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Desmoid Tumors of the Chest Wall

机译:胸壁皮样肿瘤

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摘要

Chest wall desmoid tumors (DT) are rare pathologic entities with microscopic features similar to, or undistinguishable from, fibromas or fibrosarcomas. From 1996 to 2001, four patients with DT were surgically managed in our department. Their ages ranged from 27 years to 43 years (mean 32.25 years, median 29.5 years), A resection of the lesion was performed with negative margins of 4 cm around the tumor (wide resection). A reconstruction of the chest wall was also performed with polytetrafiuoroethylene (PTFE) in 2 patients and methylmethacrolate with Marlex mesh in 1 patient One patient had a recurrence 15 months later, and was admitted for complementary resection, and remains disease-free for 5 years. The rest 3 patients are disease-free for 6 months to 5 years Resection must include all adjacent, overlying and underlying musculature as well as soft tissues and any spare skin from the procedure should be used Prognosis after a wide resection is good.
机译:胸壁皮肤样瘤(DT)是罕见的病理学实体,其微观特征与纤维瘤或纤维肉瘤相似或不可区分。从1996年到2001年,我科手术治疗了4例DT。他们的年龄从27岁到43岁(平均32.25岁,中位数29.5岁)不等,对病灶进行切除,肿瘤周围有4 cm的负切缘(广泛切除)。还对2例患者进行了聚四氟乙烯(PTFE)重建胸壁的重建,对1例患者进行了Marlex网状的甲基丙烯酸甲酯的重建。1例患者在15个月后复发,并接受了辅助切除术,并保持了5年无病。其余3例患者在6个月至5年内无病,切除必须包括所有相邻的,上覆的和下层的肌肉组织以及软组织,并且应使用该过程中剩余的皮肤进行大范围切除后的预后良好。

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