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一例罕见病因所致间质性肺病婴儿。

An Infant With Interstitial Lung Disease of Rare Cause.

机构信息

Department of Pediatrics, Peking University First Hospital, Beijing, China.

Department of Pediatrics, Peking University First Hospital, Beijing, China; Department of Pediatric Respiratory Medicine, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou, China.

出版信息

Chest. 2022 May;161(5):e273-e278. doi: 10.1016/j.chest.2021.12.639.

DOI:10.1016/j.chest.2021.12.639
PMID:35526896
Abstract

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).

摘要

一名 11 个月大的男婴因“反复咳嗽伴间歇性呼吸困难 8 个月余,加重 1 个月”入院。患儿生后 1.5 月即开始反复出现呛奶问题,曾住院 4 次,但症状反复发作。1 个月前症状加重,外院胸部 CT 显示间质性改变。儿科支气管镜检查显示支气管炎症特征,支气管肺泡灌洗液(BALF)中可见含铁血黄素的巨噬细胞。过碘酸雪夫(PAS)染色阳性,提示肺肺泡蛋白沉积症(PAP)或特发性肺含铁血黄素沉着症(IPH)可能。

相似文献

1
An Infant With Interstitial Lung Disease of Rare Cause.一例罕见病因所致间质性肺病婴儿。
Chest. 2022 May;161(5):e273-e278. doi: 10.1016/j.chest.2021.12.639.
2
Autoimmune pulmonary alveolar proteinosis and idiopathic pulmonary haemosiderosis: a dual pathology.自身免疫性肺肺泡蛋白沉积症和特发性肺含铁血黄素沉着症:双重病理学。
BMJ Case Rep. 2021 Apr 2;14(4):e241048. doi: 10.1136/bcr-2020-241048.
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Pulmonary alveolar proteinosis: a case report.肺泡蛋白沉积症:一例报告
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Autoimmune pulmonary alveolar proteinosis developed during immunosuppressive treatment in polymyositis with interstitial lung disease: a case report.自身免疫性肺泡蛋白沉积症在多发性肌炎伴间质性肺病的免疫抑制治疗中发生:一例报告。
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Therapeutic limited bronchoalveolar lavage with fiberoptic bronchoscopy as a bridging procedure prior to total lung lavage in a patient with pulmonary alveolar proteinosis: a case report.肺泡蛋白沉积症患者在全肺灌洗前采用纤维支气管镜进行治疗性有限支气管肺泡灌洗作为桥接程序:一例报告
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J Clin Immunol. 2025 Feb 4;45(1):71. doi: 10.1007/s10875-025-01861-7.
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A rare cause of immune dysregulation, prolidase deficiency: a case report and review of the literature.免疫失调的罕见病因——脯氨酰二肽酶缺乏症:一例报告并文献复习
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Utility of Transbronchial Cryobiopsy via Flexible Bronchoscope in Diagnosis of Isolated Pulmonary LCH: A Case Report.
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