| LTN | lateral telangiectatic nevus |
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| BA | Bacillary angiomatosis |
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| 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) |
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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) |
| 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) |
| telangiectatic | Relating to or marked by telangiectasia. (05 Mar 2000) |
| telangiectatic angioma | <tumour> Angioma composed of dilated vessels. Angioma venosum racemosum, tortuous swelling caused by varicosities of superficial veins. Venous angioma, vascular anomaly composed of anomalous veins. (05 Mar 2000) |
| telangiectatic cancer | A cancer with numerous dilated capillaries and "lakes" of blood within relatively large endothelium-lined channels. (05 Mar 2000) |
| telangiectatic fibroma | <tumour> A benign neoplasm of fibrous tissue in which there are numerous, small and large, frequently dilated, vascular channels. Synonym: angiofibroma. (05 Mar 2000) |
| telangiectatic glioma | <tumour> Glioma telangiectodes, a glioma in which the stroma has numerous, conspicuous, frequently dilated small blood vessels and capillaries, as well as large, endothelium-rimmed lakes of blood. (05 Mar 2000) |
| telangiectatic lipoma | A benign neoplasm composed of a mixture of adipose tissue and blood vessels. (12 Dec 1998) |
| telangiectatic osteogenic sarcoma | <tumour> A lytic cystic variant of osteogenic sarcoma composed of aneurysmal blood-filled spaces lined by sarcoma cells producing osteoid. (05 Mar 2000) |
| telangiectatic wart | A discrete, pink to red telangiectasia having a tendency to undergo secondary epithelial changes, including acanthosis and hyperkeratosis. An underlying vascular abnormality is present in many cases. The term angiokeratoma is applied to a number of quite distinct conditions which share a common clinical presentation with asymptomatic hyperkeratotic vascular skin lesions and a histological combination of superficial dermal vascular ectasia. (12 Dec 1998) |
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