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Successful surgical treatment of a 1160 g neonate with cardiac teratoma and severe foetal hydrops: a case report
BACKGROUND: Prenatally diagnosed pericardial teratoma present a rare finding with an unfavourable prognosis due to frequently associated Foetal hydrops and limited treatment options. We report a successful surgical resection of a prenatally diagnosed cardiac teratoma in a 1160 g neonate with severe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954248/ https://www.ncbi.nlm.nih.gov/pubmed/33738399 http://dx.doi.org/10.1093/ehjcr/ytaa527 |
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author | Beichl, Matthias Thanhaeuser, Margarita Ulm, Barbara Zimpfer, Daniel |
author_facet | Beichl, Matthias Thanhaeuser, Margarita Ulm, Barbara Zimpfer, Daniel |
author_sort | Beichl, Matthias |
collection | PubMed |
description | BACKGROUND: Prenatally diagnosed pericardial teratoma present a rare finding with an unfavourable prognosis due to frequently associated Foetal hydrops and limited treatment options. We report a successful surgical resection of a prenatally diagnosed cardiac teratoma in a 1160 g neonate with severe Foetal hydrops and cardiac deterioration. CASE SUMMARY: The patient was transferred in utero to our institution due to prior diagnosed pericardial mass and severe foetal hydrops, which necessitated caesarean section one day after arrival at a gestational age of 28 + 0 weeks. After intubation, the patient was stabilized by surgical drainage of 60 mL of pericardial effusion. Further clinical worsening of the patient on the day of life 12 demanded urgent intervention, so that in toto resection of the tumour was performed at a bodyweight of 1160 g. Histopathological analysis revealed a teratoma and the patient is in excellent clinical condition one year after surgery. DISCUSSION: This case report demonstrates that an interdisciplinary, two-staged approach can be a feasible and promising treatment option in patients with prenatally diagnosed teratoma and severe Foetal hydrops in a critical circulatory state. Furthermore, it illustrated that resection of pericardial masses can be successfully performed at a bodyweight as low as 1160 g. |
format | Online Article Text |
id | pubmed-7954248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-79542482021-03-17 Successful surgical treatment of a 1160 g neonate with cardiac teratoma and severe foetal hydrops: a case report Beichl, Matthias Thanhaeuser, Margarita Ulm, Barbara Zimpfer, Daniel Eur Heart J Case Rep Case Report BACKGROUND: Prenatally diagnosed pericardial teratoma present a rare finding with an unfavourable prognosis due to frequently associated Foetal hydrops and limited treatment options. We report a successful surgical resection of a prenatally diagnosed cardiac teratoma in a 1160 g neonate with severe Foetal hydrops and cardiac deterioration. CASE SUMMARY: The patient was transferred in utero to our institution due to prior diagnosed pericardial mass and severe foetal hydrops, which necessitated caesarean section one day after arrival at a gestational age of 28 + 0 weeks. After intubation, the patient was stabilized by surgical drainage of 60 mL of pericardial effusion. Further clinical worsening of the patient on the day of life 12 demanded urgent intervention, so that in toto resection of the tumour was performed at a bodyweight of 1160 g. Histopathological analysis revealed a teratoma and the patient is in excellent clinical condition one year after surgery. DISCUSSION: This case report demonstrates that an interdisciplinary, two-staged approach can be a feasible and promising treatment option in patients with prenatally diagnosed teratoma and severe Foetal hydrops in a critical circulatory state. Furthermore, it illustrated that resection of pericardial masses can be successfully performed at a bodyweight as low as 1160 g. Oxford University Press 2021-01-04 /pmc/articles/PMC7954248/ /pubmed/33738399 http://dx.doi.org/10.1093/ehjcr/ytaa527 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the European Society of Cardiology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Case Report Beichl, Matthias Thanhaeuser, Margarita Ulm, Barbara Zimpfer, Daniel Successful surgical treatment of a 1160 g neonate with cardiac teratoma and severe foetal hydrops: a case report |
title | Successful surgical treatment of a 1160 g neonate with cardiac teratoma and severe foetal hydrops: a case report |
title_full | Successful surgical treatment of a 1160 g neonate with cardiac teratoma and severe foetal hydrops: a case report |
title_fullStr | Successful surgical treatment of a 1160 g neonate with cardiac teratoma and severe foetal hydrops: a case report |
title_full_unstemmed | Successful surgical treatment of a 1160 g neonate with cardiac teratoma and severe foetal hydrops: a case report |
title_short | Successful surgical treatment of a 1160 g neonate with cardiac teratoma and severe foetal hydrops: a case report |
title_sort | successful surgical treatment of a 1160 g neonate with cardiac teratoma and severe foetal hydrops: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954248/ https://www.ncbi.nlm.nih.gov/pubmed/33738399 http://dx.doi.org/10.1093/ehjcr/ytaa527 |
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