| AILD | Angio-Immunoblastic Lymphadenopathy with Dysproteinemia |
|---|---|
| Angio | angiography, angiogram, angiographic |
| A.I.L. | Angio-immunoblastic lymphadenopathy |
|---|---|
| AILD | Angio-immunoblastic lymphadenopathy |
| A.I.L.D. | Angio-immunoblastic lymphadenopathy with dysproteinaemia |
| HANE | Hereditary Angio Neurotic Edema |
| HAE | Hereditary Angio-Edema |
| lith | A joint or limb; a division; a member; a part formed by growth, and articulated to, or symmetrical with, other parts. Origin: AS. Li. Source: Websters Dictionary (01 Mar 1998) |
|---|---|
| angio- | <prefix> A prefix, or combining form, in numerous compounds, usually relating to seed or blood vessels, or to something contained in, or covered by, a vessel. Origin: Gr. Vessel receptacle. (29 Oct 1998) |
| angio-osteohypertrophy syndrome | <syndrome> A congenital malformation syndrome characterised by the triad of asymmetric limb hypertrophy, haemangiomata, and nevi. Asymmetric limb hypertrophy is enlargement of one limb and not the corresponding limb on the other side, the enlarged limb being 3 times more likely to be a leg than an arm in ktw; and the limb enlargement is of bone as well as soft tissue. The haemangiomas, abnormal nests of blood vessels that proliferate inappropriately and excessively, cover a remarkable range from small innocuous capillary haemangiomas ( strawberry marks ) to huge cavernous haemangiomas. The nevi are pigmented moles on the skin; in ktw there are often also dark linear streaks on the skin, streaks due to too much pigment. There can be other abnormalities but the triad is the consistent clinical centrepiece of the disease. most persons with ktw have an enlarged leg and do relatively well without treatment or, for example, with only compression from an elastic stocking. Skin ulcers and other skin problems can occur over the swollen leg. Usually, the treatment is conservative. Surgery is almost never needed. The only possible exceptions are the very rare situations in which the leg reaches gigantic proportions or secondary clotting difficulties arise (due to trapping and destruction of blood platelets in a huge haemangioma). Then, amputation may become necessary. The cause of ktw syndrome is unknown. (12 Dec 1998) |
| hereditary angio oedema | <biochemistry> Condition in which there seems to be uncontrolled production of C2 kinin because of a deficiency in C1 inhibitor levels. (18 Nov 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|