| 영문 | acoustic neuroma, acoustic neurilemmoma | 한글 | 청신경초종 |
|---|---|---|---|
| 설명 | 청신경(제8뇌신경)의 신경겉을 싸고 있는 집(sheath)의 슈반세포(Schwann cell)에서 기원하는 종양-뇌종양 중 비교적 흔하며 대개 40~50대에 호발한다. 증상으로는 귀울림, 난청, 소뇌기능장애 등이 있으며, 이중 귀울림이 가장 초기의 증상이다. |
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| 영문 | neurofibromatosis | 한글 | 신경섬유종증 |
|---|---|---|---|
| 설명 | 전신의 여러곳에 무더기로 나는 신경섬유종을 특징으로 하는 유전성 전신 병. 말초 신경뿐 아니라 중추 신경계도 침범할 수 있다. 신경섬유종은 주로 전신의 피부에 발생되지만 신경얼기 혹은 내장에 생기는 수도 있다. 피부에는 또한 곳곳에 특유의 갈색색소반을 보게 된다. 골격의 변형을 일으킬 수도 있다. 신경초종이나 악성신경초종, 더욱이 신경교종이나 수막종 등의 두개내종양을 합병함도 알려져 있다. 1형(von Recklinghausen 병, 전형적 신경섬유종증)과 2형(중추형 또는 청각신경섬유종증)으로 구분한다. 전형적 신경섬유종증(1형)이 가장 많이 발생하며 다음과 같은 3가지 소견을 보인댜. 즉 ① 체표면, 체내 여러 곳에 산재되어 발생하는 얼기모양신경종, ② 우유커피반점, ③ 리쉬(Lisch) 결절로 불리는 홍채의 착색과오종이다. 2형은 1형보다 발생빈도가 적고, 특징적으로 양쪽성 청각신경종이 있으며, 우유반점은 보이나 리쉬결절은 없다. |
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| AS | acetylstrophanthidin; acidified serum; acoustic schwannoma; acoustic stimulation; active sarcoidosis... |
|---|---|
| BSE | behavior summarized evaluation; bilateral intranasal sphenoethmoiclectomy; bilateral symmetrical and... |
| BSO | bilateral sagittal osteotomy; bilateral salpingo-oophorectomy; British School of Osteopathy; butathi... |
| NF | nafcillin; National Formulary; nephritic factor; neurofibromatosis; neurofilament; neutral fraction;... |
| NF1 | neurofibromatosis type I; nuclear factor 1 |
| NF1 | NEUROFIBROMATOSIS TYPE 1 |
|---|---|
| NF | Neurofibromatosis |
| NF 1 | Neurofibromatosis |
| NF 1 | Neurofibromatosis 1 |
| NF 2 | Neurofibromatosis 2 |
| abortive neurofibromatosis | incomplete neurofibromatosis |
|---|---|
| genes, neurofibromatosis 1 | Tumour suppressor genes located on the long arm of human chromosome 17 in the region 17q11.2. Mutation of these genes is thought to cause neurofibromatosis 1. (12 Dec 1998) |
| genes, neurofibromatosis 2 | Tumour suppressor genes located on the long arm of human chromosome 22. Mutation or loss of these genes causes neurofibromatosis 2. (12 Dec 1998) |
| central type neurofibromatosis | Type I neurofibromatosis. Incomplete neurofibromatosis, multiple neurofibromas with minimal manifestations, perhaps limited to cafe-au-lait spots; individuals with minimal lesions may have offspring with severe involvement. Synonym: abortive neurofibromatosis. (05 Mar 2000) |
| neurofibromatosis | <oncology> One of the most common disorders in genetics, neurofibromatosis encompasses at least two diseases, designated NF-1 and NF-2. NF-1 or classic neurofibromatosis, is characterised by the familiar cafe- au-lait spots, axillary freckling, cutaneous and visceral neurofibromas (which sometimes undergo malignant transformation), gliomas, scoliosis, and Lisch nodules of the iris. NF-1 is associated with the the von Recklinghausen Neurofibromatosis locus that encodes the NF-1 protein, a GTPase activating protein which interacts with the ras proteins. The gene is located on chromosome 17. NF-2, also called acoustic or central neurofibromatosis, features neurofibromas restricted to the acoustic nerve (usually bilateral) and the central nervous system, skin lesions may or may not be present. The gene is located on chromosome 22. There are no biochemical markers of the disorder, but the cloning of both the NF-1 and NF-2 genes makes DNA-based diagnosis possible in some families. Both genes appear to be tumour suppressor genes. Both conditions are autosomal dominant, but the variable penetrance and expressivity and high frequency of new mutations make genetic counseling difficult. Inheritance: autosomal dominant. (29 Dec 1997) |
| neurofibromatosis 1 | A congenital autosomal dominant disorder characterised by developmental changes in the nervous system, muscles, bones, and skin especially in those derived from the embryonic neural crest. There are multiple cutaneous tumours and tumours of the peripheral and central nervous system. The disease has been linked to mutations of the nf1 gene on chromosome 17. (12 Dec 1998) |
| neurofibromatosis 2 | Severe autosomal dominant disorder characterised especially by bilateral acoustic neuromas as well as other multiple tumours including meningiomas, ependymomas, spinal neurofibromas, and gliomas. The disease has been linked to mutations of the nf2 gene on chromosome 22. (12 Dec 1998) |
| bilateral | <anatomy> Having two sides or pertaining to both sides. Origin: L. Latus = side (18 Nov 1997) |
| bilateral adrenal mass | <radiology> Acute granulomatous disease (e.g., TB), metastases (bilateral in 15%), pheochromocytoma (bilateral in 10%), adrenal hyperplasia (adenoma), spontaneous adrenal haemorrhage (12 Dec 1998) |
| bilateral hermaphroditism | True hermaphroditism with an ovotestis on both sides. (05 Mar 2000) |
| bilateral hydronephrosis | <nephrology, urology> Refers to the bilateral enlargement of the renal pelvis and calyces of the kidneys. This is not a disease itself but a finding associated with a variety of disease states which interfere with the drainage of urine from the kidneys to the ureters and into the bladder. Examples include acute and chronic bilateral obstructive uropathy, vesicoureteric reflux, ureteropelvic junction obstruction, neurogenic bladder, bladder outlet obstruction and prune belly syndrome. (27 Sep 1997) |
| bilateral large kidneys | <radiology> Autosomal dominant (adult) polycystic disease, lymphoma Cf: other urographic patterns (12 Dec 1998) |
| bilateral left-sidedness | A syndrome in which normally unpaired organs develop more symmetrically in mirror image; two spleens, one on each side, are usually present, and cardiovascular anomalies are common. Synonym: polysplenia syndrome. (05 Mar 2000) |
| bilateral mastectomy | <procedure, surgery> The surgical removal of both breasts. (09 Oct 1997) |
| bilateral medial orbital ecchymoses | <clinical sign, ophthalmology> The appearance of the eyes produced by subconjunctival haemorrhage and/or periorbital ecchymosis. Synonym: bilateral medial orbital ecchymoses. (21 Jun 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|