以复发性气胸为表现的肺囊性纤维组织细胞瘤1例。

Christos Kakos, Savvas Lampridis, Georgios Geropoulos, Reena Khiroya, Achilleas Antonopoulos, Sofoklis Mitsos, Nikolaos Panagiotopoulos
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引用次数: 0

摘要

肺囊性纤维组织细胞瘤是一种非常罕见的病理实体,它既可以作为原发性肺肿瘤,也可以作为皮肤病变的转移灶,称为细胞纤维组织细胞瘤。在此,我们提出的情况下,19岁的男子复发性气胸谁是手术管理,并最终被诊断为肺囊性纤维组织细胞瘤。临床医生应将此病纳入肺囊性病变的鉴别诊断,并注意其与细胞纤维组织细胞瘤的关系。报告更多的病例是必要的,以进一步阐明疾病的自然过程并优化其管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cystic fibrohistiocytic tumour of the lung presenting with recurrent pneumothoraces: a case report.

Cystic fibrohistiocytic tumour of the lung is a very rare pathological entity that occurs either as a primary pulmonary neoplasm or as a metastasis from skin lesions called cellular fibrous histiocytomas. Herein, we present the case of a 19-year old man with a history of recurrent pneumothoraces who was managed surgically and was eventually diagnosed with cystic fibrohistiocytic tumour of the lung. Clinicians should include this disease in the differential diagnosis of pulmonary cystic lesions and be aware of its association with cellular fibrous histiocytoma. Reporting of more cases is warranted to further elucidate the natural course of the disease and optimise its management.

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