Preferred Label : Carcinoid Tumor;
Obsolete resource : true;
NCIt synonyms : Carcinoid;
NCIt related terms : Enterochromaffin cell carcinoid;
NCIt definition : 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.;
Alternative definition : NCI-GLOSS: A slow-growing type of tumor usually found in the gastrointestinal system
(most often in the appendix), and sometimes in the lungs or other sites. Carcinoid
tumors may spread to the liver or other sites in the body, and they may secrete substances
such as serotonin or prostaglandins, causing carcinoid syndrome.;
NCIt note : See 'Neuroendocrine Tumor(C188218)';
Neoplastic status : Undetermined;
Concept status : Retired_Concept;
ICD-O code : 8240/3; 8241/3;
Codes from synonyms : CDR0000044233; 10007276;
Origin ID : C2915;
UMLS CUI : C0007095;
Automatic exact mappings (from CISMeF team)
Currated CISMeF NLP mapping
Disease may have findings
False automatic mappings
Semantic type(s)
UMLS correspondences (same concept)
disease_has_finding