Craniopharyngiomas

Diagnosis

Craniopharyngioma is a rare type of brain tumor that develops near the pituitary gland. The diagnosis of craniopharyngioma typically involves a combination of imaging tests, such as MRI and CT scans, and neurological exams. Here are some tests and procedures that may be used to diagnose craniopharyngioma:

  • Physical examination: Healthcare provider will often analyze the medical history and perform a neurological examination before diagnosing the patient with a craniopharyngioma. The hearing, balance, coordination, reflexes, growth, and development are all examined during this examination.
  • Imaging test:
    • Magnetic Resonance Imaging (MRI): This imaging test uses a powerful magnet and radio waves to produce detailed images of the brain. It can help identify the location, size, and shape of the tumor.
    • Computed Tomography (CT) Scan: This imaging test uses X-rays to produce cross-sectional images of the brain. It can help identify the location and size of the tumor.
  • Hormone Tests: Since craniopharyngioma often affects the pituitary gland, hormone tests may be performed to check for hormonal imbalances.
  • Biopsy: In some cases, a biopsy may be performed to confirm the diagnosis of craniopharyngioma. This involves removing a small sample of the tumor tissue and examining it under a microscope.

It is important to note that the specific tests and procedures used to diagnose craniopharyngioma may vary depending on the individual case and the healthcare provider’s preferences.

Treatment

The treatment options for craniopharyngioma may depend on various factors such as the size and location of the tumor, the patient’s age and overall health, and the extent of the tumor’s invasion into surrounding tissue. Some treatment options for craniopharyngioma include:

  • Observation: In some cases, especially in elderly patients or those with small, slow-growing tumors, observation or “watchful waiting” may be an option. This involves monitoring the tumor’s growth over time with regular imaging tests and only treating it if it starts to cause symptoms or show signs of progression.
  • Surgery: Craniopharyngioma treatment typically involves surgical intervention to remove the majority, if not all, of the tumor. The surgical approach used depends on the size and location of the tumor. Open craniopharyngioma surgery involves opening the skull to access the tumor, while minimally invasive surgery involves inserting specialized tools through the nose to access the tumor without disturbing the brain. When possible, the goal of surgery is complete tumor removal. However, in some cases, the proximity of vital structures makes complete removal challenging. In such instances, surgeons may leave some of the tumor behind to preserve the patient’s quality of life. Other treatments may be used in conjunction with surgery.
  • Radiation therapy: After a craniopharyngioma surgery, external beam radiation therapy may be used to kill remaining tumor cells. X-rays and protons are used to deliver energy beams to the tumor cells, while sparing nearby healthy tissue. Advanced external beam radiation techniques such as proton beam therapy and intensity-modulated radiation therapy (IMRT) allow precise shaping and aiming of the radiation beam. In some cases where the optic nerve is not affected, a type of radiation therapy called stereotactic radiosurgery may be used, which focuses multiple beams of radiation on specific points to kill the tumor cells. Brachytherapy is another type of radiation therapy, where radioactive material is placed directly into the tumor to radiate it from the inside.
  • Chemotherapy: Chemotherapy is a medical procedure that involves the use of drugs to eliminate cancerous cells. By administering chemicals directly into the tumor, the treatment can effectively target the affected cells without causing harm to the surrounding healthy tissues.
  • Hormone replacement therapy: Since craniopharyngioma can disrupt the normal function of the pituitary gland and hypothalamus, hormone replacement therapy may be necessary to replace hormones that are not being produced adequately by these glands. This may involve taking medications to replace thyroid, adrenal, or growth hormones, among others.