| small bowel lymphoma | <radiology> Patterns:, infiltrative dilatation, nodular multiple filling defects, polypoid may cause intussiception from leading point associated with Burkitt lymphoma, endoexoenteric fistulae (12 Dec 1998) |
|---|---|
| small bowel nodules | <radiology> Lymphoid hyperplasia, lymphoma, metastasis (12 Dec 1998) |
| small bowel obstruction | <radiology> Fibrous adhesions (75%), secondary to previous peritonitis or surgery, hernia, external, internal, neoplasm, inflammatory disease See also: adynamic ileus simulating mechanical obstruction, large bowel (colon) obstruction (12 Dec 1998) |
| small bowel series | Radiographic examination of the small intestine following the oral administration of contrast medium, usually barium sulfate. Compare: small bowel enema. (05 Mar 2000) |
| diffuse small bowel disease | <radiology> SWELL GAMES, S sprue, dilatation, dilution, moulage, reversal of jejunal and ileal patterns, W Whipple disease, coarse nodular and irregular mucosa, E oedema, L lymphangiectasis, nodular, thickened folds, L lymphoma, nodular, thickened folds, G giardiasis, oedema and spasm of proximal small bowel, A amyloid, symmetric fold thickening, M mastocytosis, look for sclerotic bones, E eosinophilic gastroenteritis, thickened, nodular folds and spasm, S stasis syndromes see: small bowel disease (12 Dec 1998) |
| inflammatory bowel disease | <disease> A general term that encompasses several disease processes, most commonly, ulcerative colitis and Crohn's disease. (27 Sep 1997) |
| inflammatory bowel diseases | Chronic, non-specific disorders of unknown aetiology. Includes crohn disease and ulcerative colitis. Extracolonic manifestations are often associated with inflammatory bowel disease (ibd) and involve the liver, joints and skin. (12 Dec 1998) |
| intramural bowel gas | <radiology> Pneumatosis cystoides intestinalis, necrotizing enterocolitis (NEC) - infants, mesenteric vascular thrombosis, necrosis due to strangulated obstruction, toxic ulcerative colitis, ulceration proximal to obstructing carcinoma, post-surgical changes (12 Dec 1998) |
| ischaemic bowel disease | <surgery> A disorder which results from the inadequate flow of oxygenated blood to the intestines. Symptoms include crampy abdominal pain after eating. More common in those with a history of atherosclerosis and-or diabetes. (15 Oct 1997) |
| thick small bowel folds | <radiology> Haemorrhage, oedema, ischemia, sprue, malabsorption, hypoproteinaemia, Whipple disease, amyloidosis, Henoch-Schonlein syndrome, abetalipoproteinaemia, Crohn disease (12 Dec 1998) |
| tubular small bowel | <radiology> (toothpaste small bowel) globally featureless small bowel: mucosal folds effaced, graft-vs.-host disease (GvH), Mycobacterium avium complex (MAC) (in AIDS), ischemia, Crohn disease, radiation, Strongyloides, milk enteropathy, sprue, corrosive enteritis, lymphoma, amyloidosis, mastocytosis, FUDR toxicity (12 Dec 1998) |
| localised small bowel disease | <radiology> Crohn's, tumour (including lymphoma), bleed/oedema (12 Dec 1998) |
| Aarskog-Scott syndrome | A syndrome of ocular hypertelorism, anteverted nostrils, broad upper lip, saddle-bag scrotum, and laxity of ligaments resulting in genu recurvatum, flat feet, and hyperextensible fingers; X-linked and autosomal dominant forms. Synonym: Aarskog-Scott syndrome. (05 Mar 2000) |
| Aarskog syndrome | <syndrome> Grier et al. (1983) reported father and 2 sons with typical Aarskog syndrome, including short stature, hypertelorism, and shawl scrotum. They tabulated the findings in 82 previous cases. X-linked recessive inheritance has been repeatedly suggested. The family reported by Welch (1974) had affected males in 3 consecutive generations. Thus, there is either genetic heterogeneity or this is an autosomal dominant with strong sex-influence and possibly ascertainment bias resulting from use of the shawl scrotum as a main criterion. Stretchable skin was present in the cases of Grier et al. (1983). Teebi et al. (1993) reported the case of an affected mother and 4 sons (including a pair of monozygotic twins) by 2 different husbands. They suggested that the manifestations were as severe in the mother as in the sons and that this suggested autosomal dominant inheritance. Actually, the mother seemed less severely affected, compatible with X-linked inheritance. Clinical signs: Mild to moderate short stature,normocephaly, Widow's peak hair, maxillary hypoplasia, broad nasal bridge, anteverted nostrils, long philtrum, broad upper lip, curved linear dimple below the lower lip, hypertelorism, ptosis, down-slanted palpebral fissures, ophthalmoplegia, strabismus, hyperopic astigmatism, large cornea, floppy ears, lop-ears,cleft lip/palate, shawl scrotum, saddle-bag scrotum, cryptorchidism, brachydactyly, digital contractures, clinodactyly, mild syndactyly, transverse palmar crease, lymphoedema of the feet, ligamentous laxity, osteochondritis dissecans, proximal finger joint hyperextensibility, flexed distal finger joints, genu recurvatum, flat feet, stretchable skin, cervical spine hypermobility, odontoid anomaly, macrocytic anaemia, hemochromatosis, hepatomegaly, portal cirrhosis, imperforate anus, rectoperineal fistula, interstitial pulmonary disease, sternal deformity. Inheritance: Sex-influenced autosomal dominant form, also X-linked form. (05 Aug 1998) |
| abdominal muscle deficiency syndrome | <syndrome> Congenital absence (partial or complete) of abdominal muscles, in which the outline of the intestines is visible through the protruding abdominal wall; in males, genitourinary anomalies (urinary tract dilation and cryptorchidism) are also found; genetics unclear. (05 Mar 2000) |