42岁男性,进行性呼吸困难,肿块迅速增大

Jinesh P. Mehta, Juan Guardiola
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引用次数: 1

摘要

恶性纤维组织细胞瘤(MFH),又称未分化高级别多形性肉瘤,占美国所有软组织肉瘤的20-24%。发病率高峰出现在五、六十岁,男女比例为2:1。MFH通常见于四肢软组织,累及肺是罕见的。我们报告一例胸膜MFH患者以前胸膜肺结核,他有一个肺叶切除术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A 42-year-old man with progressive dyspnea and a rapidly growing mass

Malignant fibrous histiocytoma (MFH), also known as undifferentiated high grade pleomorphic sarcoma, accounts for 20–24% of all soft tissue sarcomas in the US. Peak incidence is in the fifth and sixth decades of life, with a 2:1 male to female distribution. MFH is usually seen in the soft tissues of the extremity and involvement of the lung is rare. We report a case of pleural MFH in a patient with previous pleuro-pulmonary tuberculosis for which he had a lobectomy.

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