| 영문 | herpes simplex | 한글 | 단순헤르페스 |
|---|---|---|---|
| 설명 | 급성 바이러스 감염증의 하나. 직경 3~6mm의 작은물집이 집단으로 피부에 나타는 것이 특징이다. 가끔 입술이나 콧구멍의 주위에 또는 성기에 생긴다. 보통 발열을 수반하나, 감기, 피부박탈, 감정적 불안 등을 수반하는 일이 많다. 단순히 헤르페스라고도 부른다. 단순헤르페스는 직접적인 접촉, 음부헤르페스는 성접촉이나 출생시 산도를 통해서 감염된다. 이들 병변의 병리학적 특징은 핵내에서 바이러스가 증식함에 따라 카우드리 A형 핵내 포함체를 형성한다. |
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| EBA | epidermolysis bullosa acquisita; epidermolysis bullosa atrophicans; orthoethoxybenzoic acid |
|---|---|
| DEBS | dominant epidermolysis bullosa simplex |
| EBS | elastic back strap; electric brain stimulation; Emergency Bed Service; epidermolysis bullosa simplex... |
| DEB | diepoxybutane; diethylbutanediol; Division of Environmental Biology; dystrophic epidermolysis bullos... |
| EB | elective abortion; electron beam; elementary body; emotional behavior; endometrial biopsy; epidermol... |
| EBS | Epidermolysis Bullosa Simplex |
|---|---|
| DEB | Dystrophic Epidermolysis Bullosa |
| EB | Epidermolysis Bullosa |
| EBA | Epidermolysis bullosa acquisita |
| GABEB | Generalised atrophic benign epidermolysis bullosa |
| 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) |
|---|---|
| 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) |
| adynamia episodica hereditaria | Hyperkalaemic periodic paralysis, without myotonia. (05 Mar 2000) |
| porphyria cutanea tarda hereditaria | A form of hepatic porphyria (porphyria, hepatic) characterised by photosensitivity resulting in bullae that rupture easily to form shallow ulcers. This condition occurs in two forms: a sporadic, nonfamilial form that begins in middle age and has normal amounts of uroporphyrinogen decarboxylase with diminished activity in the liver; and a familial form in which there is an autosomal dominant inherited deficiency of uroporphyrinogen decarboxylase in the liver and red blood cells. (12 Dec 1998) |
| protocoproporphyria hereditaria | Porphyria characterised by abdominal pain and neuropsychiatric abnormalities, by dermal sensitivity to light and mechanical trauma, by increased faecal excretion of proto-and coproporphyrin, and by increased urinary excretion of d-aminolevulinic acid, porphobilinogen, and porphyrins; due to a deficiency of protoporphyrinogen oxidase; autosomal dominant inheritance. Synonym: protocoproporphyria hereditaria, South African type porphyria. (05 Mar 2000) |
| syphilis hereditaria | <radiology> Wimberger sign, periostitis, part of ToRCHS complex (12 Dec 1998) |
| syphilis hereditaria tarda | Syphilis, believed to be congenital, but not manifesting itself until several years after birth. (05 Mar 2000) |
| epidermolysis | A condition in which the epidermis is loosely attached to the corium, readily exfoliating or forming blisters. Origin: epidermis + G. Lysis, loosening (05 Mar 2000) |
| 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) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|