Carcinoid syndrome causes
Carcinoid syndrome Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Carcinoid syndrome causes On the Web |
American Roentgen Ray Society Images of Carcinoid syndrome causes |
Risk calculators and risk factors for Carcinoid syndrome causes |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Parminder Dhingra, M.D. [2]
Overview
Majority of the cases of gastrointestinal carcinoid are sporadic, however gastrointestinal carcinoid is associated with mutations in MEN1 and NF1 genes.
Causes
Common causes of carcinoid syndrome include:
- Genetic disorders
- Multiple endocrine neoplasia type 1
- Neurofibromatosis type 1.[1]
- Carcinoids associated with multiple endocrine neoplasia type 1 appear to be of foregut origin.
- Carcinoids in patients with neurofibromatosis type 1 appear to arise primarily in the periampullary region.
- In sporadic gastrointestinal carcinoids, numerous chromosomal imbalances have been found by comparative genome hybridization analysis.
- Gains involving chromosomes 5, 14, 17 (especially 17q), and 19 and losses involving chromosomes 11 (especially 11q) and 18 appear to be the most common.
References
- ↑ Molecular genetics. National Cancer Institute. http://www.cancer.gov/types/gi-carcinoid-tumors/hp/gi-carcinoid-treatment-pdq