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Carcinoid syndrome
 | This article needs more reliable medical references for verification or relies too heavily on primary sources. (March 2013) |  |
| Carcinoid syndrome | |
|---|---|
| Specialty | Endocrinology, oncology |
Carcinoid syndrome is a paraneoplastic syndrome comprising the signs and symptoms that occur secondary to neuroendocrine tumors (formerly known as carcinoid tumors).[1] The syndrome is caused by neuroendocrine tumors most often found in the gut releasing biologically active substances into the blood causing symptoms such as flushing and diarrhea, and less frequently, heart failure, vomiting and bronchoconstriction.[2][1]
- ^ a b Pandit, Sudha; Annamaraju, Pavan; Bhusal, Kamal (2022), "Carcinoid Syndrome", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 28846309, retrieved 2023-01-16
- ^ Rubin de Celis Ferrari AC; Glasberg, J.; Riechelmann, R. P. (2018). "Carcinoid syndrome: Update on the pathophysiology and treatment". Clinics (Sao Paulo, Brazil). 73 (suppl 1): e490s. doi:10.6061/clinics/2018/e490s. PMC 6096975. PMID 30133565.
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