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Multimodal radiology diagnostics for recurrent congenital diaphragmatic hernia in a child with congenital heart disease: clinical case

https://doi.org/10.24884/1682-6655-2024-23-1-76-80

Abstract

Congenital diaphragmatic hernia (CDH) is a severe congenital malformation that occurs as a result of delayed closure of the pleuroperitoneal canal or the diaphragm failure, which leads to the displacement of abdominal organs into the thoracic cavity. Timely diagnosis of recurrent diaphragmatic hernia in the long-term period causes great difficulties. The article presents a clinical observation of a 1-year-and-8-months old female patient operated on for false congenital diaphragmatic hernia and congenital heart defect during the newborn period. Chest X-ray at the outpatient stage allowed diagnosing a relapse of CDH and determining the urgency of hospitalization. In the hospital, the diagnosis was confirmed by computed tomography, surgical treatment was performed.

About the Authors

M. K. Shapina
Children’s City Polyclinic № 68
Russian Federation

Shapina Maiia K. – Radiologist, SOGAZ Multidisciplinary Medical Centre, Head, Radiology Department

20/1, Nastanovnikov str., Saint Petersburg, 195426



N. A. Ilyina
North-Western State Medical University named after I. I. Mechnikov ; Children’s Сity Multidisciplinary Clinical Specialized Center of High Medical Technologies
Russian Federation

Ilyina Natalia A. – MD, Professor, Radiology Department

47, Piskarevskii str., Saint Petersburg, 195067

14, Avangardnaya str., Saint Petersburg, 198205



M. I. Gurova
Children’s City Polyclinic № 68
Russian Federation

Gurova Maria I. – High-Category Pediatrician, Candidate of Medical Sciences (PhD), Head, Outpatient Department

20/1, Nastanovnikov str., Saint Petersburg, 195426



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For citations:


Shapina M.K., Ilyina N.A., Gurova M.I. Multimodal radiology diagnostics for recurrent congenital diaphragmatic hernia in a child with congenital heart disease: clinical case. Regional blood circulation and microcirculation. 2024;23(1):76-80. (In Russ.) https://doi.org/10.24884/1682-6655-2024-23-1-76-80

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ISSN 1682-6655 (Print)
ISSN 2712-9756 (Online)