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Rapid reversal of dilated cardiomyopathy following removal of neuroblastoma

Published online by Cambridge University Press:  19 August 2008

Luca Rosti ,
Pierluigi Festa  and
Carlo Corbetta
Luca Rosti*
Affiliation:
Department of Pediatrics and Neonatology, Istituti Clinici di Perfezionamento, Regina Elena Hospital, Milan, Italy Department of Cardiology / Cardiac Surgery, San Donato Hospital, San Donato Milanese, Milan, Italy
Pierluigi Festa
Affiliation:
Department of Cardiology / Cardiac Surgery, San Donato Hospital, San Donato Milanese, Milan, Italy
Carlo Corbetta
Affiliation:
Laboratorio, Istituti Clinici di Perfezionamento, Milan, Italy
*
Dr Luca Rosti, ICP-Ospedale Regina Elena, via Manfredo Fanti 6, 1–20122, Milan, Italy. Fax:39 0255185109
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Abstract

Reported is a child with dilated cardiomyopathy, in whom medical therapy resulted in a mild improvement of cardiac function. Metabolic studies suggested the presence of a catecholamine-secreting tumour; and an adrenal neuroblastoma was identified and surgically removed. Following surgery, there was progressive and complete normalization of cardiac function. Although very rare, neurogenic tumours may be involved in the development of a dilated cardiomyopathy in the infant and child.

Keywords

Dilated cardiomyopathyneuroblastomacatecholamine cardiomyopathychildren
Type
Brief Reports
Information
Cardiology in the Young , Volume 9 , Issue 5 , September 1999 , pp. 519 - 521
Copyright
Copyright © Cambridge University Press 1999

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