Neurology and Developmental Neurosciences, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas, USA.

Guillermo Aldave (G)

Division of Neurosurgery, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas, USA.

Sherri B Birchansky (SB)

Edward B. Singleton Department of Radiology, Texas Children's Hospital, Houston, Texas, USA.

Arnold C Paulino (AC)

Division of Radiation Oncology, Department of Radiation Oncology, MD Anderson Cancer Center, Houston, Texas, USA.

Dolores H Lopez-Terrada (DH)

Deparment of Pathology and Immunology, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas, USA.

Carrie A Mohila (CA)

Deparment of Pathology and Immunology, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas, USA.

Sibo Zhao (S)

Hematology and Oncology Center, Neuro-Oncology Program, Cook Children's Hospital, Fort Worth, Texas, USA.

Murali Chintagumpala (M)

Department of Pediatrics, Texas Children's Cancer Center, Baylor College of Medicine, Houston, Texas, USA.

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Classifications MeSH