Foregut Duplication Cysts in a Patient With Congenital Diaphragmatic Hernia: A Case Report
Aleksandra I Sadecka, Zaneta Slowik-Moczydlowska
TL;DR
A newborn was diagnosed with a rare combination of congenital diaphragmatic hernia and multiple esophageal duplication cysts.
Contribution
This case report highlights the rare co-occurrence of congenital diaphragmatic hernia and multiple esophageal duplication cysts.
Findings
The patient had congenital diaphragmatic hernia and multiple esophageal duplication cysts.
This combination is a rare clinical scenario with potential for complex management.
Abstract
Esophageal duplication cysts are a rare form of foregut developmental abnormality with heterogeneous manifestations due to their variable location and size. Congenital diaphragmatic hernia is a congenital defect resulting from incomplete diaphragm formation, with a wide spectrum of severity. It is typically diagnosed antenatally and managed surgically in the neonatal period. We present a case report of a newborn with a rare co-occurrence of congenital diaphragmatic hernia and multiple esophageal duplication cysts.
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Taxonomy
TopicsCongenital Diaphragmatic Hernia Studies · Gastrointestinal disorders and treatments · Superconducting Materials and Applications