A Rare Case of Neonatal Desmoid Tumor Leading to Severe Aortic Coarctation: Review of Literature and Case Report

Desmoid tumors are a rare entity, especially in the pediatric population. There are no reports of such a tumor in newborns. They are associated with high rates of morbidity and mortality, even though they are benign soft tissue tumors. This is due to them exhibiting locally aggressive growth with th...

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Main Authors: Irina Maria Margarint, Tammam Youssef, Cristina Filip, Ana-Mihaela Bizubac, Alexandru Popescu, Iulian Rotaru, Olguta Untaru, Stefan Manolache, Vlad Anton Iliescu, Radu Vladareanu
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Language:English
Published: MDPI AG 2025-01-01
Series:Life
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Online Access:https://www.mdpi.com/2075-1729/15/1/123
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author Irina Maria Margarint
Tammam Youssef
Cristina Filip
Ana-Mihaela Bizubac
Alexandru Popescu
Iulian Rotaru
Olguta Untaru
Stefan Manolache
Vlad Anton Iliescu
Radu Vladareanu
author_facet Irina Maria Margarint
Tammam Youssef
Cristina Filip
Ana-Mihaela Bizubac
Alexandru Popescu
Iulian Rotaru
Olguta Untaru
Stefan Manolache
Vlad Anton Iliescu
Radu Vladareanu
author_sort Irina Maria Margarint
collection DOAJ
description Desmoid tumors are a rare entity, especially in the pediatric population. There are no reports of such a tumor in newborns. They are associated with high rates of morbidity and mortality, even though they are benign soft tissue tumors. This is due to them exhibiting locally aggressive growth with the compression or invasion of adjacent structures. Abdominal localization is most commonly reported, although there are reports of mediastinal desmoid tumors. We present the case of a 6-day male patient with a mediastinal desmoid tumor that led to severe aortic coarctation with hemodynamic instability. The tumor also compressed the left pulmonary artery and obstructed the left main bronchus. The initial management consisted of successful emergency surgery with partial resection of the tumor mass and coarctation repair. In the postoperative setting, the patient evolved with severe respiratory dysfunction which was managed with tracheostomy, allowing weaning the child from the mechanical ventilation one month after surgery, along with chemotherapy. We also review the literature, focusing on the management of desmoid tumors.
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id doaj-art-09ce2028bdf645198cb055ddaa4631a3
institution Kabale University
issn 2075-1729
language English
publishDate 2025-01-01
publisher MDPI AG
record_format Article
series Life
spelling doaj-art-09ce2028bdf645198cb055ddaa4631a32025-01-24T13:38:53ZengMDPI AGLife2075-17292025-01-0115112310.3390/life15010123A Rare Case of Neonatal Desmoid Tumor Leading to Severe Aortic Coarctation: Review of Literature and Case ReportIrina Maria Margarint0Tammam Youssef1Cristina Filip2Ana-Mihaela Bizubac3Alexandru Popescu4Iulian Rotaru5Olguta Untaru6Stefan Manolache7Vlad Anton Iliescu8Radu Vladareanu9Faculty of Medicine, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, RomaniaDepartment of Cardiac Surgery, Emergency Clinical Hospital for Children “Maria Skłodowska Curie”, 077120 Bucharest, RomaniaFaculty of Medicine, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, Romania“Marie S. Curie Children’s Emergency Hospital” Bucharest, Neonatal Intensive Care Unit, 20 Constantin Brancoveanu Street, District 4, 041451 Bucharest, RomaniaDepartment of Cardiac Surgery, Emergency Clinical Hospital for Children “Maria Skłodowska Curie”, 077120 Bucharest, RomaniaDepartment of Cardiac Surgery, Emergency Clinical Hospital for Children “Maria Skłodowska Curie”, 077120 Bucharest, RomaniaDepartment of Cardiac Surgery, Emergency Clinical Hospital for Children “Maria Skłodowska Curie”, 077120 Bucharest, Romania“Marie S. Curie Children’s Emergency Hospital” Bucharest, Neonatal Intensive Care Unit, 20 Constantin Brancoveanu Street, District 4, 041451 Bucharest, RomaniaFaculty of Medicine, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, RomaniaFaculty of Medicine, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, RomaniaDesmoid tumors are a rare entity, especially in the pediatric population. There are no reports of such a tumor in newborns. They are associated with high rates of morbidity and mortality, even though they are benign soft tissue tumors. This is due to them exhibiting locally aggressive growth with the compression or invasion of adjacent structures. Abdominal localization is most commonly reported, although there are reports of mediastinal desmoid tumors. We present the case of a 6-day male patient with a mediastinal desmoid tumor that led to severe aortic coarctation with hemodynamic instability. The tumor also compressed the left pulmonary artery and obstructed the left main bronchus. The initial management consisted of successful emergency surgery with partial resection of the tumor mass and coarctation repair. In the postoperative setting, the patient evolved with severe respiratory dysfunction which was managed with tracheostomy, allowing weaning the child from the mechanical ventilation one month after surgery, along with chemotherapy. We also review the literature, focusing on the management of desmoid tumors.https://www.mdpi.com/2075-1729/15/1/123desmoid tumoraortic coarctationnewbornrespiratory failure
spellingShingle Irina Maria Margarint
Tammam Youssef
Cristina Filip
Ana-Mihaela Bizubac
Alexandru Popescu
Iulian Rotaru
Olguta Untaru
Stefan Manolache
Vlad Anton Iliescu
Radu Vladareanu
A Rare Case of Neonatal Desmoid Tumor Leading to Severe Aortic Coarctation: Review of Literature and Case Report
Life
desmoid tumor
aortic coarctation
newborn
respiratory failure
title A Rare Case of Neonatal Desmoid Tumor Leading to Severe Aortic Coarctation: Review of Literature and Case Report
title_full A Rare Case of Neonatal Desmoid Tumor Leading to Severe Aortic Coarctation: Review of Literature and Case Report
title_fullStr A Rare Case of Neonatal Desmoid Tumor Leading to Severe Aortic Coarctation: Review of Literature and Case Report
title_full_unstemmed A Rare Case of Neonatal Desmoid Tumor Leading to Severe Aortic Coarctation: Review of Literature and Case Report
title_short A Rare Case of Neonatal Desmoid Tumor Leading to Severe Aortic Coarctation: Review of Literature and Case Report
title_sort rare case of neonatal desmoid tumor leading to severe aortic coarctation review of literature and case report
topic desmoid tumor
aortic coarctation
newborn
respiratory failure
url https://www.mdpi.com/2075-1729/15/1/123
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