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Long-Term Survival after Wide Resection of Malignant Fibrous Histiocytoma of the Chest Wall

机译:广泛切除胸壁恶性纤维组织细胞瘤后的长期生存

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摘要

Primary malignant fibrous histiocytoma (MFH) of the chest wall is extremely rare and is characterized by aggressive features, including a high incidence of local recurrence and distant metastasis. Surgical resection of the chest wall is the primary modality of management. However, surgical treatment is not generally recommended in patients with evidence of distant metastasis. Here, we present a case of chest wall MFH along with a schwannoma mimicking distant metastasis in the right upper arm. The patient was treated by radical en bloc resection and survived for more than 9 years without recurrence.
机译:胸壁原发性恶性纤维组织细胞瘤(MFH)极为罕见,其特征是侵袭性特征,包括局部复发和远处转移的高发率。胸壁的外科切除是处理的主要方式。但是,对于有远处转移迹象的患者,一般不建议手术治疗。在这里,我们介绍一例胸壁MFH以及一个模仿右上臂远处转移的神经鞘瘤。该患者接受了根治性全切除术治疗,存活了9年以上而未复发。

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