JPA (Juvenile Pilocytic Astrocytoma)

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About JPA (Juvenile Pilocytic Astrocytoma)

General Information

  • Juvenile pilocytic astrocytomas (Grade 1 astrocytoma) occur more commonly in children and young adults. They also have a more favorable prognosis compared with all other astrocytoma types.
  • The most common site of juvenile pilocytic astrocytomas is the cerebellum.

Symptoms

  • The most common symptoms are headache, nausea, vomiting, poor balance and visual complaints, depending on the tumor site.
  • Many symptoms may be due to hydrocephalus.

Diagnosis

  • Magnetic resonance imaging (MRI) is the preferred imaging technique for diagnosis.
  • An actual tissue biopsy is typically required for definitive diagnosis in nearly all cases. If the tumor is inaccessible to open surgery, precisely guided (stereotactic) needle biopsies can be performed.

Treatment

  • Your UCLA neurosurgeon will determine with you how much of the tumor can or should be removed.
    • If the tumor is surgically accessible, a "complete" removal is attempted. This can be curative.
    • If the tumor is surgically inaccessible, a conservative, non-operative approach is recommended.
  • For surgical planning, mapping of critical speech and motor brain regions that may be adjacent to the tumor may be necessary. Such mapping is performed at the world-renowned UCLA Brain Mapping Center.
  • Often, juvenile pilocytic astrocytomas are best removed with the aid of intra-operative MRI, allowing the most complete, safest surgery possible.
Juvenile Pilocytic Imaging

 

This MRI image shows a juvenile pilocytic astrocytoma in the ventricle of the left frontal lobe (arrow). This patient had a partial removal of the tumor because the tumor involved the optic nerves.

 

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