| 영문 | purpura | 한글 | 자색반증 |
|---|---|---|---|
| 설명 | 피부내의 출혈로 인하여, 피부 표피를 통하여 쉽게 보이는 자홍색 혹은 적갈색 반점을 특징으로 하는 일련의 질환을 총칭하는 용어이다. 대개 홍반과 구별해야 하는 데 홍반은 피부밑의 혈관이 팽창하여 붉게 보이는 현상으로 투명한 자를 이용하여 피부를 눌러서 관찰해보면 쉽게 구별이 가능하다. 이때 홍반은 붉은 색이 없어지지만, 자반은 붉은 색이 없어지지 않는다. |
||
| EBA | epidermolysis bullosa acquisita; epidermolysis bullosa atrophicans; orthoethoxybenzoic acid |
|---|---|
| ITP | idiopathic thrombocytopenic purpura; immune thrombocytopenia; immunogenic thrombocytopenic purpura; ... |
| DEB | diepoxybutane; diethylbutanediol; Division of Environmental Biology; dystrophic epidermolysis bullos... |
| DEBS | dominant epidermolysis bullosa simplex |
| EB | elective abortion; electron beam; elementary body; emotional behavior; endometrial biopsy; epidermol... |
| DEB | Dystrophic Epidermolysis Bullosa |
|---|---|
| EB | Epidermolysis Bullosa |
| EBS | Epidermolysis Bullosa Simplex |
| EBA | Epidermolysis bullosa acquisita |
| GABEB | Generalised atrophic benign epidermolysis bullosa |
| concha bullosa | Abnormal pneumatization of the middle turbinate which may interfere with normal ventilation of sinus ostia and can result in recurrent sinusitis. (05 Mar 2000) |
|---|---|
| Pseudostertagia bullosa | One of the medium stomach worms located in the abomasum of sheep, goats, and pronghorn; it is found chiefly in the western U.S. (05 Mar 2000) |
| impetigo bullosa | Impetigo with lesions of large size, forming bullae. (05 Mar 2000) |
| impetigo contagiosa bullosa | Discrete purulent skin lesions occasionally seen with streptococcal pyoderma. (05 Mar 2000) |
| epidermolysis bullosa | This represents a group of rare inherited disorders in which blistering of the skin occurs in response to skin trauma. Large fluid-filled blisters can occur in response to injury, skin rubbing, chafing or even increases in room temperature. Secondary bacterial infection of the blisters is common. Complications include oesophageal stricture, infections, loss of function of hands and feet and malnutrition. The dermatologist is the expert in the evaluation and treatment of this disorder. (27 Sep 1997) |
| epidermolysis bullosa acquisita | Form of epidermolysis bullosa characterised by trauma-induced, subepidermal blistering with no family history of the disease. Direct immunofluorescence shows IgG deposited at the dermo-epidermal junction. (12 Dec 1998) |
| epidermolysis bullosa dystrophica | Form of epidermolysis bullosa characterised by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. (12 Dec 1998) |
| epidermolysis bullosa, junctional | Form of epidermolysis bullosa having onset at birth or during the neonatal period and transmitted through autosomal recessive inheritance. It is characterised by generalised blister formation, extensive denudation, and separation and cleavage of the basal cell plasma membranes from the basement membrane. (12 Dec 1998) |
| epidermolysis bullosa lethalis | Epidermolysis bullosa in which the bullae are persistent, nonhealing, and often present in the oral mucosa and trachea, but not on the palms and soles, leading to death. Synonym: epidermolysis bullosa, junctional type, Herlitz syndrome. (05 Mar 2000) |
| epidermolysis bullosa simplex | This represents a group of rare inherited disorders in which blistering of the skin occurs in response to skin trauma. Large fluid-filled blisters can occur in response to injury, skin rubbing, chafing or even increases in room temperature. Secondary bacterial infection of the blisters is common. Complications include oesophageal stricture, infections, loss of function of hands and feet and malnutrition. The dermatologist is the expert in the evaluation and treatment of this disorder. (27 Sep 1997) |
| urticaria bullosa | An eruption of wheals capped with subepidermal vesicles. Synonym: urticaria vesiculosa. (05 Mar 2000) |
| acute vascular purpura | <dermatology> This relatively rare disorder is characterised by skin purpura, joint pains, abdominal pain and renal disease (glomerulonephritis). Although Henoch-Schonlein purpura or anaphylactoid purpura, is thought to be a immune complex mediated disease, its exact cause is unknown. Its typical benign coarse can, however, include renal failure. (27 Sep 1997) |
| allergic purpura | Nonthrombocytopenic purpura due to sensitization to foods, drugs, and insect bites. Synonym: anaphylactoid purpura. (05 Mar 2000) |
| anaphylactoid purpura | <dermatology> This relatively rare disorder is characterised by skin purpura, joint pains, abdominal pain and renal disease (glomerulonephritis). Although Henoch-Schonlein purpura or anaphylactoid purpura, is thought to be a immune complex mediated disease, its exact cause is unknown. Its typical benign coarse can, however, include renal failure. (27 Sep 1997) |
| autoimmune thrombocytopenia purpura | <haematology> A rare autoimmune disorder characterised by an acute shortage of platelets with resultant bruising and spontaneous bleeding. The platelet count becomes exceedingly low and spontaneous bleeding from the gums, gastrointestinal tract and nose can be seen. Physical examination may demonstrate enlargement of the spleen. A typical rash occurs to do microscopic haemorrhage of small blood vessels in the skin. Platelet counts under 10,000 can lead to spontaneous haemorrhage into the brain causing death. Treatment with corticosteroids is generally effective. Surgical removal of the spleen (splenectomy) is reserved for some patients. Anti-platelet antibodies are detectable in some cases. It may present in either an acute or a chronic form. Acronym: ITP (20 Sep 2002) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|