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Causes of Carcinoid Syndrome Diarrhea
Carcinoid syndrome diarrhea is caused by neuroendocrine tumors, commonly known as carcinoid tumors. These rare tumors usually originate in the gastrointestinal tract or lungs and secretes hormones and amines like serotonin. Serotonin causes symptoms like diarrhea when it reaches the intestines in high amounts from the tumors. The tumors are mostly non-cancerous but can spread to other organs if not treated on time. Around 10-15% of neuroendocrine tumors lead to carcinoid syndrome as they release high levels of serotonin and other substances in the bloodstream.
Symptoms of Carcinoid Syndrome Diarrhea
Some key symptoms of carcinoid syndrome diarrhea include:
- Watery Carcinoid Syndrome Diarrhea Treatment is occurring several times a day, which may be accompanied by abdominal cramping. Stools can range from loose to watery.
- Flushing of the face and upper body. It presents as redness or blotchiness of the skin and may be triggered by stress, alcohol, hot foods etc.
- Shortness of breath or wheezing. Excess serotonin in the body can cause bronchoconstriction.
- Weight loss due to malabsorbtion of nutrients from frequent diarrhea.
- Fatigue and weakness due to malnutrition.
- Valvular heart disease caused by accumulation of serotonin in the heart valves over time.
The symptoms may vary between patients and the severity depends on the size and location of tumors as well as the amounts of hormones secreted. Carcinoid syndrome diarrhea is usually chronic and persists if the underlying cause is not treated.
Diagnosis of Carcinoid Syndrome Diarrhea
To diagnose carcinoid syndrome diarrhea, doctors evaluate the symptoms and perform the following tests:
- Blood tests to check levels of serotonin and its breakdown products like 5-HIAA. Elevated levels indicate a carcinoid tumor.
- Imaging tests like CT scans or MRIs to locate the primary tumor as well as metastases. Octreotide scans using radiolabeled somatostatin analogs are highly accurate.
- Endoscopy with biopsies of the gastrointestinal tract if tumors are suspected in these regions. Bronchoscopy for lung lesions.
- Tissue sampling and histopathological examination during surgery is required for confirmation.
- Genetic testing in some cases may help determine if it is non-hereditary carcinoid or part of genetic conditions like multiple endocrine neoplasia type 1 (MEN1).
The goal is to pinpoint the exact location and size of tumors triggering carcinoid syndrome diarrhea to plan the most suitable treatment approach.
Treatment Options for Carcinoid Syndrome Diarrhea
Several treatment options are available depending on tumor stage, severity of symptoms, age, and overall health of the patient:
- Somatostatin analogs like octreotide are considered first-line treatment and are very effective against carcinoid syndrome diarrhea in around 70-90% cases. They reduce serotonin production and release from tumors. Administered via injections or implants under the skin.
- Hepatic arterial embolization aims to cut blood supply to liver tumors which are common sites of metastases responsible for serotonin overflow. Works well for controlling symptoms in around 60-80% cases.
- Radiotherapy using gamma knife, proton beam therapy or stereotactic body radiation therapy to treat small, localized tumors that cannot be surgically removed. Provides lasting symptom relief.
- Surgery to remove primary tumors as well as metastasized ones if technically feasible. Complete surgical resection achieves remission in around 80% cases.
- Chemotherapy for advanced, metastasized tumors that have progressed beyond other treatment options. Options include streptozocin, fluorouracil, doxorubicin, dacarbazine etc.
- Biotherapy using lanreotide autogel is an option for patients not tolerating octreotide implants.
- Antidiarrheal medications like loperamide, cholestyramine or colestipol to manage symptoms alongside primary treatment.
- Managing stress and avoiding triggers that cause flushing also helps mitigate symptoms in some patients.
The goal of treatment is achieving remission along with keeping symptoms like diarrhea under control to improve quality of life. A multidisciplinary team approach including oncologists, surgeons and other specialists provides best outcomes. Long term surveillance is required due to possibility of recurrence or regrowth of tumors.
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About Author:
Ravina Pandya, Content Writer, has a strong foothold in the market research industry. She specializes in writing well-researched articles from different industries, including food and beverages, information and technology, healthcare, chemical and materials, etc. (https://www.linkedin.com/in/ravina-pandya-1a3984191)


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