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An Infant With Interstitial Lung Disease of Rare Cause.
Li, Cong; Zhang, Huishan; Mo, Jiali; Wang, Yanqiong; Song, Danyu; Wu, Penghui; Xiong, Yan; Qiu, Jianxing; Wang, Guangfa; Ye, Leping.
Afiliación
  • Li C; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Zhang H; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Mo J; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Wang Y; Department of Pediatrics, Peking University First Hospital, Beijing, China; Department of Pediatric Respiratory Medicine, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou, China.
  • Song D; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Wu P; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Xiong Y; Department of Pathology, Peking University First Hospital, Beijing, China.
  • Qiu J; Department of Radiology, Peking University First Hospital, Beijing, China.
  • Wang G; Department of Respiratory and Critical Care Medicine, Peking University First Hospital, Beijing, China.
  • Ye L; Department of Pediatrics, Peking University First Hospital, Beijing, China. Electronic address: yeleping@bjmu.edu.cn.
Chest ; 161(5): e273-e278, 2022 05.
Article en En | MEDLINE | ID: mdl-35526896
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).
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteinosis Alveolar Pulmonar / Enfermedades Pulmonares Intersticiales / Hemosiderosis / Enfermedades Pulmonares Tipo de estudio: Diagnostic_studies Límite: Child / Humans / Infant / Male Idioma: En Revista: Chest Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteinosis Alveolar Pulmonar / Enfermedades Pulmonares Intersticiales / Hemosiderosis / Enfermedades Pulmonares Tipo de estudio: Diagnostic_studies Límite: Child / Humans / Infant / Male Idioma: En Revista: Chest Año: 2022 Tipo del documento: Article País de afiliación: China