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Ependymoma Presenting as a -Rim-Enhancing Lesion in the Brainstem.
Malbari, Fatema; Aldave, Guillermo; Birchansky, Sherri B; Paulino, Arnold C; Lopez-Terrada, Dolores H; Mohila, Carrie A; Zhao, Sibo; Chintagumpala, Murali.
Afiliación
  • Malbari F; Division of Neurology and Developmental Neurosciences, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas, USA.
  • Aldave G; Division of Neurosurgery, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas, USA.
  • Birchansky SB; Edward B. Singleton Department of Radiology, Texas Children's Hospital, Houston, Texas, USA.
  • Paulino AC; Division of Radiation Oncology, Department of Radiation Oncology, MD Anderson Cancer Center, Houston, Texas, USA.
  • Lopez-Terrada DH; Deparment of Pathology and Immunology, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas, USA.
  • Mohila CA; Deparment of Pathology and Immunology, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas, USA.
  • Zhao S; Hematology and Oncology Center, Neuro-Oncology Program, Cook Children's Hospital, Fort Worth, Texas, USA.
  • Chintagumpala M; Department of Pediatrics, Texas Children's Cancer Center, Baylor College of Medicine, Houston, Texas, USA.
Pediatr Neurosurg ; 56(5): 455-459, 2021.
Article en En | MEDLINE | ID: mdl-34148044
INTRODUCTION: 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. CASE PRESENTATION: 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. CONCLUSION: 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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ependimoma / Terapia de Protones Límite: Child / Humans / Male Idioma: En Revista: Pediatr Neurosurg Asunto de la revista: NEUROCIRURGIA / PEDIATRIA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ependimoma / Terapia de Protones Límite: Child / Humans / Male Idioma: En Revista: Pediatr Neurosurg Asunto de la revista: NEUROCIRURGIA / PEDIATRIA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos