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Neonatal cardiogenic shock revealing obstructive cardiac Hibernoma: case report

BACKGROUND: Cardiac Hibernomas are very rare benign tumors and usually remain asymptomatic. Neonatal cardiogenic shock due to cardiac tumors is extremely very rare. Until this date a few cases of cardiac hibernoma have been reported in the literature. Transthoracic echocardiography help in the diffe...

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Autores principales: Gribaa, Rym, Kacem, Marwen, Ouannes, Sami, Majdoub, Wiem, Thabet, Houssem, Ali, Imen Ben, Elheraiche, Aymen, Slim, Mehdi, Hmissa, Sihem, Neffati, Elyes, Cherif, Taieb, Kortas, Chokri, Marah, Jamli, Jerbi, Sofiene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8340373/
https://www.ncbi.nlm.nih.gov/pubmed/34348738
http://dx.doi.org/10.1186/s13019-021-01582-z
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author Gribaa, Rym
Kacem, Marwen
Ouannes, Sami
Majdoub, Wiem
Thabet, Houssem
Ali, Imen Ben
Elheraiche, Aymen
Slim, Mehdi
Hmissa, Sihem
Neffati, Elyes
Cherif, Taieb
Kortas, Chokri
Marah, Jamli
Jerbi, Sofiene
author_facet Gribaa, Rym
Kacem, Marwen
Ouannes, Sami
Majdoub, Wiem
Thabet, Houssem
Ali, Imen Ben
Elheraiche, Aymen
Slim, Mehdi
Hmissa, Sihem
Neffati, Elyes
Cherif, Taieb
Kortas, Chokri
Marah, Jamli
Jerbi, Sofiene
author_sort Gribaa, Rym
collection PubMed
description BACKGROUND: Cardiac Hibernomas are very rare benign tumors and usually remain asymptomatic. Neonatal cardiogenic shock due to cardiac tumors is extremely very rare. Until this date a few cases of cardiac hibernoma have been reported in the literature. Transthoracic echocardiography help in the differential diagnosis, but the definitive diagnosis is histological. The management strategy is not clearly codified. The Aim is to report and discuss the clinical features of a cardiac Hibernoma and review the relevant literature. CASE PRESENTATION: We describe a case of a 2-day-old Caucasian full-term male neonate admitted in neonate intensive care with cardiogenic shock, having fluid resuscitation and inotropic drugs. Ventilatory support was started immediately with the subsequent reestablishment of normal blood pressure. Then he was transferred to the echocardiography laboratory. Transthoracic echocardiography showed two echogenic masses in the right atrium and right ventricle. The masses were extended to the pulmonary trunk. Pulmonary artery flow measurements showed the presence of pulmonary and tricuspid obstruction. Surgery was rapidly considered since the baby was hemodynamically unstable. Intraoperative evaluation showed a mass embedded in the interventricular septum that occupy the right ventricular cavity and the right atrium. The tumor involved also the chordae of the tricuspid. Partial resection was done. Tricuspid valve repair was performed by construction of new chordae from the autologous pericardium. The specimen was sent for histopathological analysis. The baby died immediately after surgery. Histological examination of the surgical specimen revealed clear multivacuolated cells filled with lipid droplets and granular intense eosinophilic cytoplasm which confirms the diagnosis of Hibernoma. CONCLUSION: Cardiac Hibernomas are rare benign tumors. The prognosis and treatment strategy is closely dependent on the location, initial clinical presentation and possible complications. The prognosis can be unfavorable if the tumor was obstructive and infiltrate the myocardium.
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spelling pubmed-83403732021-08-06 Neonatal cardiogenic shock revealing obstructive cardiac Hibernoma: case report Gribaa, Rym Kacem, Marwen Ouannes, Sami Majdoub, Wiem Thabet, Houssem Ali, Imen Ben Elheraiche, Aymen Slim, Mehdi Hmissa, Sihem Neffati, Elyes Cherif, Taieb Kortas, Chokri Marah, Jamli Jerbi, Sofiene J Cardiothorac Surg Case Report BACKGROUND: Cardiac Hibernomas are very rare benign tumors and usually remain asymptomatic. Neonatal cardiogenic shock due to cardiac tumors is extremely very rare. Until this date a few cases of cardiac hibernoma have been reported in the literature. Transthoracic echocardiography help in the differential diagnosis, but the definitive diagnosis is histological. The management strategy is not clearly codified. The Aim is to report and discuss the clinical features of a cardiac Hibernoma and review the relevant literature. CASE PRESENTATION: We describe a case of a 2-day-old Caucasian full-term male neonate admitted in neonate intensive care with cardiogenic shock, having fluid resuscitation and inotropic drugs. Ventilatory support was started immediately with the subsequent reestablishment of normal blood pressure. Then he was transferred to the echocardiography laboratory. Transthoracic echocardiography showed two echogenic masses in the right atrium and right ventricle. The masses were extended to the pulmonary trunk. Pulmonary artery flow measurements showed the presence of pulmonary and tricuspid obstruction. Surgery was rapidly considered since the baby was hemodynamically unstable. Intraoperative evaluation showed a mass embedded in the interventricular septum that occupy the right ventricular cavity and the right atrium. The tumor involved also the chordae of the tricuspid. Partial resection was done. Tricuspid valve repair was performed by construction of new chordae from the autologous pericardium. The specimen was sent for histopathological analysis. The baby died immediately after surgery. Histological examination of the surgical specimen revealed clear multivacuolated cells filled with lipid droplets and granular intense eosinophilic cytoplasm which confirms the diagnosis of Hibernoma. CONCLUSION: Cardiac Hibernomas are rare benign tumors. The prognosis and treatment strategy is closely dependent on the location, initial clinical presentation and possible complications. The prognosis can be unfavorable if the tumor was obstructive and infiltrate the myocardium. BioMed Central 2021-08-04 /pmc/articles/PMC8340373/ /pubmed/34348738 http://dx.doi.org/10.1186/s13019-021-01582-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Gribaa, Rym
Kacem, Marwen
Ouannes, Sami
Majdoub, Wiem
Thabet, Houssem
Ali, Imen Ben
Elheraiche, Aymen
Slim, Mehdi
Hmissa, Sihem
Neffati, Elyes
Cherif, Taieb
Kortas, Chokri
Marah, Jamli
Jerbi, Sofiene
Neonatal cardiogenic shock revealing obstructive cardiac Hibernoma: case report
title Neonatal cardiogenic shock revealing obstructive cardiac Hibernoma: case report
title_full Neonatal cardiogenic shock revealing obstructive cardiac Hibernoma: case report
title_fullStr Neonatal cardiogenic shock revealing obstructive cardiac Hibernoma: case report
title_full_unstemmed Neonatal cardiogenic shock revealing obstructive cardiac Hibernoma: case report
title_short Neonatal cardiogenic shock revealing obstructive cardiac Hibernoma: case report
title_sort neonatal cardiogenic shock revealing obstructive cardiac hibernoma: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8340373/
https://www.ncbi.nlm.nih.gov/pubmed/34348738
http://dx.doi.org/10.1186/s13019-021-01582-z
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