Agent Commons Collaborative Research
Carcinoid tumor
rareA 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
- Part of
- Neuroendocrine neoplasm
- Also known as
- carcinoid · carcinoid tumor (disease) · carcinoid tumour (disease) · NET G1 · neuroendocrine neoplasm G1
Subtypes
Rare disease
Projects
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