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Carcinoid syndrome

Last updated: March 18, 2025

Summarytoggle arrow icon

Carcinoid syndrome is a paraneoplastic condition caused by intermittent secretion of serotonin and other vasoactive substances (e.g., kallikrein, histamine) by neuroendocrine neoplasms (NENs). It is primarily associated with metastatic well-differentiated NENs, i.e., neuroendocrine tumors (NETs), in the gastrointestinal tract. Symptoms include episodic cutaneous flushing, diarrhea, abdominal pain, and wheezing. In advanced cases, manifestations can include pellagra, mesenteric fibrosis, and cardiac valvular fibrosis (particularly affecting the right heart). Elevated urinary 5-hydroxyindoleacetic acid (5-HIAA) levels confirm the diagnosis. Imaging (e.g., CT, MRI, PET/CT) is used for locating tumors and staging. Somatostatin analogues (e.g., octreotide) are first-line treatments. Carcinoid crisis is a potentially life-threatening complication that is typically triggered by general anesthesia and/or perioperative manipulation of the NEN due to an efflux of vasoactive substances; prevention involves perioperative somatostatin analogue infusion.

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Epidemiologytoggle arrow icon

  • Incidence: 2.7 per 1,000,000 population per year [1]
  • =
  • Highest in African-American individuals

Epidemiological data refers to the US, unless otherwise specified.

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Pathophysiologytoggle arrow icon

Carcinoid syndrome is a paraneoplastic condition caused by excess production, storage, and systemic circulation of multiple different hormones synthesized by certain metabolically active NENs. [1][2][3]

Serotonin is degraded via first-pass metabolism in the liver and by monoamine oxidases in the lungs.

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Clinical featurestoggle arrow icon

Carcinoid syndrome is caused by intermittent secretion of serotonin and other vasoactive substances by NENs. [1][3]

Consider carcinoid syndrome and workup for a NEN in patients presenting with secretory diarrhea, episodic flushing, wheezing, and right-sided cardiac valvular abnormalities.

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Diagnosistoggle arrow icon

Biochemical testing [1]

The following studies can be used to diagnose carcinoid syndrome and/or monitor disease progression in consultation with a specialist (e.g., endocrinologist).

Imaging [1][7]

Imaging studies are used to locate primary and metastatic NENs.

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Differential diagnosestoggle arrow icon

Endocrine differential diagnoses of carcinoid syndrome
Blood glucose Diarrhea Associated genetic syndromes Other findings
Carcinoid syndrome [3][9]
  • Normal
  • Yes (watery)
Zollinger-Ellison syndrome [10]
  • Normal
VIPoma [11]
Pheochromocytoma [4][9]
  • Slightly ↑
  • No
Medullary thyroid carcinoma [12]
  • Normal
Mastocytosis [13]
  • Normal
  • None
Hyperthyroidism [4]
  • Sometimes (due to intestinal hypermotility)
  • None

The differential diagnoses listed here are not exhaustive.

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Treatmenttoggle arrow icon

Treatment of carcinoid syndrome should be guided by appropriate specialists (e.g., oncology, gastroenterology) and includes both symptomatic management and treatment of the causative neuroendocrine neoplasm.

Pharmacological treatment [1][7]

Surgery and interventional treatment [1][7]

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Complicationstoggle arrow icon

Carcinoid crisis [1][7]

Long-term complications [1]

We list the most important complications. The selection is not exhaustive.

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