首页> 外文期刊>Journal of thoracic imaging >Atypical CT findings of isolated pulmonary Langerhans cell histiocytosis in a 4-year-old boy.
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Atypical CT findings of isolated pulmonary Langerhans cell histiocytosis in a 4-year-old boy.

机译:一个四岁男孩的孤立肺部朗格汉斯细胞组织细胞增生的非典型CT表现。

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A 4-year old boy was admitted to hospital with progressive respiratory failure. A chest roentgenogram revealed hyperinflated lungs and a diffuse reticular pattern. There was no smoking history in the family environment. A thin slice computed tomography of the lungs exhibited extended and diffuse cystic lung disease with no zonal predominance. An open lung biopsy showed pulmonary Langerhans cell histiocytosis. No other organs were involved. Despite treatment initiation the boy succumbed to his pulmonary insufficiency 3 weeks later. Isolated pulmonary Langerhans cell histiocytosis in children may have an unfavorable prognosis and in contrast with adults, it may present on computed tomography with lower lobe predominance and without sparing the lung bases or the anterior parts of middle lobe and lingula.
机译:一名4岁男孩因进行性呼吸衰竭入院。胸部X线照片显示肺部过度充气和弥漫性网状结构。家庭环境中没有吸烟史。肺部的薄层计算机断层扫描显示扩展性和弥漫性囊性肺部疾病,无区域性优势。开放的肺活检显示肺朗格汉斯细胞组织细胞增生。没有其他器官参与。尽管开始治疗,该男孩仍在3周后屈服于肺功能不全。儿童孤立的肺朗格汉斯细胞组织细胞增生症可能预后不良,与成人相反,它可能在计算机体层摄影术中表现出较低的叶优势性,且不保留肺底或中叶和舌前部。

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