| XTM | xanthoma tuberosum multiplex |
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| AMC | academic medical center; acetylmethyl carbinol; Animal Medical Center; antibody-mediated cytotoxicit... |
| AMC | Arthrogryposis Multiplex Congenita |
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| M-FISH | Multiplex-fluorescence in situ hybridization |
| haemangioendothelioma tuberosum multiplex | An eruption of pinkish papules, caused by hyperplasia of the endothelium of the superficial blood vessels. (05 Mar 2000) |
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| lymphangioma tuberosum multiplex | A cutaneous lesion characterised by multiple, slightly red, cystlike nodules (located chiefly on the trunk), resulting from fairly large lymphatic vessels and spaces, and groups of proliferating endothelial cells; the lesion has some gross resemblance to spiradenoma, except for the characteristic location. (05 Mar 2000) |
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| haemangioendothelioma | <oncology, tumour> A tumour which comes from endothelial cells lining the inside surfaces of blood vessels. (09 Oct 1997) |
| haemangioendothelioma, epithelioid | A tumour of medium-to-large veins, composed of plump-to-spindled endothelial cells that bulge into vascular spaces in a tombstone-like fashion. These tumours are thought to have "borderline" aggression, where one-third develop local recurrences, but only rarely metastasize. It is unclear whether the epithelioid haemangioendothelioma is truly neoplastic or an exuberant tissue reaction, nor is it clear if this is equivalent to kimura's disease (see angiolymphoid hyperplasia with eosinophilia). (12 Dec 1998) |
| xanthoma tuberosum | Xanthomatosis associated with familial type II, and occasionally type III, hyperlipoproteinaemia. Synonym: xanthoma tuberosum simplex. (05 Mar 2000) |
| xanthoma tuberosum simplex | Xanthomatosis associated with familial type II, and occasionally type III, hyperlipoproteinaemia. Synonym: xanthoma tuberosum simplex. (05 Mar 2000) |
| liver haemangioendothelioma | <radiology> Females (67%), infants (90% before 6 m/o), symptoms: mass (hepatomegaly), cutaneous haemangiomas (45%), mildly increased aFP (occasionally), with or without congestive heart failure secondary to shunting (only 4%), usually diffuse, precludes surgery, most involute spontaneously or with steroids Differential diagnosis: mesenchymal hamartoma, cavernous haemangioma, hepatoma, hepatoblastoma (increased aFP), metastatic neuroblastoma (increased serum VMA) (12 Dec 1998) |
| arthrogryposis multiplex congenita | Limitation of range of joint motion and contractures present at birth, usually involving multiple joints; a syndrome probably of diverse aetiology that may result from changes in spinal cord, muscle, or connective tissue. Several forms exist, autosomal dominant, recessive, and X-linked. Synonym: amyoplasia congenita. (05 Mar 2000) |
| paramyoclonus multiplex | Synonym: myoclonus multiplex. Origin: para-+ G. Mys, muscle, + klonos, a tumult (05 Mar 2000) |
| mononeuritis multiplex | <endocrinology, neurology> A condition characterised by inflammation of several nerves in unrelated portions of the body, may be seen in association with long-standing diabetes. (27 Sep 1997) |
| myoclonus multiplex | An ill-defined disorder marked by rapid and widespread muscle contractions. Synonym: paramyoclonus multiplex, polyclonia, polymyoclonus. (05 Mar 2000) |
| xanthoma multiplex | <dermatology, pathology> An accumulation of an excess of lipids in the body due to disturbance of lipid metabolism and marked by the formation of foam cells in skin lesions. (16 Dec 1997) |
| steatocystoma multiplex | Widespread, multiple, thin-walled cysts of the skin that are lined by squamous epithelium, including lobules of sebaceous cells. (05 Mar 2000) |
| dysostosis multiplex | <syndrome> Mucopolysaccharidosis in which there is a deficiency of alpha-l-iduronidase, an accumulation of an abnormal intracellular material, and excretion of dermatan sulfate and heparan sulfate in the urine; with severe abnormality in development of skeletal cartilage and bone, with dwarfism, kyphosis, deformed limbs, limitation of joint motion, spadelike hand, corneal clouding, hepatosplenomegaly, mental retardation, and gargoyle-like facies; autosomal recessive inheritance. See: mucolipidosis. Synonym: dysostosis multiplex, Hurler's disease, lipochondrodystrophy, Pfaundler-Hurler syndrome, type IH mucopolysaccharidosis. (05 Mar 2000) |
| dysplasia epiphysialis multiplex | A dominantly inherited abnormality of epiphyses characterised by difficulty in walking, pain and stiffness of joints, stubby fingers, and often dwarfism of short-limb type; on X-ray examination, the epiphyses are mottled and irregular; ossification centres are late in appearance and may be multiple, but the vertebrae are normal. There is also an autosomal recessive form . Synonym: dysplasia epiphysialis multiplex. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|