| DCS | decompression sickness; dense canalicular system; diffuse cortical sclerosis; dorsal column stimulat... |
|---|---|
| DFE | diffuse fasciitis with eosinophilia; distal femoral epiphysis |
| DGN | diffuse glomerulonephritis |
| DGPG | diffuse proliferative glomerulonephritis |
| DHL | diffuse histiocytic lymphoma |
| 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 small cleaved cell lymphoma | <tumour> A diffuse poorly differentiated lymphocytic lymphoma; follicular centre cell lymphoma that lacks a follicular pattern; malignancy is of intermediate grade. (05 Mar 2000) |
| 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) |
| 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) |
| lymphoma, diffuse | Malignant lymphoma in which neoplastic cells diffusely infiltrate the entire lymph node without any definite organised pattern. Patients whose lymphomas present a diffuse pattern generally have a more unfavorable survival outlook than those presenting with a follicular or nodular pattern. (12 Dec 1998) |
| lymphoma, large-cell, diffuse | Malignant lymphoma composed of large cells which may be both cleaved and noncleaved. The pattern is predominantly diffuse. most of these lymphomas represent the malignant counterpart of B-lymphocytes at midstage in the process of differentiation. (12 Dec 1998) |
| lymphoma, mixed-cell, diffuse | A heterogeneous group of intermediate-grade lymphomas of mixed cellular composition. Although they have not been extensively studied, it appears that they are predominantly B-cell diseases. (12 Dec 1998) |
| lymphoma, small cleaved-cell, diffuse | An intermediate-grade malignant lymphoma in which the neoplastic cells (B-lymphocytes) exhibit variability in size, configuration, and degree of differentiation. The cells have distinctive nuclei, irregular in shape, with marked indentations and angularity. (12 Dec 1998) |
| reflux, oesophageal | A condition wherein stomach contents regurgitate or back up (reflux) into the oesophagus (a long cylindrical tube that transports food from the mouth to the stomach). The food in the stomach is partially digested by stomach acid and enzymes. Normally, the partially digested acid content in the stomach is delivered by the stomach muscle into the small intestine for further digestion. In oesophageal reflux, stomach acid content refluxes backwards up into the oesophagus, occasionally reaching the breathing passages, causing inflammation and damage to the oesophagus, as well as to the lung and larynx (the voice box). The overall process is medically termed gastroesophageal reflux disease (gerd). 10% of patients with gerd develop a barrett's oesophagus which can increase the risk of cancer of the oesophagus. (12 Dec 1998) |
| cervical oesophageal web | <radiology> Post-cricoid web, M=F, 5% of UGI patients, anterior (antero-lateral), with or without dysphagia, Treatment: endoscopic disruption (lysis) see: oesophageal webs and rings (12 Dec 1998) |
| sliding oesophageal hiatal hernia | Displacement of the cardioesophageal junction and the stomach through the oesophageal hiatus. (05 Mar 2000) |