Deen Alsalman
StoryYearsZeldaSmashMarioMinecraftCancersBrain TumoursContactLinks

Share this page

Craniopharyngioma

A benign tumor found near the pituitary gland.

Location

Suprasellar region

Histological Classification

Non-glial


Details

Origin: Embryonic tissue

Grade: I

Severity: Low

Molecular Marker: CTNNB1 mutation

Age Range: 5-14 years

Life Expectancy: 20+ years

Lifespan Impact

Summary

Craniopharyngioma is a type of non-glial brain tumor that typically arises in the suprasellar region, which is located near the pituitary gland at the base of the brain. It is generally a slow-growing, benign tumor but can cause significant health issues due to its location.

Symptoms

Symptoms of craniopharyngioma can vary depending on the size and exact location of the tumor. Common symptoms include:

  • Headaches: Often due to increased pressure within the skull.
  • Vision Problems: Due to compression of the optic nerves.
  • Hormonal Imbalances: Resulting from pituitary dysfunction, leading to conditions such as diabetes insipidus, growth hormone deficiency, hypothyroidism, and adrenal insufficiency.
  • Fatigue and Sleep Disturbances: Often linked to hormonal changes.
  • Behavioral Changes: Including mood swings and cognitive difficulties.
  • Nausea and Vomiting: Caused by increased intracranial pressure.

Surgical Intervention

  • Traditional Surgery: The primary treatment for craniopharyngioma is often surgical removal. This can be challenging due to the tumor's proximity to critical brain structures.
  • Endoscopic Endonasal Surgery: A minimally invasive approach through the nasal cavity, which has become more common in recent years (widespread use since the 2000s).

Risks

  • Neurological Damage: Risk of damage to surrounding brain tissue, potentially affecting vision, hormone balance, and cognition.
  • Infection and Bleeding: Standard surgical risks.

Radiation Therapy

  • Conventional Radiation: Often used post-surgery to help prevent recurrence.
  • Proton Beam Therapy: A more targeted form of radiation that reduces damage to surrounding healthy tissue. This has been available since the early 2000s and is increasingly used due to its precision.

Risks

  • Cognitive Decline: Long-term effects on memory and cognitive function.
  • Secondary Tumors: A small risk of developing other tumors due to radiation exposure.

Medication

  • Hormone Replacement Therapy: Necessary for managing hormonal imbalances caused by the tumor or its treatment.

  • Side Effects: Weight gain, mood swings, fatigue, and other symptoms related to hormonal changes.

Targeted Molecular Therapy

  • BRAF Inhibitors: Some craniopharyngiomas have mutations that can be targeted by specific drugs, such as BRAF inhibitors. This is an area of ongoing research, with clinical trials being conducted.

Immunotherapy

  • Immune Checkpoint Inhibitors: Experimental use in craniopharyngiomas, focusing on harnessing the body's immune system to fight tumor cells. This approach is still largely in the research phase.

Modernity of Treatments

  • #Surgical Techniques: Advanced significantly with the development of endoscopic and minimally invasive approaches in the 2000s.
  • Radiation Therapy: Proton beam therapy has been a recent advancement, becoming more widely available over the past two decades.
  • Targeted and Immunotherapy: Still largely experimental, with ongoing clinical trials as of 2023.

Craniopharyngioma remains a challenging condition due to its complex location and potential impact on various physiological functions. While surgical and radiation therapies form the cornerstone of treatment, ongoing research into more targeted and less invasive treatments holds promise for the future.