Carcinoid Syndrome - Symptom, Treatment and cause of Carcinoid Syndrome

Carcinoid Syndrome Description

A cancer that starts in argentaffin cells inside the small intestine, stomach or lung.

Carcinoid Syndrome Cause

Argentaffin cells are responsible for producing a number of essential hormones (e.g. serotonin) for the functioning of the gut and body in general. When these cells become cancerous, they produce excessive amounts of these hormones, which causes unusual symptoms.

Carcinoid Syndrome Symptom

May develop very rapidly, and patients can become severely ill in a few days. Symptoms include hot flushes of the face, swelling of the head and neck, diarrhea and stomach cramps, asthma and bleeding into the skin.

Investigation

Blood or urine tests can be carried out to identify the high levels of serotonin and other hormones.

Carcinoid Syndrome Treatment

Prednisone (a steroid) is used in the emergency treatment of the disease, and other medications are given to control the other symptoms. Drugs such as interferon can sometimes be used to destroy the cancer cells.

Complications

The site of the cancer is often very difficult to find, as it is usually very small and slow growing. It also tends to spread at an early stage to other areas, so even if the original is removed, the syndrome may continue due to the production of hormones in high levels by newly formed and very small cancers in multiple sites.

Prognosis of Carcinoid Syndrome

Because of its slow growth rate, it may take 10 or 15 years for the disease to progress from the stage of being a nuisance that requires constant medication, to being life-threatening.

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