Restrictive Cardiomyopathy in a Child

Restrictive cardiomyopathy in young children is rare and carries a poor prognosis. We report an 18-month-old girl with poor feeding and abdominal distension. Except for hepatomegaly, no other gastrointestinal abnormalities were found. She had normalsized ventricles but biatrial enlargement. Echocard...

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Main Authors: Shan-Miao Lin, Haw-Kwei Hwang, Ming-Ren Chen
Format: Article
Language:English
Published: Elsevier 2008-04-01
Series:Pediatrics and Neonatology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1875957208600121
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author Shan-Miao Lin
Haw-Kwei Hwang
Ming-Ren Chen
author_facet Shan-Miao Lin
Haw-Kwei Hwang
Ming-Ren Chen
author_sort Shan-Miao Lin
collection DOAJ
description Restrictive cardiomyopathy in young children is rare and carries a poor prognosis. We report an 18-month-old girl with poor feeding and abdominal distension. Except for hepatomegaly, no other gastrointestinal abnormalities were found. She had normalsized ventricles but biatrial enlargement. Echocardiography demonstrated normal systolic but impaired diastolic function. Cardiac catheterization revealed a characteristic dip-and-plateau configuration of the right ventricular pressure tracing. The diagnosis turned out to be typical restrictive cardiomyopathy. The patient was maintained on aspirin while awaiting cardiac transplant.
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spelling doaj.art-38f59bec23124a6783412798641ffb582022-12-22T03:15:42ZengElsevierPediatrics and Neonatology1875-95722008-04-01492485110.1016/S1875-9572(08)60012-1Restrictive Cardiomyopathy in a ChildShan-Miao Lin0Haw-Kwei Hwang1Ming-Ren Chen2Department of Pediatrics, Mackay Memorial Hospital, Taipei, TaiwanDepartment of Pediatrics, Mackay Memorial Hospital, Taipei, TaiwanDepartment of Pediatrics, Mackay Memorial Hospital, Taipei, TaiwanRestrictive cardiomyopathy in young children is rare and carries a poor prognosis. We report an 18-month-old girl with poor feeding and abdominal distension. Except for hepatomegaly, no other gastrointestinal abnormalities were found. She had normalsized ventricles but biatrial enlargement. Echocardiography demonstrated normal systolic but impaired diastolic function. Cardiac catheterization revealed a characteristic dip-and-plateau configuration of the right ventricular pressure tracing. The diagnosis turned out to be typical restrictive cardiomyopathy. The patient was maintained on aspirin while awaiting cardiac transplant.http://www.sciencedirect.com/science/article/pii/S1875957208600121cardiac catheterizationchildrestrictive cardiomyopathy
spellingShingle Shan-Miao Lin
Haw-Kwei Hwang
Ming-Ren Chen
Restrictive Cardiomyopathy in a Child
Pediatrics and Neonatology
cardiac catheterization
child
restrictive cardiomyopathy
title Restrictive Cardiomyopathy in a Child
title_full Restrictive Cardiomyopathy in a Child
title_fullStr Restrictive Cardiomyopathy in a Child
title_full_unstemmed Restrictive Cardiomyopathy in a Child
title_short Restrictive Cardiomyopathy in a Child
title_sort restrictive cardiomyopathy in a child
topic cardiac catheterization
child
restrictive cardiomyopathy
url http://www.sciencedirect.com/science/article/pii/S1875957208600121
work_keys_str_mv AT shanmiaolin restrictivecardiomyopathyinachild
AT hawkweihwang restrictivecardiomyopathyinachild
AT mingrenchen restrictivecardiomyopathyinachild