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复杂先天性畸形:一名11个月大男童左肺发育不全、左肺动脉缺如及先天性心脏病的病例报告

Complex Congenital Anomalies: A Case Report of Left Pulmonary Hypoplasia, Absent Left Pulmonary Artery, and Congenital Heart Disease in an 11-Month-Old Male Child.

作者信息

Reddy Naramreddy Sudheesh, Varma Ashish, Vagha Keta, Raut Vaibhav, Javvaji Chaitanya Kumar, Manchineni Sai Bhavani, Kommareddy Anirudh, Vagha Jayant D, Murhekar Siddhartha

机构信息

Pediatrics, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.

Cardiology, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.

出版信息

Cureus. 2024 Jun 28;16(6):e63430. doi: 10.7759/cureus.63430. eCollection 2024 Jun.

DOI:10.7759/cureus.63430
PMID:39077294
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11284345/
Abstract

A rare disorder called pulmonary hypoplasia is characterized by inadequate lung development, which frequently results in respiratory dysfunction and other related abnormalities. We present a case of an 11-month-old male child with left lung hypoplasia, absent left pulmonary artery, and ventricular septal defect (VSD). The child exhibited symptoms of cough and cold, with a history of recurrent respiratory tract infections since birth. Cardiovascular examination revealed a pan systolic murmur consistent with VSD, while respiratory examination indicated decreased air entry on the left side. Imaging studies confirmed the absence of the left pulmonary artery and left lung hypoplasia. Despite recommendations for VSD surgery, the child's parents declined surgical intervention, leading to discharge against medical advice. This case highlights the challenges in managing pulmonary hypoplasia, especially when accompanied by complex congenital heart defects, and underscores the importance of multidisciplinary care and parental involvement in decision-making.

摘要

一种名为肺发育不全的罕见疾病,其特征是肺部发育不足,这常常导致呼吸功能障碍及其他相关异常。我们报告一例11个月大的男童,患有左肺发育不全、左肺动脉缺如和室间隔缺损(VSD)。该患儿表现出咳嗽和感冒症状,自出生以来有反复呼吸道感染史。心血管检查发现全收缩期杂音,与室间隔缺损相符,而呼吸检查显示左侧呼吸音减弱。影像学研究证实左肺动脉缺如及左肺发育不全。尽管建议进行室间隔缺损手术,但患儿家长拒绝手术干预,导致其自行出院。本病例凸显了管理肺发育不全的挑战,尤其是伴有复杂先天性心脏缺陷时,并强调了多学科护理及家长参与决策的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e72/11284345/79ad370c959c/cureus-0016-00000063430-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e72/11284345/992c5b35e51a/cureus-0016-00000063430-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e72/11284345/f40480d4f43d/cureus-0016-00000063430-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e72/11284345/79ad370c959c/cureus-0016-00000063430-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e72/11284345/992c5b35e51a/cureus-0016-00000063430-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e72/11284345/f40480d4f43d/cureus-0016-00000063430-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e72/11284345/79ad370c959c/cureus-0016-00000063430-i03.jpg

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本文引用的文献

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Congenital pulmonary hypoplasia combined with congenital cardiac disease and ectopic kidney: a case report.先天性肺发育不全合并先天性心脏病及异位肾:一例报告
Asian Biomed (Res Rev News). 2023 Oct 26;17(5):244-248. doi: 10.2478/abm-2023-0066. eCollection 2023 Oct.
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Infant with Clinical Evidence of Pulmonary Hypoplasia: A Case Report.患有肺发育不全临床证据的婴儿:一例报告
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