Cowden 증후군 환자에서 발생한 캔디다 식도염 1예
- Author(s)
- 강경지; 윤혜정; 류성렬; 류남희; 강유나; 황진복; Kyung Ji Kang; Hye Jung Yun; Seong-Yeol Ryu; Nam-Hee Ryoo; Yu Na Kang; Jin-Bok Hwang
- Keimyung Author(s)
- Hwang, Jin Bok; Ryu, Seong Yeol; Ryoo, Nam Hee; Kang, Yu Na
- Department
- Dept. of Pediatrics (소아청소년학)
Dept. of Internal Medicine (내과학)
Dept. of Laboratory Medicine (진단검사의학)
Dept. of Pathology (병리학)
- Journal Title
- 대한소아소화기영양학회지
- Issued Date
- 2009
- Volume
- 12
- Issue
- 1
- Abstract
- Cowden's syndrome is a harmatomatous polyposis syndrome with characteristic mucocutaneous lesions and among the spectra of clinical disorders that has been attributed to germline mutations in the PTEN gene. Although Cowden’s syndrome has rarely been reported, immunologic studies have revealed that patients with this syndrome have humoral and/or cellular immune abnormalities. We recently identified a 21-year-old woman with Cowden's syndrome who was diagnosed with candida esophagitis without a history of diabetes, carcinoma, or steroid therapy. We report the immunologic status of this patient and the relationship with candida esophagitis on the basis of a literature review.
Cowden 증후군으로 진단되어 추적 관찰 중인 21세 여자에서 위장관 용종의 정기적 관찰을 위하여 시행한 내시경 검사 중 캔디다 식도염이 발견되어 문헌 고찰과 함께 보고한다. 면역학적 이상, 진균 식도 감염의 선행 질환, 투약의 병력이 없었고, 뚜렷한 식도 감염의 임상 증
상도 없었다.
- 공개 및 라이선스
-
- 파일 목록
-
Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.