| 영문 | syphilis | 한글 | 매독 |
|---|---|---|---|
| 설명 | 매독은 매독균(Treponema pallidum)이라는 균에 의한 전염병으로 대부분이 성교를 통해 감염되며 드물게 키스, 수혈 등에 의하여 감염될 수도 있고 모체에서 태반을 통하여 태아에게 감염될 수도 있다. |
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| 영문 | congenital syphilis | 한글 | 선천매독 |
|---|---|---|---|
| 설명 | 임부가 매독에 감염되어 있으면 임신 후기에 매독균이 태반을 통해 혈행성으로 태아에 감염(수직감염)된 것을 말하다. 대부분은 유산, 사산이 되지만 출생하면 제2기 이후의 발진을 보인다. 발현시기에 따라서 ① 태아매독, ② 유아매독, ③ 만발성 선천매독으로 분류된다. ①에서는 뼈연골염, 간-지라 비대와 매독성 천포창, ②에서는 파로가성마비와 매독성 코염, ③에서는 허친슨 세징후(허친슨 치아, 속귀성 난청, 실질성 각막염)에 따라 특징이 있다. 기타 수두증, 지능발육 불량 등을 자주 볼 수 있다. 매독 혈청반응은 대부분의 경우 양성으로 나온다. 매우 드물게 간세포내에서 매독균을 무수히 볼 수 있다. 간세포 주변의 섬유화와 함께 불규칙한 흉터(hepar lobatum)를 만들 수 있다. |
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| STS | sequence tagged site; serologic test for syphilis; sodium tetradecyl sulfate; sodium thiosulfate; st... |
|---|---|
| GOH | geroderma osteodysplastica hereditaria |
| KHM | keratoderma hereditaria mutilans |
| LH | late healing; lateral hypothalamic [syndrome]; left hand; left heart; left hemisphere; left hyperpho... |
| THH | telangiectasia hereditaria haemorrhagica; trichohyalin |
| CS | Congenital syphilis |
|---|---|
| PCT | Porphyria Cutanea Tarda |
| syphilis hereditaria tarda | Syphilis, believed to be congenital, but not manifesting itself until several years after birth. (05 Mar 2000) |
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| 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) |
|---|---|
| syphilis hereditaria | <radiology> Wimberger sign, periostitis, part of ToRCHS complex (12 Dec 1998) |
| adynamia episodica hereditaria | Hyperkalaemic periodic paralysis, without myotonia. (05 Mar 2000) |
| 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) |
| rachitis tarda | <pathology> A condition marked by softening of the bones (due to impaired mineralisation, with excess accumulation of osteoid), with pain, tenderness, muscular weakness, anorexia and loss of weight, resulting from deficiency of vitamin D and calcium. Origin: Gr. Malakia = softness (18 Nov 1997) |
| porphyria cutanea tarda | 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) |
| porphyria cutanea tarda symptomatica | 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) |
| neurosis tarda | Neurotic patterns developing in older people, related to organic cerebral lesions. (05 Mar 2000) |
| dentia tarda | Delayed tooth eruption. Origin: L. Delayed (05 Mar 2000) |
| cardiovascular syphilis | Involvement of the cardiovascular system seen in late syphilis, usually resulting in aortitis, aneurysm formation, and aortic valvular insufficiency. (05 Mar 2000) |
| meningovascular syphilis | A rare manifestation of secondary or tertiary syphilis characterised by mild, nonsuppurative, chronic inflammation of the leptomeninges and an intracranial or spinal angiitis. (05 Mar 2000) |
| congenital syphilis | <radiology> Wimberger sign, periostitis, part of ToRCHS complex (12 Dec 1998) |
| primary syphilis | The first stage of syphilis See: syphilis. (05 Mar 2000) |
| hereditary syphilis | Synonym: congenital syphilis. (05 Mar 2000) |
| secondary syphilis | The second stage of syphilis See: syphilis. Synonym: mesosyphilis. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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