| diffuse mesangial proliferation | <nephrology, pathology> Inflammation of the kidney glomerulus (blood filtering portion of the kidney) due to the abnormal deposition of IgM antibody in the mesangium layer of the glomerular capillary. A form of glomerulonephritis that appears to be caused by an abnormal immune response. This disorder generally manifests as nephrotic syndrome. Symptoms include swelling, dark urine, weight gain, hypertension, anorexia and bloody urine. Acronym: MPGN (05 Jan 1998) |
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| diffuse nontoxic goitre | A common cause of hyperthyroidism thought to be caused by an underlying autoimmune mechanism. (27 Sep 1997) |
| diffuse obstructive emphysema | The major component of chronic obstructive lung disease. (05 Mar 2000) |
| diffuse oesophageal spasm | A disorder characterised by episodic contractions of the oesophagus. The oesophageal spasms fail to effectively propel food to the stomach. Symptoms may be confused with angina. Common symptoms include chest pains, epigastric pain, heartburn, pain on swallowing and difficulty swallowing. Treatment includes the use of sublingual nitroglycerin and calcium channel blockers. (27 Sep 1997) |
| diffuse osteosclerosis | <radiology> Mnemonic: 3M PROFS, renal osteodystrophy, metastasis, mastocytosis, myelofibrosis, sickle cell disease, osteopetrosis (Albers-Schoenberg disease), pyknodysostosis, fluorosis (12 Dec 1998) |
| diffuse panbronchiolitis | Idiopathic inflammation and obstruction of bronchioles, eventually accompanied by bronchiectasis; cases reported almost entirely from Japan. Synonym: diffuse panbronchiolitis. (05 Mar 2000) |
| diffuse peritonitis | Peritonitis throughout the peritoneal cavity. Synonym: diffuse peritonitis. (05 Mar 2000) |
| diffuse phlegmon | A diffuse inflammation of the subcutaneous tissues accompanied by constitutional symptoms of sepsis. (05 Mar 2000) |
| diffuse pulmonary haemorrhage | <radiology> Thrombocytopenia, coagulopathy, idiopathic pulmonary haemosiderosis, Goodpasture syndrome, systemic lupus erythematosus, Wegeners granulomatosis, polyarteritis nodosa, Henoch-Schonlein purpura, Behcet disease, D-penicillamine, lymphangiography (12 Dec 1998) |
| 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) |
| diffuse waxy spleen | A condition of amyloid degeneration of the spleen, affecting chiefly the extrasinusoidal tissue spaces of the pulp. Synonym: lardaceous spleen (05 Mar 2000) |
| oesophageal spasm, diffuse | A motor disorder of the oesophagus characterised by chest pain and dysphagia. Pathogenesis is unclear. Strong, nonpropulsive contractions of the oesophagus evoked by deglutition occur, especially in the elderly. (12 Dec 1998) |
| keratoderma, palmoplantar, diffuse | An autosomal dominant disorder characterised by a widely distributed, well-demarcated hyperkeratosis of the palms and soles. There is more than one genotypically distinct form, each of which is clinically similar but histologically distinguishable. Diffuse palmoplantar keratoderma is distinct from palmoplantar keratoderma (keratoderma, palmoplantar), as the former exhibits autosomal dominant inheritance and hyperhidrosis is frequently present. (12 Dec 1998) |
| leishmaniasis, diffuse cutaneous | A form of leishmaniasis, cutaneous caused by leishmania aethiopica in ethiopia and kenya, l. Pifanoi in venezuela, l. Braziliensis in south america, and l. Mexicana in central america. This disease is characterised by massive dissemination of skin lesions without visceral involvement. (12 Dec 1998) |
| leukodystrophy with diffuse Rosenthal fibre formation | A metabolic disorder whose onset can be in infancy, adolescence, or adulthood; characterised pathologically by widespread cerebral demyelination with astrocyte and primitive oligodendroglial cell proliferation; refractile Rosenthal fibres result from the degeneration of these proliferating cells; aetiology unknown, but possibly due to a metabolic defect of astrocytes; sex-linked recessive disorder. (05 Mar 2000) |