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기저세포모반증후군과 관련 없이 발생한 피부각질낭 1예

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Author(s)
이혜원박지영강선희최미선
Keimyung Author(s)
Lee, Hye WonChoe, Mi SunKang, Sun Hee
Department
Dept. of Pathology (병리학)
Dept. of Surgery (외과학)
Journal Title
Korean Journal of Pathology
Issued Date
2011
Volume
45
Issue
3
Keyword
KeratocystsNevoid basal cell carcinoma syndromeSkin
Abstract
A cutaneous keratocyst is very rare and is ordinarily associated with nevoid basal cell carcinoma syndrome (NBCCS), also known as Gorlin syndrome. NBCCS is a rare autosomal-dominant disorder that results from the mutation in the patched homologue 1 (PTCH1) gene located on chromosome 9q22.3, with high penetrance and variable expressivity. NBCCS demonstrates multisystem manifestations such as multiple basal cell carcinomas in early age, jaw cysts and pits of the hands and feet. Cutaneous keratocysts are characteristically lined by festooned keratinized squamous epithelium with parakeratosis. The cystic wall contains neither granular cell layer nor skin appendages. To the best of our knowledge, only two cases of cutaneous keratocysts not associated with NBCCS have been reported to date. We report one another case of a histologically confirmed cutaneous keratocyst in a 50-year-old female without a family history and clinical features of NBCCS.
Alternative Title
Sporadic Cutaneous Keratocyst without Nevoid Basal Cell Carcinoma Syndrome - Report of 1 Case -
Keimyung Author(s)(Kor)
이혜원
최미선
강선희
Publisher
School of Medicine
Citation
이혜원 et al. (2011). 기저세포모반증후군과 관련 없이 발생한 피부각질낭 1예. Korean Journal of Pathology, 45(3), 322–325. doi: 10.4132/KoreanJPathol.2011.45.3.322
Type
Article
ISSN
1738-1843
DOI
10.4132/KoreanJPathol.2011.45.3.322
URI
https://kumel.medlib.dsmc.or.kr/handle/2015.oak/33736
Appears in Collections:
1. School of Medicine (의과대학) > Dept. of Pathology (병리학)
1. School of Medicine (의과대학) > Dept. of Surgery (외과학)
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