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{{Medulloblastoma}}
{{Medulloblastoma}}
{{CMG}}
{{CMG}} {{AE}}{{HL}}
==Overview==
==Overview==
==Natural History==
==Natural History==

Revision as of 23:35, 28 September 2015

Medulloblastoma Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Medulloblastoma from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Staging

History and Symptoms

Physical Examination

Laboratory Findings

CT

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case studies

Case #1

Medulloblastoma natural history On the Web

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FDA on Medulloblastoma natural history

CDC on Medulloblastoma natural history

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Blogs on Medulloblastoma natural history

Directions to Hospitals Treating Medulloblastoma

Risk calculators and risk factors for Medulloblastoma natural history

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Haytham Allaham, M.D. [2]

Overview

Natural History

Complications

Prognosis

Treatment begins with maximal resection of the tumor. The addition of radiation to the entire neuraxis and chemotherapy may increase the disease-free survival. This combination may permit a 5 year survival in more than 80% of cases. The presence of desmoplastic features such as connective tissue formation offers a better prognosis. Prognosis is worse if child is less than 3 years old, inadequate degree of resection, or if presence of any CSF, spinal, supratentorial or systemic spread.

Increase intracranial pressure may be controlled with corticosteroids or a ventriculoperitoneal shunt

References


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