Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2015 Jul-Sep;10(3):287-9.
doi: 10.4103/1817-1745.165727.

Fatal cerebellar hemorrhage as an initial presentation of medulloblastoma in a child

Affiliations
Case Reports

Fatal cerebellar hemorrhage as an initial presentation of medulloblastoma in a child

Guner Menekse et al. J Pediatr Neurosci. 2015 Jul-Sep.

Abstract

Children with medulloblastomas most commonly present with signs and symptoms of elevated intracranial pressure due to obstructive hydrocephalus, especially headaches and vomiting. However, some pediatric patients present with sudden neurological deterioration due to intracerebellar hemorrhage associated with medulloblastoma, although very few reports exist that document this phenomenon. An 8-year-old girl was admitted to our emergency department who presented with sudden loss of consciousness, vomiting, and bradycardia. The neuroradiological evaluation revealed a hemorrhagic mass lesion in the posterior fossa. Urgent evacuation of the hematoma was performed. The postoperative course was uneventful, and the postoperative histopathological examination revealed the lesion to be a medulloblastoma. This report presents an unusual case of a medulloblastoma presenting with fatal intracranial hemorrhage in a child. The clinical features and intraoperative and pathologic findings of the case are discussed.

Keywords: Cerebellar hemorrhage; childhood; medulloblastoma.

PubMed Disclaimer

Figures

Figure 1
Figure 1
(a) Computerized tomography scan of the brain performed at admission, showing intracerebellar hemorrhage. (b) Postoperative computerized tomography image reveals successful evacuation of the lesion
Figure 2
Figure 2
Histological examination of the resected hemorrhagic mass. (a) Necrotic and hemorrhagic tumor tissue consistent with medulloblastoma (H and E, ×40). (b) Highly cellular tumor tissue was composed of primitive neuroepithelial cells; necrosis was present (H and E, ×100). (c) Numerous tumor cell nuclei stained positive with the Ki-67 monoclonal antibody (Anti-Ki-67, ×400)

Similar articles

Cited by

References

    1. Illinois, USA: Central Brain Tumor Registry of the United States; 2004-2005. CBTRUS. Statistical Report: (2004-2005), Primary Brain Tumors in the United States, 1997-2001.
    1. Santi M, Kadom N, Vezina G, Rushing EJ. Undiagnosed medulloblastoma presenting as fatal hemorrhage in a 14-year-old boy: Case report and review of the literature. Childs Nerv Syst. 2007;23:799–805. - PubMed
    1. Furuhata M, Aihara Y, Eguchi S, Horiba A, Tanaka M, Komori T, et al. Pediatric medulloblastoma presenting as cerebellar hemorrhage: A case report. No Shinkei Geka. 2014;42:545–51. - PubMed
    1. Elgamal EA, Richards PG, Patel UJ. Fatal haemorrhage in medulloblastoma following ventricular drainage. Case report and review of the literature. Pediatr Neurosurg. 2006;42:45–8. - PubMed
    1. Chugani HT, Rosemblat AM, Lavenstein BL, Palumbo FM, Luessenhop AJ, Manz HJ. Childhood medulloblastoma presenting with hemorrhage. Childs Brain. 1984;11:135–40. - PubMed

Publication types