Thoracoscopic Plication for Neonatal Diaphragmatic Eventration With Intrathoracic Ectopic Kidney: A Rare Case Report

Coexistence of congenital diaphragmatic eventration (CDE) and an intrathoracic ectopic kidney (ITEK) is extremely rare and may lead to substantial respiratory distress in neonates. This study reports the case of a small-for-gestational-age male neonate presenting with respiratory distress and requiring nasal continuous positive airway pressure. Computed tomography revealed right-sided CDE accompanied by an ITEK. At 44 days old, the infant underwent thoracoscopic diaphragmatic plication. CO<sub>2</sub> insufflation during surgery led to spontaneous reduction of the ectopic kidney into the abdominal cavity, eliminating the need for direct manipulation. The postoperative course was uneventful, and at 14 months, the child remains healthy with no signs of recurrence. This case demonstrates that thoracoscopic plication is a safe and effective option for managing this rare condition, even in low-birth-weight infants. It also suggests that the ectopic position of the kidney is a secondary consequence of diaphragmatic laxity.

Authors

Institutions

Publication Details

Journal
Asian Journal of Endoscopic Surgery
Published
2025-01-01
DOI
https://doi.org/10.1111/ases.70157
Primary Topic
Congenital Diaphragmatic Hernia Studies
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Thoracoscopic Plication for Neonatal Diaphragmatic Eventration With Intrathoracic Ectopic Kidney: A Rare Case Report

Eunyoung Jung
Asian Journal of Endoscopic Surgery
Congenital Diaphragmatic Hernia Studies
article

Thoracoscopic Plication for Neonatal Diaphragmatic Eventration With Intrathoracic Ectopic Kidney: A Rare Case Report

Eunyoung Jung
article en

Abstract

Coexistence of congenital diaphragmatic eventration (CDE) and an intrathoracic ectopic kidney (ITEK) is extremely rare and may lead to substantial respiratory distress in neonates. This study reports the case of a small-for-gestational-age male neonate presenting with respiratory distress and requiring nasal continuous positive airway pressure. Computed tomography revealed right-sided CDE accompanied by an ITEK. At 44 days old, the infant underwent thoracoscopic diaphragmatic plication. CO<sub>2</sub> insufflation during surgery led to spontaneous reduction of the ectopic kidney into the abdominal cavity, eliminating the need for direct manipulation. The postoperative course was uneventful, and at 14 months, the child remains healthy with no signs of recurrence. This case demonstrates that thoracoscopic plication is a safe and effective option for managing this rare condition, even in low-birth-weight infants. It also suggests that the ectopic position of the kidney is a secondary consequence of diaphragmatic laxity.

Asian Journal of Endoscopic SurgeryVol. 18(1)
Keimyung University Dongsan Medical Center (KR), Keimyung University (KR)
Openalex Percentile: Top 57%
Congenital Diaphragmatic Hernia Studies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.