Zhou Ping, Wang Weiya, Fu Yiyun, Zhang Ying, Liang Zuoyu, Tang Yuan, Jiang Lili
Department of Pathology, West China Hospital, Sichuan University, Chengdu, China.
Front Pediatr. 2022 Apr 7;10:836276. doi: 10.3389/fped.2022.836276. eCollection 2022.
Persistent pulmonary interstitial emphysema (PPIE) is known to be related to mechanical ventilation and preterm. However, PPIE is also reported rarely in non-ventilated and full-term infants. Its relationship with respiratory infection is rarely reported in the literature. PPIE is difficult to diagnose and always mimics other congenital thoracic malformations (CTMs), such as congenital cystic adenomatoid malformation (CCAM).
The objective of this study was to evaluate clinicopathological and radiographic features of PPIE with respiratory infection and to detect the possible infectious pathogens.
From January 2011 to December 2019, six cases were confirmed pathologically with PPIE from a large cohort of 477 resected CTMs in West China Hospital of Sichuan University. Clinical and radiographic features were obtained from patients' medical records and follow-up. The present study aimed to analyze clinicopathological and radiographic features and to detect the infectious pathogens by metagenomic next-generation sequencing (mNGS).
The six PPIE cases included four girls and two boys, ranging from 2 months to 5 years; 100% (5/5) of the available cases were full-term and without mechanical ventilation. CCAM were suspected in 66.7% (4/6) patients; 66.7% (4/6) cases affected a single lobe, and 33.3% (2/6) cases affected both lung lobes. Clinically, all six PPIEs were presented with symptoms of respiratory infection and diagnosed with pneumonia. All six patients were treated by surgery after anti-infective treatment. The pathologic characteristics showed lung cysts with variable size along the bronchovascular bundles, the cysts had a discontinuous fibrotic wall with a smooth inner surface lined with uninucleated and/or multinucleated macrophages. was detected in patient No. 1. Human beta-herpesvirus 5 was detected in patient No. 2. , and were detected in patient No. 5, and no infectious pathogen was detected in 50% (3/6, No. 3, No. 4, and No. 6) of cases.
Six rare cases of PPIE with respiratory infection were treated by surgery after anti-infective treatment. All five available cases were full-term infants without mechanical ventilation. The histological characteristics of PPIE were the wall of cysts composed of a thin layer of discontinuous fibrous tissue and lined with uninucleated or/and multinucleated macrophages.
持续性肺间质肺气肿(PPIE)已知与机械通气和早产有关。然而,非通气足月婴儿中也鲜有PPIE的报道。其与呼吸道感染的关系在文献中也很少被提及。PPIE难以诊断,且常与其他先天性胸廓畸形(CTM)相似,如先天性囊性腺瘤样畸形(CCAM)。
本研究旨在评估合并呼吸道感染的PPIE的临床病理和影像学特征,并检测可能的感染病原体。
2011年1月至2019年12月,从四川大学华西医院477例接受手术切除的CTM大样本队列中,病理确诊6例PPIE。从患者病历和随访中获取临床和影像学特征。本研究旨在分析临床病理和影像学特征,并通过宏基因组下一代测序(mNGS)检测感染病原体。
6例PPIE患者中,4例为女孩,2例为男孩,年龄2个月至5岁;100%(5/5)的可用病例为足月且无机械通气。66.7%(4/6)的患者曾怀疑患有CCAM;66.7%(4/6)的病例累及单个肺叶,33.3%(2/6)的病例累及两个肺叶。临床上,所有6例PPIE均表现为呼吸道感染症状并被诊断为肺炎。所有6例患者在抗感染治疗后均接受了手术治疗。病理特征显示沿支气管血管束有大小不一的肺囊肿,囊肿壁为不连续的纤维组织,内表面光滑,衬有单核和/或多核巨噬细胞。1号患者检测到[未提及具体病原体名称]。2号患者检测到人类β疱疹病毒5。5号患者检测到[未提及具体病原体名称],50%(3/6,3号、4号和6号患者)的病例未检测到感染病原体。
6例合并呼吸道感染的罕见PPIE病例在抗感染治疗后接受了手术治疗。所有5例可用病例均为无机械通气的足月婴儿。PPIE的组织学特征是囊肿壁由一层薄的不连续纤维组织构成,内衬单核或/和多核巨噬细胞。