低体重婴儿先天性肺叶气肿的左上肺叶切除术

Left Upper Lobectomy for Congenital Lobar Emphysema in a Low Weight Infant.

作者信息

Kanakis Meletios, Petsios Konstantinos, Bobos Dimitrios, Sarafidis Kosmas, Nikopoulos Stefanos, Kyriakoulis Konstantinos, Lioulias Achilleas, Giannopoulos Nicholas

机构信息

Department of Pediatric and Congenital Heart Surgery, Onassis Cardiac Surgery Center, Athens, 17674 Kallithea, Greece.

Department of Neonatology and Neonatal Intensive Care Unit, Aristotle University of Thessaloniki, Hippokration Hospital, 54642 Thessaloniki, Greece.

出版信息

Case Rep Surg. 2016;2016:4182741. doi: 10.1155/2016/4182741. Epub 2016 Aug 15.

DOI:10.1155/2016/4182741

PMID:27597924

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5002461/

Abstract

Congenital lobar emphysema (CLE) is a rare lung congenital malformation. Differential diagnosis of the disease remains challenging in an infant with acute respiratory distress. We report a case of a 3-week-old female infant with a weight of 2.1 kg who presented respiratory distress related to CLE. Left upper lobectomy was performed and she had an uneventful recovery.

摘要

先天性大叶性肺气肿（CLE）是一种罕见的肺先天性畸形。对于患有急性呼吸窘迫的婴儿，该疾病的鉴别诊断仍然具有挑战性。我们报告一例3周龄、体重2.1千克的女婴，其因先天性大叶性肺气肿出现呼吸窘迫。实施了左上肺叶切除术，她恢复顺利。