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(D44.4) Neoplasm of uncertain or unknown behaviour: craniopharyngeal duct
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680 796 in individuals diagnosis neoplasm of uncertain or unknown behaviour: craniopharyngeal duct confirmed
13 840 deaths with diagnosis neoplasm of uncertain or unknown behaviour: craniopharyngeal duct
2% mortality rate associated with the disease neoplasm of uncertain or unknown behaviour: craniopharyngeal duct
Diagnosis neoplasm of uncertain or unknown behaviour: craniopharyngeal duct is diagnosed Women are 28.99% more likely than Men
241 718
Men receive the diagnosis neoplasm of uncertain or unknown behaviour: craniopharyngeal duct
6 552 (2.7 %)Died from this diagnosis.
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Women receive the diagnosis neoplasm of uncertain or unknown behaviour: craniopharyngeal duct
7 288 (1.7 %)Died from this diagnosis.
Risk Group for the Disease neoplasm of uncertain or unknown behaviour: craniopharyngeal duct - Men and Women aged 60-64
In Men diagnosis is most often set at age 0-94
Less common in men the disease occurs at Age 95+in in women, the disease manifests at any age
In Women diagnosis is most often set at age 0-95+
Disease Features neoplasm of uncertain or unknown behaviour: craniopharyngeal duct
Absence or low individual and public risk
Neoplasm of uncertain or unknown behaviour: craniopharyngeal duct - what does this mean
Neoplasm of uncertain or unknown behaviour of the craniopharyngeal duct is a rare condition in which a tumor forms in the craniopharyngeal duct, which is the tube that connects the brain to the throat. the tumor can cause a variety of symptoms, including headaches, nausea, vomiting, and difficulty swallowing. treatment typically involves surgery to remove the tumor, followed by radiation and/or chemotherapy depending on the type of tumor.
What happens during the disease - neoplasm of uncertain or unknown behaviour: craniopharyngeal duct
Neoplasm of uncertain or unknown behaviour of the craniopharyngeal duct is a condition in which abnormal cells form in the craniopharyngeal duct, a tube connecting the brain and the throat. it is believed that the abnormal cell growth is caused by genetic mutations, environmental factors, or a combination of both. these mutations can cause the cells to grow and divide uncontrollably, forming a mass of abnormal tissue that can interfere with normal functioning of the craniopharyngeal duct.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Obtain a detailed medical history.
- Perform a physical examination.
- Order imaging tests such as X-ray, CT scan, or MRI.
- Perform a biopsy of the affected area.
- Order laboratory tests such as blood tests or genetic tests.
- Perform a lumbar puncture to obtain cerebrospinal fluid.
- Perform an endoscopy to view the inside of the cranial cavity.
- Perform a biopsy of the cranial nerve.
Treatment and Medical Assistance
Main goal of the treatment: To reduce the size of the neoplasm and reduce the risk of further complications.
- Imaging studies such as MRI or CT scans to assess the size and location of the neoplasm.
- Surgery to remove the tumor.
- Radiotherapy to shrink the tumor.
- Chemotherapy to reduce the tumor size.
- Endoscopic laser therapy to remove the tumor.
- Stereotactic radiosurgery to target the tumor.
- Follow-up imaging studies to monitor the tumor size.
12 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Neoplasm of uncertain or unknown behaviour: craniopharyngeal duct - Prevention
The best way to prevent neoplasm of uncertain or unknown behaviour: craniopharyngeal duct is to adopt a healthy lifestyle, including regular exercise, a balanced diet, and avoiding smoking and excessive alcohol consumption. regular check-ups with a doctor can also help to detect any changes in the body early on.