| UGIS | Upper Gastro-Intestinal Series |
|---|---|
| VIP | Vasoactive Intestinal (Poly)Peptide |
| AII | acute intestinal infection; second meiotic anaphase |
| CIA | chemiluminescent immunoassay; chymotrypsin inhibitor activity; colony-inhibiting activity; congenita... |
| CIIP | chronic idiopathic intestinal pseudo-obstruction |
| VIP | Vaso-active intestinal polypeptide |
|---|---|
| VIC | Vasoactive Intestinal Contractor |
| VIP-LI | Vasoactive intestinal polypeptide-like immunoreactivity |
| I | intestinal |
| familial intestinal polyposis | Begins usually in late childhood; polyps increase in numbers, causing symptoms of chronic colitis, and carcinoma of the colon almost invariably develops in untreated cases; autosomal dominant inheritance. In the Gardner syndrome there are extracolonic changes (desmoid tumours, etc.). Synonym: polyposis coli. Hamartomatous polyposis of the small or large intestine, Peutz-Jeghers syndrome with melanin spots on the lips, less common, miscellaneous, rare, and doubtful occurrences. Synonym: familial intestinal polyposis. (05 Mar 2000) |
|---|---|
| lieno-intestinal | <anatomy> Of or pertaining to the spleen and intestine; as, the lieno-intestinal vein of the frog. Origin: l. Lien the spleen + E. Intestinal. Source: Websters Dictionary (01 Mar 1998) |
| lipophagic intestinal granulomatosis | An obsolete term for Whipple's disease. (05 Mar 2000) |
| lymphangiectasis, intestinal | Dilatation of the intestinal lymphatic system, particularly in the lacteals in the intestinal villi, characterised by protein-losing enteropathy, steatorrhoea, and lymphopenia. It may be congenital, due to abnormality of the lymphatic system (as in milroy's disease) or acquired, due to involvement of the major intestinal lymphatic ducts by inflammatory processes or neoplasm, or to increased lymphatic pressure, as in valvular heart disease and constrictive pericarditis. (12 Dec 1998) |