| GNBP | Gram Negative(-) Bacillary Pneumonias |
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| Bac, bac | Bacillus, bacillary |
| BE | bacillary emulsion; bacterial endocarditis; barium enema; Barrett's esophagus; base excess; below-el... |
| BWD | bacillary white diarrhea |
| GNBM | gram-negative bacillary meningitis |
| BA | Bacillary angiomatosis |
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| angiomatosis, bacillary | An infectious bacterial disease characterised by cutaneous vascular lesions. It is caused by bartonella henselae and is seen in aids patients and other immunocompromised hosts. (12 Dec 1998) |
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| bacillary | Shaped like a rod; consisting of rods or rodlike elements. (05 Mar 2000) |
| bacillary dysentery | Infection with Shigella dysenteriae, S. Flexneri, or other organisms. Synonym: Japanese dysentery. (05 Mar 2000) |
| bacillary haemoglobinuria | An acute toxaemic disease of cattle caused by the bacterium Clostridium haemolyticum and characterised by severe depression, fever, abdominal pain, dyspnea, dysentery, haemoglobinuria, and rapid death; also occurs in sheep and, rarely, in dogs. (05 Mar 2000) |
| bacillary layer | The layer of the retina next to the pigment layer and containing the visual receptors. See: retina, granular layers of retina, neuroepithelial layer of retina. Synonym: bacillary layer. (05 Mar 2000) |
| chronic bacillary diarrhoea | Prolonged diarrhoea occurring in association with bacterial infection, usually occurring in patients with gastrointestinal stasis, allowing bacterial proliferation in the intestine with secondary malabsorption. Occurs in blind-loop syndrome after intestinal surgery, following vagotomy, and occasionally in scleroderma or diabetes. (05 Mar 2000) |
| dysentery, bacillary | An infectious disease caused by bacteria of the genus shigella. This condition is characterised by intestinal pain and diarrhoea. (12 Dec 1998) |
| angiomatosis | A condition characterised by multiple angiomas. Bacillary angiomatosis, an infection of immunocompromised patients by a newly recognised Rickettsial species Rochalimaea henselae, characterised by fever and granulomatous cutaneous nodules, and peliosis hepatis in some cases. Skin biopsy shows vascular proliferation and infiltration of vessel walls by neutrophils and clumps of organisms seen with Warthin-Starry silver staining. (05 Mar 2000) |
| cephalotrigeminal angiomatosis | <syndrome> A congenital syndrome consisting of nevus flammeus of the face, haemangiomas of the leptomeninges and choroid, and late glaucoma. It is often associated with intracranial calcification, mental retardation, contralateral hemiplegia, and epilepsy. (12 Dec 1998) |
| cerebroretinal angiomatosis | <radiology> Retinocerebellar angiomatosis, phakomatosis, autosomal dominant (variable penetrance), haemangioblastoma: most frequent cause of death, cerebellar (most common), also medullary and spinal, retinal angiomatosis (45%), renal cell carcinoma: 2nd most common cause of death, pheochromocytoma (17%), cortical renal cysts (75%), cysts in virtually any organ, renal/liver haemangioma/adenoma, pancreatic cystic neoplasms, isleT-cell tumours, paraganglioma (12 Dec 1998) |
| congenital dysplastic angiomatosis | Autosomal dominant angiomatosis in which there is dysplasia of the underlying tissues, sometimes with overgrowth of bone (Klippel-Trenaunay-Weber syndrome), or encephalotrigeminal angiomatosis (Sturge-Weber syndrome) in which there is an angioma in the distribution of one or more branches of the trigeminal nerve, with vascular anomalies and calcification of the cerebral cortex. (05 Mar 2000) |
| cutaneomeningospinal angiomatosis | <syndrome> Cutaneous angiomas, usually in a dermatomal distribution on the trunk, associated with vascular abnormality of the spinal cord and resulting neurologic symptoms. Synonym: cutaneomeningospinal angiomatosis. (05 Mar 2000) |
| oculoencephalic angiomatosis | An incomplete autosomal dominant form of Sturge-Weber syndrome, consisting of angiomas of the choroid and meninges only. Telangiectatic angiomatosis, disseminated capillary and venous vascular malformations of the cerebral hemispheres and leptomeninges, occurring in Sturge-Weber syndrome. (05 Mar 2000) |
| encephalotrigeminal angiomatosis | <syndrome> A congenital syndrome consisting of nevus flammeus of the face, haemangiomas of the leptomeninges and choroid, and late glaucoma. It is often associated with intracranial calcification, mental retardation, contralateral hemiplegia, and epilepsy. (12 Dec 1998) |
| bacillary angiomatosis |
a condition seen in immunocompromised patients, caused by Bartonella henselae and B. quintana; characteristics range from raised erythematous angiomatous skin lesions to more widespread disease including hepatitis, osteomyelitis, or obstruction of the lungs.
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