Pulmonary carcinoid tumour: Difference between revisions
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Revision as of 18:47, 18 March 2025
Pulmonary Carcinoid Tumour
A Pulmonary Carcinoid Tumour is a rare type of cancer that develops in the lungs. It is a type of neuroendocrine tumour, which means it originates from cells in the body that produce hormones. Pulmonary carcinoid tumours are usually slow-growing and can take many years to develop.
Symptoms
The symptoms of a pulmonary carcinoid tumour can vary depending on its size and location. Common symptoms include:
- Cough that doesn't go away
- Chest pain
- Shortness of breath
- Wheezing
- Blood in the sputum (hemoptysis)
- Weight loss without trying
Causes
The exact cause of pulmonary carcinoid tumours is unknown. However, it is believed to be related to genetic mutations in the neuroendocrine cells of the lungs.
Diagnosis
Diagnosis of a pulmonary carcinoid tumour typically involves a combination of medical imaging tests, such as a CT scan or MRI, and a biopsy to examine the cells under a microscope.
Treatment
Treatment for a pulmonary carcinoid tumour depends on the size and location of the tumour, as well as the patient's overall health. Options may include surgery, radiation therapy, chemotherapy, or a combination of these treatments.
Prognosis
The prognosis for a pulmonary carcinoid tumour is generally good, especially if the tumour is detected early and can be completely removed with surgery. However, the prognosis can vary depending on the size and location of the tumour, as well as the patient's overall health.
