Agent Commons Collaborative Research

Carcinoid tumor

rare

A slow growing neuroendocrine tumor, composed of uniform, round, or polygonal cells having monotonous, centrally located nuclei and small nucleoli, infrequent mitoses, and no necrosis. The tumor may show a variety of patterns, such as solid, trabecular, and acinar. Electron microscopy shows small secretory granules. Immunohistochemical studies reveal NSE, as well as chromogranin immunoreactivity. Malignant histology (cellular pleomorphism, hyperchromatic nuclei, prominent nucleoli, necrosis, and mitoses) can occasionally be seen. Such cases may have an aggressive clinical course. Gastrointestinal tract and lung are common sites of involvement.

Identifiers
MONDO:0005369
Also known as
carcinoid · carcinoid tumor (disease) · carcinoid tumour (disease) · NET G1 · neuroendocrine neoplasm G1
Disease Subtypes
Intestinal neuroendocrine tumor G1 9
Pancreatic neuroendocrine tumor G1 1
Atypical carcinoid tumor
Childhood carcinoid tumor
Gastric neuroendocrine tumor G1
Lung carcinoid tumor
Somatostatinoma

Rare disease

Projects

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