TY - JOUR
T1 - Recurrent Protein-losing Enteropathy and Tricuspid Valve Insufficiency in a Transplanted Heart
T2 - A Causal Relationship?
AU - Aggarwal, Sanjeev
AU - Delius, Ralph E.
AU - Walters, Henry L.
AU - L'Ecuyer, Thomas J.
PY - 2012/5
Y1 - 2012/5
N2 - 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.
AB - 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.
KW - Heart transplantation
KW - Protein-losing enteropathy
KW - Tricuspid valve regurgitation
UR - http://www.scopus.com/inward/record.url?scp=84861545121&partnerID=8YFLogxK
U2 - 10.1111/j.1747-0803.2011.00557.x
DO - 10.1111/j.1747-0803.2011.00557.x
M3 - Article
C2 - 21801319
AN - SCOPUS:84861545121
SN - 1747-079X
VL - 7
SP - E10-E13
JO - Congenital Heart Disease
JF - Congenital Heart Disease
IS - 3
ER -