| ICO | idiopathic cyclic oedema; impedance cardiac output |
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| AILD | Angio-Immunoblastic Lymphadenopathy with Dysproteinemia |
| Angio | angiography, angiogram, angiographic |
| AHC | Albright's Hereditary Osteodystrophy |
| AHO | Albright's Hereditary Osteodystrophy |
| HANE | Hereditary Angio Neurotic Edema |
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| HAE | Hereditary Angio-Edema |
| CMO | cystoid macular oedema |
| A.I.L. | Angio-immunoblastic lymphadenopathy |
| AILD | Angio-immunoblastic lymphadenopathy |
| 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) |
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| angioneurotic oedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioedema. (12 Dec 1998) |
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| hereditary angioneurotic oedema | A genetic form of angioedema. (angioedema is also referred to as quinke's disease.) persons with it are born lacking an inhibitor protein (called c1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of c1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioedema. (12 Dec 1998) |
| oedema, hereditary angioneurotic | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioedema. (12 Dec 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) |
| ambulant oedema | Oedema forming during periods of walking with the legs dependent. (05 Mar 2000) |
| angioneurotic oedema | <neurology> An acute or recurring attack of transient oedema suddenly appearing in areas of the skin or mucous membranes and occasionally of the viscera, often associated with dermatographism, urticaria, erythema, and purpura. It can produce dramatic swelling of the subcutaneous tissues (welts beneath the skin) that typically appears around the eyes and lips. Welts may also involve the hands, feet and throat (compromise the airway). This condition is associated with allergies (for example foods, pollen), but may also be a side effect of some medications (for example ACE inhibitors, salicylates). Emotional stress, exposure to cold, water, sunlight, heat and insect bites all have been know to cause angioneurotic oedema. Treatment is with adrenaline, antihistamines, cimetidine, and/or corticosteroids. (12 Dec 1998) |
| Berlin's oedema | Retinal oedema after blunt trauma to the globe. (05 Mar 2000) |
| blue oedema | The swelling and cyanosis of an extremity in hysterical paralysis. (05 Mar 2000) |
| brain oedema | Brain swelling due to increased volume of the extravascular compartment from the uptake of water in the neuropile and white matter. See: brain swelling. Synonym: brain oedema. (05 Mar 2000) |
| brawny oedema | Swelling of subcutaneous tissues which cannot be indented by compression easily. Usually due to metabolic abnormality, such as increased glycosaminoglycan content, like that which occurs in Graves' disease (pretibial myxoedema) or in early phase of scleroderma. Synonym: brawny oedema. (05 Mar 2000) |
| brown oedema | Oedema of the lungs associated with chronic passive congestion. (05 Mar 2000) |
| bullous oedema | A reddened, swollen appearance of the ureteral orifice in the bladder wall, frequently observed with distal ureteral calculi or in tuberculosis of the ureter. (05 Mar 2000) |
| bullous oedema vesicae | A prominent area of focal oedema involving the bladder mucosa, consisting of elevated masses of edematous tissue or clusters of clear fluid-filled vesicles; often associated with chronic inflammation or irritation secondary to tubes, foreign bodies, or perivesical inflammation. (05 Mar 2000) |
| cachectic oedema | Oedema occurring in diseases characterised by wasting and hypoproteinaemia; due to low plasma oncotic pressure. Synonym: marantic oedema. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|