Aggarwal Sanjeev, Delius Ralph E, Walters Henry L, L'Ecuyer Thomas J
Division of Pediatric Cardiology Department of Cardiovascular Surgery, Children's Hospital of Michigan, 3901 Beaubien Blvd., Detroit, MI 48201, USA.
Congenit Heart Dis. 2012 May-Jun;7(3):E10-3. doi: 10.1111/j.1747-0803.2011.00557.x. Epub 2011 Jul 31.
This case report describes a toddler who developed a protein-losing enteropathy (PLE) 4 years after orthotopic heart transplantation (OHT). He was born with a hypoplastic left heart syndrome for which he underwent a successful Norwood procedure, a Hemi-Fontan palliation, and a Fontan palliation at 18 months of age. Fifteen months following the Fontan operation, he developed a PLE and Fontan failure requiring OHT. Four years after OHT, he developed a severe tricuspid regurgitation and a PLE. His PLE improved after tricuspid valve replacement. It is now 2 years since his tricuspid valve replacement and he remains clinically free of ascites and peripheral edema with a normal serum albumin level. His prosthetic tricuspid valve is functioning normally.
本病例报告描述了一名幼儿,其在原位心脏移植(OHT)4年后发生了蛋白丢失性肠病(PLE)。他出生时患有左心发育不全综合征,为此在18个月大时成功接受了诺伍德手术、半Fontan姑息手术和Fontan姑息手术。Fontan手术后15个月,他出现了PLE和Fontan衰竭,需要进行OHT。OHT 4年后,他出现了严重的三尖瓣反流和PLE。在更换三尖瓣后,他的PLE有所改善。自他更换三尖瓣至今已有2年,他临床上仍无腹水和外周水肿,血清白蛋白水平正常。他的人工三尖瓣功能正常。