| filiform polyposis | <radiology> Benign, non-specific sequela of diffuse, severe mucosal inflammation, UC, Crohn's, XR: thin, straight filling defects, resembles stalks of polyps without heads (12 Dec 1998) |
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| filiform | Thread-like. (09 Oct 1997) |
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| filiform adnatum | Congenital adhesion of the upper and lower eyelid by bands of tissue. Synonym: filiform adnatum. Origin: ankylo-+ G. Blepharon, eyelid (05 Mar 2000) |
| filiform bougie | A very slender bougie usually used for gentle exploration of strictures or sinus tracts of small diameter where false passages can be encountered or created; the entering end can consist of either a straight or spiral tip, and the trailing end usually consists of a threaded cylinder into which the screw tip of a following bougie can be inserted. (05 Mar 2000) |
| filiform nucleus | A triangular group of large magnocellular neurons in the periventricular zone of the anterior half of the hypothalamus. The cells of the nucleus are similar to those of the supraoptic nucleus; the axons of about 20% of their number join in the formation of the supraopticohypophysial tract and are functionally associated with the posterior lobe of the hypophysis; they project fibres to the brainstem nuclei (dorsal motor nucleus and solitary nucleus) and to the intermediolateral cell column of the spinal cord at thoracic, lumbar, and spinal levels; similar descending autonomic fibres arise from the lateral and posterior hypothalamic nuclei. Synonym: nucleus paraventricularis, filiform nucleus, nucleus filiformis. (05 Mar 2000) |
| filiform papillae | Curved tapering cone shaped body on the tongue of rodents, of which the epithelial cell columns have been investigated in detail. (18 Nov 1997) |
| filiform pulse | A thready pulse. (05 Mar 2000) |
| filiform wart | A wart composed of a single or many greatly elongated papillae; appears more commonly on the face and neck. Synonym: filiform wart. (05 Mar 2000) |
| adenomatous polyposis coli | An autosomal dominant polyposis syndrome in which the colon contains few to thousands of adenomatous polyps, often occurring by age 15 to 25. (12 Dec 1998) |
| multiple 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) |
| polyposis | Presence of several polyps. Origin: polyp + G. -osis, condition (05 Mar 2000) |
| polyposis coli | Hereditary disorder (Mendelian dominant) characterised by the development of hundreds of adenomatous polyps in the large intestine, which show a tendency to progress to malignancy. The APC gene has also been implicated in a chromosome 5 gastric and pancreatic cancer. (18 Nov 1997) |
| polyposis syndromes | <radiology> Inher. Malig. Type familial polyposis coli dom and adenoma Gardner syndrome dom and Turcot syndrome rec CNS Peutz-Jeghers syndrome dom (+) hamartoma Cowden syndrome dom ? juvenile polyposis coli (?) - juvenile Cronkhite-Canada syndrome (12 Dec 1998) |
| juvenile polyposis coli | <radiology> Benign polyposis, inheritance uncertain, inflammatory or retention polyps: round, smooth, soft, mucin-filled, non-neoplastic, onset less than 10 yrs, polyps can prolapse through anus, associated with diarrhoea, protein loss see: polyposis syndromes, Cronkhite-Canada syndrome (12 Dec 1998) |
| familial adenomatous polyposis | <gastroenterology> Genetic disease with numerous precancerous polyps in the colon and rectum. Also called familial polyposis. (12 Dec 1998) |
| 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) |