A 10-month-old infant with respiratory distress and hypoxemia

D. Hughes
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Abstract

 A 10-month-old infant with Prader-Willi Syndrome presented with a 7 month history of increased work of breathing, wheeze, inspiratory crepitations, and mild hypoxemia. Subsequent investigations including chest CT suggested the diagnosis to be neuroendocrine cell hyperplasia of infancy (NEHI). NEHI is a rare cause of children’s interstitial lung disease. Childhood interstitial lung disease should be considered in an infant with persistent tachypnea, crepitations, and hypoxemia.
一个10个月大的婴儿出现呼吸窘迫和低氧血症
一例10个月大的普瑞德-威利综合征婴儿,有7个月的呼吸功增加、喘息、吸气性心悸和轻度低氧血症病史。随后的检查包括胸部CT显示诊断为婴儿神经内分泌细胞增生(NEHI)。NEHI是儿童间质性肺疾病的罕见病因。儿童间质性肺疾病应考虑在婴儿持续呼吸急促,心悸,和低氧血症。
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