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

IF 0.9 Q4 ORTHOPEDICS
Eunyoung Jung
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引用次数: 0

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. CO2 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.

Abstract Image

胸腔镜应用于新生儿横膈膜膨出合并胸内异位肾:罕见病例报告。
先天性膈膨出(CDE)和胸内异位肾(ITEK)共存是极其罕见的,可能导致新生儿严重的呼吸窘迫。本研究报告的情况下,小胎龄男性新生儿表现为呼吸窘迫和需要鼻腔持续气道正压。计算机断层扫描显示右侧CDE伴ITEK。44天大时,婴儿接受胸腔镜下横膈膜应用。手术过程中CO2的充气导致异位肾自动减少到腹腔,消除了直接操作的需要。术后过程顺利,14个月时,孩子保持健康,无复发迹象。该病例表明,胸腔镜应用是治疗这种罕见疾病的安全有效的选择,即使是低出生体重婴儿。这也提示肾脏的异位是膈肌松弛的继发后果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.00
自引率
10.00%
发文量
129
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