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Cystic Lung Disease in a Young man

机译:年轻人患有囊性肺疾病

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A 32-year-old man was admitted in the Emergency Department with acute dyspnea secondary to spontaneous pneumothorax. He had history of spontaneous pneumothorax 2 years ago.He was active cigarette smoker (10 pack/year). The family history was unremarkable for lung diseases. Additionally, he had no systemic complaints.The lung HRCT revealed multiple bizarre-shaped cysts distributed in both lungs with more severe involvement of upper and middle parts (Figure 1).Since the HRCT findings were characteristic and he was smoker, the diagnosis of pulmonary langerhans cell histiocytosis (PLCH) was proposed. Small chest tube was inserted in left side and after 5 days it was easily removed.He was recommended to quit smoking and close follow-up.
机译:一名32岁的男子因急诊呼吸道疾病而继发于自发性气胸,被送入急诊室。他2年前有自发性气胸病史,他是活跃的吸烟者(10包/年)。家族病史对肺部疾病影响不大。此外,他没有系统性的不适。肺HRCT显示在双肺中分布有多个奇形异状的囊肿,上部和中部受累更为严重(图1)。由于HRCT的发现具有特征性且是吸烟者,因此可诊断为肺提出了朗格汉斯细胞组织细胞增生症(PLCH)。将小胸管插入左侧,五天后很容易取出,建议他戒烟并密切随访。

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