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. ShapinaRussian Federation
Shapina Maiia K. – Radiologist, SOGAZ Multidisciplinary Medical Centre, Head, Radiology Department
20/1, Nastanovnikov str., Saint Petersburg, 195426
N. A. Ilyina
Russian Federation
Ilyina Natalia A. – MD, Professor, Radiology Department
47, Piskarevskii str., Saint Petersburg, 195067
14, Avangardnaya str., Saint Petersburg, 198205
M. I. Gurova
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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Review
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