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Pediatric split liver transplantation after Fontan procedure in left isomerism combined with biliary atresia: A case report
- Youn, Joong Kee;
- Lee, Jeong-Moo;
- Yi, Nam-Joon;
- Choi, Young Rok;
- Suh, Suk-Won;
- 외 9명
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7초록
LI is a subset of the heterotaxy syndrome and a rare birth defect that involves the heart and other organs. It can be combined with extracardiac abnormalities, especially BA. CHD can be associated with LI in up to 15% of cases, although it is rare in BA. Pediatric LT for a child with ESLD due to BA combined with LI and CHD is a challenging issue for a transplant surgeon. Herein, we report a successful split LT on a three-yr-old boy with LI who survived after a Fontan procedure due to single ventricle, but who suffered from HPS associated with BA.
키워드
biliary atresia; left isomerism; Fontan operation; hepatopulmonary syndrome; liver transplantation; SITUS-INVERSUS; HEPATOPULMONARY SYNDROME; OPERATION; MORTALITY; SURGERY; COMPLICATIONS; CIRCULATION; PREDICTORS; OUTCOMES; CHILDREN
- 제목
- Pediatric split liver transplantation after Fontan procedure in left isomerism combined with biliary atresia: A case report
- 저자
- Youn, Joong Kee; Lee, Jeong-Moo; Yi, Nam-Joon; Choi, Young Rok; Suh, Suk-Won; You, Tae; Lee, Kwang-Woong; Jung, Chul-Woo; Lee, Ji-won; Bae, Eun-Jung; Ko, Jae Sung; Kim, Woong-Han; Park, Kwi-Won; Suh, Kyung-Suk
- 발행일
- 2014-12
- 유형
- Article
- 권
- 18
- 호
- 8
- 페이지
- E274 ~ E279
- 언어
- ENG
- 출판사
- WILEY-BLACKWELL
- 발행국가
- 미국
- ISSN
- E 1399-3046
P 1397-3142