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婴儿并存肺内型和肺外型隔离症的外科治疗

Surgical treatment of coexisting intra and extralobar sequestration in an infant.

作者信息

Saleh Ahmad, Awwad Adam, Bhattacharyya Ratul, Bhattacharyya Nishith

机构信息

School of Medicine, St. George's University, True Blue, Grenada, West Indies.

Department of Surgery, St. Joseph's University Medical Center, Patterson, NJ 07503, United States.

出版信息

J Surg Case Rep. 2024 Oct 17;2024(10):rjae660. doi: 10.1093/jscr/rjae660. eCollection 2024 Oct.

Abstract

Pulmonary sequestration is a rare congenital malformation in which a nonfunctional segment of lung tissue has no communication with the tracheobronchial tree and does not participate in gas exchange. We present a rare case of a 20-month old female with extralobar pulmonary sequestration that was diagnosed at birth. The patient was also found to have a coexisting intralobar sequestration, found during surgery.

摘要

肺隔离症是一种罕见的先天性畸形,其中肺组织的无功能节段与气管支气管树没有连通,不参与气体交换。我们报告一例罕见病例,一名20个月大的女性,出生时被诊断为叶外型肺隔离症。在手术过程中还发现该患者并存叶内型肺隔离症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca67/11486683/977306306de1/rjae660f1.jpg

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