An Infant With Interstitial Lung Disease of Rare Cause

被引：5

作者：

Li, Cong ^{[1
]}

Zhang, Huishan ^{[1
]}

Mo, Jiali ^{[1
]}

Wang, Yanqiong ^{[5
]}

Song, Danyu ^{[1
]}

Wu, Penghui ^{[1
]}

Xiong, Yan ^{[2
]}

Qiu, Jianxing ^{[3
]}

Wang, Guangfa ^{[4
]}

Ye, Leping ^{[1
]}

机构：

[1] Peking Univ First Hosp, Dept Pediat, Beijing, Peoples R China

[2] Peking Univ First Hosp, Dept Pathol, Beijing, Peoples R China

[3] Peking Univ First Hosp, Dept Radiol, Beijing, Peoples R China

[4] Peking Univ First Hosp, Dept Resp & Crit Care Med, Beijing, Peoples R China

[5] Zhengzhou Univ, Childrens Hosp, Dept Pediat Resp Med, Zhengzhou, Peoples R China

来源：

CHEST | 2022年 / 161卷 / 05期

基金：

中国国家自然科学基金;

关键词：

CRYOBIOPSY; DIAGNOSIS;

D O I：

10.1016/j.chest.2021.12.639

中图分类号：

R4 [临床医学];

学科分类号：

1002 ; 100602 ;

摘要：

CASE PRESENTATION: An 11-month-old boy was admitted to our hospital because of "recurrent cough with intermittent dyspnea for more than 8 months, aggravated for 1 month." The baby began experiencing a recurrent milk-choking problem within 1.5 months after birth. He had been hospitalized four times, but the symptoms recurred. One month previously, the symptoms were aggravated and a chest CT scan performed at outside hospital showed interstitial changes. Pediatric bronchoscopy revealed bronchial inflammatory features, with hemosiderin-laden macrophages being found in BAL fluid (BALF). Also, periodic acid-Schiff (PAS) staining showed positive results, which indicated the possibility of pulmonary alveolar proteinosis (PAP) or idiopathic pulmonary hemosiderosis (IPH).

引用

页码：E273 / E278

页数：6

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