Usually, these tumors grow slowly at the base of the skull and the lower part of the spine. They
are mostly seen among individuals at the age group of 50-60. Even though they are
non-cancerous, they may cause excess pressure on the nearby neural tissues. They derive
from the remnants of the embryonic notochord. They are incessant and may recur even after a
course of treatment. Main treatment option for chordomas is the surgery. With the surgery, the
tumor can be removed partially, or completely. Chordomas are very rare, which contribute only
0.2% of all primary brain tumors hh hfd b vfhndc.
They derive from the embryogenic remnants in the core of Pituitary Gland. These benign tumors
may even attack the surrounding structures also. They will have both cystic as well as solid
components. It is difficult to discover craniopharyngiomas in an individual unless it press or
invade the vital structures that surround the hypothalamus or the optic nerve region.
The most common symptoms seen in children affected by Craniopharyngioma are:
- Lack of growth
- Precocious puberty
- Vomiting etc.
Visual field defect is the most common symptom seen among adults with Craniopharyngioma.
Overall incidents of Craniopharyngioma are calculated as 0.18 per 100,000 people per years.
The condition may not vary according to gender or race. 4.1% of tumors that affect the children
The best method used for diagnosing Craniopharyngiomas is an MRI with contrast.
The most preferred treatment is microsurgical excision and a Transcranial route through
craniotomy. Procedures such as Expanded Endonasal Approach and Endoscopic removal of
tumors are also chosen in certain cases. The surgery will have 86-99% of success rates. The
condition may recur even after the complete removal. Radiation and or Intra tumoral Bleomycin
are used for recurrence or residual tumor.