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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4697253PMC
http://dx.doi.org/10.4103/0019-5049.170041DOI Listing

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Article Synopsis
  • Congenital diaphragmatic hernia (CDH) is a rare birth defect where abdominal organs move into the chest cavity through a diaphragmatic defect, leading to respiratory issues, commonly diagnosed in newborns but can also appear later in life.
  • A case involving a 2-year-old boy from Ethiopia presented with respiratory distress, initially misdiagnosed as tension pneumothorax based on chest x-ray, but further imaging revealed CDH with abdominal organs compressing the lung.
  • The case highlights the need for careful diagnosis in respiratory distress cases, as misinterpretation of imaging can lead to inappropriate treatments; accurate diagnosis through advanced imaging is vital for effective management and recovery.
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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.

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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.

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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.

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Beyond the Neonate: A Delayed Presentation of Congenital Diaphragmatic Hernia in a 17-Year-Old.

Case 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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