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A Dilated Cardiomyopathy Revealing a Neuroblastoma: Which Link?
Duhil de Bénazé, Gwenaelle; Iserin, Franck; Durand, Philippe; Schleiermacher, Gudrun; Orbach, Daniel.
Afiliação
  • Duhil de Bénazé G; *Department of Paediatric, Adolescent and Young Adult Oncology, Institut Curie †Department of Cardiology, Necker Hospital, Assistance Publique Hôpitaux de Paris, Paris ‡Pediatric Intensive Care and Neonatal Medicine, Paris South University Hospitals, Assistance Publique Hôpitaux de Paris, Le Kremlin-Bicêtre, France.
J Pediatr Hematol Oncol ; 38(7): e251-3, 2016 10.
Article em En | MEDLINE | ID: mdl-27571126
ABSTRACT
Acute cardiac dysfunctions associated to neuroblastoma have rarely been reported. Cases already described are mainly related to high blood pressure, and rarely to an "acute catecholamine cardiomyopathy" more frequently found in adults with pheochromocytoma or secreting paraganglioma. We here report a case of an 8-month-old infant with severe acute cardiac failure with dilated cardiomyopathy and moderate ischemic myocardial signs, revealing a favorable histoprognosis neuroblastoma. After specific treatment, evolution was favorable, and cardiac function completely recovered. The association of reversible ischemic signs with high plasmatic level of catecholamines suggests the existence of a catecholamine-induced acute cardiac dysfunction which imitates a Tako-Tsubo syndrome in neuroblastoma.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cardiomiopatia Dilatada / Neuroblastoma Tipo de estudo: Etiology_studies Limite: Humans / Infant / Male Idioma: En Revista: J Pediatr Hematol Oncol Assunto da revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cardiomiopatia Dilatada / Neuroblastoma Tipo de estudo: Etiology_studies Limite: Humans / Infant / Male Idioma: En Revista: J Pediatr Hematol Oncol Assunto da revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: França