Astrocytomas

From WikiMD's Wellness Encyclopedia

Astrocytomas

Astrocytomas are a type of brain tumor that originate from astrocytes, which are star-shaped glial cells in the brain and spinal cord. These tumors are a subset of gliomas, which are tumors that arise from glial cells. Astrocytomas can occur in various parts of the brain and spinal cord and can vary greatly in their behavior and prognosis.

Classification[edit | edit source]

Astrocytomas are classified based on their histological features and their grade, which reflects their aggressiveness. The World Health Organization (WHO) grading system is commonly used:

  • Grade I: Pilocytic Astrocytoma
 * These are typically benign and slow-growing tumors, often found in children and young adults. They are usually well-circumscribed and can often be cured with surgical resection.
  • Grade II: Diffuse Astrocytoma
 * These tumors are infiltrative and have a tendency to progress to higher-grade tumors over time. They are considered low-grade but are more challenging to treat than Grade I tumors.
  • Grade III: Anaplastic Astrocytoma
 * These are malignant tumors that grow more rapidly and are more aggressive than Grade II astrocytomas. They often require a combination of surgery, radiation, and chemotherapy.
  • Grade IV: Glioblastoma
 * Also known as glioblastoma multiforme (GBM), these are the most aggressive and common form of astrocytoma. They are highly malignant, with a poor prognosis despite aggressive treatment.

Symptoms[edit | edit source]

The symptoms of astrocytomas depend on the tumor's location, size, and rate of growth. Common symptoms include:

  • Headaches
  • Seizures
  • Neurological deficits (e.g., weakness, sensory changes)
  • Cognitive or personality changes
  • Nausea and vomiting

Diagnosis[edit | edit source]

Diagnosis of astrocytomas typically involves a combination of imaging studies and biopsy:

  • Magnetic Resonance Imaging (MRI)
 * MRI is the preferred imaging modality for brain tumors, providing detailed images of the brain and spinal cord.
  • Biopsy
 * A biopsy is often necessary to obtain a definitive diagnosis and to determine the tumor's grade.

Treatment[edit | edit source]

Treatment strategies for astrocytomas depend on the tumor's grade and location:

  • Surgery
 * Surgical resection is often the first step in treatment, aiming to remove as much of the tumor as possible.
  • Radiation Therapy
 * Radiation is commonly used post-surgery, especially for higher-grade tumors.
  • Chemotherapy
 * Chemotherapy may be used in conjunction with radiation, particularly for anaplastic astrocytomas and glioblastomas.

Prognosis[edit | edit source]

The prognosis for patients with astrocytomas varies widely based on the tumor's grade and the patient's age and overall health. Pilocytic astrocytomas generally have an excellent prognosis, while glioblastomas have a median survival of approximately 15 months despite treatment.

Also see[edit | edit source]


Resources[edit source]

Latest articles - Astrocytomas

PubMed
Clinical trials

Source: Data courtesy of the U.S. National Library of Medicine. Since the data might have changed, please query MeSH on Astrocytomas for any updates.


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Contributors: Prab R. Tumpati, MD