临床儿科杂志 ›› 2020, Vol. 38 ›› Issue (8): 612-.doi: 10.3969/j.issn.1000-3606.2020.08.013

• 综合报道 • 上一篇    下一篇

儿童脱屑性间质性肺炎1 例报告并文献复习

郦琳琳, 梁慧, 姚劲, 赵德育, 王全   

  1. 南京医科大学附属儿童医院呼吸科(江苏南京 210008)
  • 出版日期:2020-08-15 发布日期:2020-08-11
  • 通讯作者: 王全 电子信箱:wquan0315@163.com

Desquamative interstitial pneumonia in children: a case report and literature review

 LI Linlin, LIANG Hui, YAO Jin, ZHAO Deyu, WANG Quan   

  1. Department of Respiratory, Children’s Hospital Affiliated to Nanjing Medical University, Nanjing 210008, Jiangsu, China
  • Online:2020-08-15 Published:2020-08-11

摘要: 目的 探讨儿童脱屑性间质性肺炎(DIP)的病因、临床特点、诊治及预后。方法 回顾分析1例按临床-放射病理(C-R-P)模式确诊的DIP患儿的临床资料,并以“desquamative interstitial pneumonia”与“child” 、“ 脱屑性间质性肺炎” 与“儿童”为检索词,在PubMed、万方数据库检索截止至2019年7月的相关文献。结果 4岁男童,咳嗽1个月,伴气促,肺 部中、细湿啰音,杵状指;肺CT示毛玻璃样影和网格影。患儿抗感染治疗临床无好转,行胸腔镜下右肺组织活检术,肺组 织病理符合DIP。随之患儿采用激素治疗,随访44个月,症状消失、病灶基本吸收。文献检索到国内病例11例、国外病例 42例,除外临床资料不完整者,最终筛选获得30例,加上本例患儿共31例,其中男14例、女13例, 4例资料中未提及,年 龄从新生儿~13岁。病因主要为先天性表面活性物质代谢缺陷,其他包括特发性、吸入二手烟、药物以及全身性疾病。临 床表现主要为呼吸困难和干咳,肺部影像学以毛玻璃影为主,肺功能主要为限制性通气障碍。治疗主要采用糖皮质激素和 免疫抑制剂。结论 儿童DIP较为少见,病因和发病机制与成人有显著差别,应尽早肺活检病理检查以确诊,激素和/或免 疫抑制剂为一线治疗药物。

关键词: 脱屑性间质性肺炎; 危险因素; 治疗; 儿童

Abstract: Objective To explore the pathology, clinical manifestation, diagnosis, treatment and prognosis of desquamative interstitial pneumonia (DIP) in children. Methods A child with DIP admitted to Children’s Hospital Affiliated to Nanjing Medical University was analyzed retrospectively. The final diagnosis was made based on the principle of clinicalradiologic-pathologic diagnosis. Related literatures were reviewed. Take “desquamative interstitial pneumonia” and “child” as the search word, 42 cases were retrieved in PubMed until July 2019. Eleven (11) cases in China were retrieved in Wanfang Med Online. 30 cases with complete clinical data and a case in this study were included. The pathological, clinical, and radiological features, lung function, response to treatment and prognosis were summarized. Results A 4-year-old boy presented with chronic cough for 1 month and tachypnea, moist rales and clubbed-fingers. The lung CT showed ground-glass and reticular opacities. After treatment with antibiotics, the condition was not improved. A diagnosis of DIP was confirmed by a thoracoscopic right lung biopsy. The symptoms disappeared after the steroid therapy, and the abnormal findings of chest radiography mostly resolved after 44 months follow-up. A total of 31 cases (14 males and 13 females, gender for 4 cases were not mentioned) were selected into the study with age ranged from newborn to 13 years old. DIP in children is mostly related to an inborn error of surfactant metabolism, and can be idiopathic. Other factors such as secondhand cigarette exposure, drugs as well as systemic disease may be associated with DIP. The main symptoms included dyspnea and dry cough, the chest imaging mostly shows ground glass changes, and pulmonary function tests mainly show a restrictive defect. Main treatments included corticosteroids and immunosuppressive therapy. Conclusions DIP is less frequent with different etiology in children than in adults. Lung biopsy should be performed as early as possible for early diagnosis. DIP is curable to steroid and/or other immunosuppressive drugs.

Key words:  desquamative interstitial pneumonia; risk factors; treatment; child