Cronkhite–Canada syndrome

From WikiMD.org
Jump to navigation Jump to search

Cronkhite–Canada syndrome (pronunciation: krɒnˈkaɪt kəˈnædə sɪnˈdroʊm) is a rare, nonhereditary gastrointestinal condition characterized by the presence of multiple polyps in the stomach, small intestine, and large intestine.

Etymology

The syndrome is named after the American physicians Leonard W. Cronkhite Jr. and Wilma Canada who first described the condition in 1955.

Symptoms

The symptoms of Cronkhite–Canada syndrome include diarrhea, weight loss, abdominal pain, anemia, and changes in the skin, hair, and nails.

Diagnosis

Diagnosis of Cronkhite–Canada syndrome is typically made through a combination of endoscopy, biopsy, and imaging studies.

Treatment

Treatment for Cronkhite–Canada syndrome often involves nutritional support, corticosteroids, and in some cases, surgery to remove large polyps.

Prognosis

The prognosis for individuals with Cronkhite–Canada syndrome varies, but the condition is often associated with a high mortality rate due to complications such as malnutrition, sepsis, and cancer.

See also

External links

Esculaap.svg

This WikiMD article is a stub. You can help make it a full article.


Languages: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski