WordNet
- a small tumor (benign or malignant) arising from the mucosa of the gastrointestinal tract; usually associated with excessive secretion of serotonin
English Journal
- Carcinoid tumors of the small-bowel: Evaluation with 64-section CT-enteroclysis.
- Soyer P, Dohan A, Eveno C, Dray X, Hamzi L, Hoeffel C, Kaci R, Boudiaf M.SourceDepartment of Body and Interventional Imaging, Hôpital Lariboisière - AP-HP, 2 rue Ambroise Paré, 75475 Paris Cedex 10, France; Université Paris-Diderot, Sorbonne-Paris Cité, 10 rue de Verdun, 75010 Paris, France; UMR INSERM 965, Hôpital Lariboisière, 2 rue Amboise Paré, 75010 Paris, France. Electronic address: philippe.soyer@lrb.aphp.fr.
- European journal of radiology.Eur J Radiol.2013 Jun;82(6):943-50. doi: 10.1016/j.ejrad.2013.02.013. Epub 2013 Mar 6.
- PURPOSE: To describe the imaging presentation of carcinoid tumors of the small-bowel at 64-section CT-enteroclysis and determine the sensitivity of this technique for tumor detection.PATIENTS AND METHODS: The 64-section CT-enteroclysis examinations of 22 patients with histopathologically proven smal
- PMID 23480964
- Causes of Death and Prognostic Factors in Multiple Endocrine Neoplasia Type 1 With Pancreatic Endocrine Tumor and Zollinger-Ellison Syndrome: Prospective Study of 106 Cases and Review of the Literature.
- Ito T, Igarashi H, Uehara H, Berna MJ, Jensen RT.SourceFrom the Department of Medicine and Bioregulatory Science (TI, HI), Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan; Digestive Diseases Branch (TI, HI, HU, MJB, RTJ), National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland; and Hôpital Kirchberg (MJB), Luxembourg, Luxembourg.
- Medicine.Medicine (Baltimore).2013 May 2. [Epub ahead of print]
- Multiple endocrine neoplasia type 1 (MEN1) is classically characterized by the development of functional or nonfunctional hyperplasia or tumors in endocrine tissues (parathyroid, pancreas, pituitary, adrenal). Because effective treatments have been developed for the hormone excess state, which was a
- PMID 23645327
- Ectopic Cushing's Syndrome Secondary to Pulmonary Carcinoid Tumor.
- Hashemzadeh S, Asvadi Kermani A, Ali-Asgharzadeh A, Halimi M, Soleimani M, Ladan A.SourceTuberculosis and Lung Diseases Research Center, Hematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
- The Annals of thoracic surgery.Ann Thorac Surg.2013 May;95(5):1797-9. doi: 10.1016/j.athoracsur.2012.09.039.
- Adrenocorticotropic hormone (ACTH) overproduction within the pituitary gland or ectopically leads to hypercortisolism. In this study a case of Cushing's syndrome caused by an ectopic ACTH-secreting carcinoid tumor in lung is discussed, as are the available diagnostic procedures. The patient was a 28
- PMID 23608267
Japanese Journal
- A-6. 神経芽細胞腫における生化学的検索
- 小野 磐夫,佐藤 辰男,吉永 馨
- 医化学シンポジウム 10(0), 27-31, 1971
- … Since 1961, the test has been routinely used in our clinic for screening of pheochromocytoma, neuroblastoma and argentaffinoma. …
- NAID 130003358507
- The ocular carcinoid syndrome components Malignant carcinoid:Argentaffinoma
- Monninger Robert H.G.
- 臨床眼科 23(3), 278-279, 1969-03
- NAID 40018587438
- Composite carcinoid tumor (argentaffinoma-adenocarcinoma) of the colon: report of two cases
- BATES H. R.
- Dis Colon Rectum 10, 467-470, 1967
- NAID 10005041155
Related Links
- argentaffinoma [ahr″jen-taf″ĭ-no´mah] a carcinoid tumor of the gastrointestinal tract formed from argentaffin cells, usually in the terminal ileum or appendix; such tumors elaborate a variety of catecholamines that produce the symptom ...
- argentaffinoma ar·gen·taf·fi·no·ma (är-jěn'tə-fə-nō'mə, är'jən-tāf'ə-) n. See carcinoid tumor.
Related Pictures
★リンクテーブル★
| リンク元 | 「嗜銀細胞腫」「carcinoid」 |
「嗜銀細胞腫」
- 英
- argentaffinoma, argentaffin cell tumor
- 同
- 銀親和細胞腫
- 関
- カルチノイド
「carcinoid」