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http://dx.doi.org/10.4103/0019-5049.170041 | DOI Listing |
Int J Emerg Med
October 2024
, Addis Ababa, Ethiopia.
Cureus
July 2024
2nd Pediatric Surgery Department, Panagiotis & Aglaia Kyriakou Childrens' Hospital, Athens, GRC.
Morgagni hernia (MH), also known as a retrosternal or parasternal hernia, is a rare type of congenital diaphragmatic hernia (CDH) characterized by a defect in the anterior diaphragm. Patients with late-diagnosed MH typically present with vague gastrointestinal or respiratory symptoms. In some instances, MH is incidentally identified through chest X-rays performed for other reasons, such as foreign body ingestion, as illustrated in our presented case.
View Article and Find Full Text PDFJACC Case Rep
July 2024
Minneapolis Heart Institute-Abbott Northwestern Hospital, Minneapolis, Minnesota, USA.
A 40-year-old male presented with an inferior ST-segment elevation myocardial infarction. Multimodality imaging identified a ventricular septal defect and a right ventricular free wall dissection. He was bridged with a percutaneous microaxial left ventricular assist device to successful surgical repair.
View Article and Find Full Text PDFEur J Case Rep Intern Med
May 2024
Internal Medicine, Shifa College of Medicine, Islamabad, Pakistan.
Introduction: Ventricular septal defect (VSD) is a severe complication following acute myocardial infarction (MI) resulting from mechanical disruption of the interventricular septum due to extensive myocardial necrosis. Despite advances in management, the mortality rate approaches 50%. We report a case of a 58-year-old male with VSD following MI who was successfully treated with a delayed surgical approach after haemodynamic support using Impella.
View Article and Find Full Text PDFCase Rep Pediatr
May 2024
UF Department of Pediatrics, 4740 NW 39th PI B, Gainesville, FL 32606, USA.
Congenital diaphragmatic hernia (CDH) is a rare anomaly resulting from incomplete closure of pleuroperitoneal canals during fetal development, often presenting with acute respiratory distress in neonates. This case report highlights a 17-year-old female with recurrent episodes of acute left upper quadrant (LUQ) pain and no history of trauma or dietary change. A computerized tomography (CT) scan taken during her second presentation to the emergency department led to a diagnosis of left-sided CDH.
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