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首页> 外文期刊>The Internet Journal of Surgery >Which Should Be Considered For The Clear Surgical Margin Of Postradiation Malignant Fibrous Histiocytoma: Tumor-Free Or Radiation-Free Margin?
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Which Should Be Considered For The Clear Surgical Margin Of Postradiation Malignant Fibrous Histiocytoma: Tumor-Free Or Radiation-Free Margin?

机译:放射后恶性纤维组织细胞瘤的明确手术切缘应考虑哪些因素:无肿瘤或无辐射的切缘?

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Malignant fibrous histiocytoma is one of the most common soft tissue sarcomas originating from extremities. Its presentation after radiation, especially in chest wall, is a very rare event. The prognosis is poor due to its aggressiveness and local recurrence rate is high. Its main treatment is surgical excision. The presented case describes postradiation malignant fibrous histiocytoma treated with repetitive extensive resection and reconstruction of the chest wall in a patient diagnosed with breast cancer ten years ago with long survival. We suggest that patients who undergo wide excision with negative margins (radiation-free) have long survival. Introduction Malignant fibrous histiocytoma (MFH) is one of the most common soft tissue sarcomas arising from differentiation of fibroblasts and histiocytes (1). Firstly, it was defined by O'Brien and Stout in 1964. The incidence in middle and advanced ages is high. Its most common locations are extremities (70%) and retroperitoneal space (12-14%) (1,2). MFH in the chest wall is a very rare entity, especially in patients previously treated with radiation for breast cancer, and it is rarely reported in the literature (3). Restricted surgery is not recommended for the treatment of MFH of the chest wall, because of the high incidence of local recurrence and distant metastasis. The main recommended treatment is aggressive radical surgery performed after diagnosis (4). The rationale of this article is to discuss the aggressive surgical treatment of postradiation MFH of the chest wall with long survival and to review the related literature. Case A forty-one-year-old woman was hospitalized for a mass of the left anterior chest wall. She had undergone left modified radical mastectomy for infiltrative ductal carcinoma 10 years before. The disease stage was T1NM0 and estrogen, progesterone receptors and c erb B2 expression were negative. She had antracyclin based chemotherapy and radiation therapy in the postoperative period at a dosage of 40 Gray (Gy). She was in remission without any problem during the past 10 years of survey. Six months ago, she was admitted because of a 7cm mass located at the mastectomy incision. A limited excision was performed. The pathological examination revealed a MFH. Three months later she was referred to our institution because of tumor relapse reaching a diameter of 5cm within 10 days. We performed a large excision of the tumor, including the major and minor pectoral muscles with intact surgical margins (tumor free). The defect was reconstructed with a split thickness skin graft. Two months later, she was rehospitalized because of a rapidly growing mass with a diameter of 10 cm in its largest dimension. The ulcerated, hemorrhagic and stinking mass, restricting the abduction of the arm and rotations, was determined on the left chest wall. It was surpassing the clavicula, coming down to the level of the sixth rib, 3cm away from the sternum at the medial margin. Laterally, it invaded the left forearm, medially it reached the posterior axillary line (Figure 1). Magnetic resonance examination of the thorax revealed a mass of 7x9x11cm in the upper part of left hemithorax. There was no metastasis to the other parts of the body or invasion to the chest detected. Extensive surgery was planned for the removal of the mass. The patient had been informed and she accepted the operation. The clavicula was excised; the left subclavian artery and vein were tied and cut. Together with the scapula, the left arm, the former grafted location and the tumor tissue was excised completely (a flap containing the lateral surface of the arm from deltoid muscle to tumor-free area has been prepared). The part exposed to radiation was excised together with the tumor with a surgical margin (histopathologically verified) of 4cm (Figure 2). There was no invasion on ribs. The defect was restored with a deltoid flap (Figure 3). In the postoperative period, chemotherapy has been planned for the patie
机译:恶性纤维组织细胞瘤是起源于四肢的最常见的软组织肉瘤之一。放射后,特别是在胸壁,其出现非常罕见。由于其侵略性,预后差,局部复发率高。其主要治疗方法是手术切除。本病例描述了十年前被确诊患有乳腺癌且具有长生存期的患者,经反复广泛切除和胸壁重建治疗的放射后恶性纤维组织细胞瘤。我们建议接受广泛切除而切缘阴性(无放射)的患者生存期较长。简介恶性纤维组织细胞瘤(MFH)是由成纤维细胞和组织细胞分化引起的最常见的软组织肉瘤之一(1)。首先,它是由O'Brien和Stout在1964年定义的。中老年人的发病率很高。它最常见的位置是四肢(70%)和腹膜后间隙(12-14%)(1,2)。胸壁的MFH是非常罕见的实体,尤其是在先前接受过放射线治疗的乳腺癌患者中,这在文献中很少报道(3)。由于局部复发和远处转移的发生率高,不建议使用限制性手术治疗胸壁MFH。建议的主要治疗方法是在诊断后进行积极的根治性手术(4)。本文的目的是讨论具有长生存期的胸壁放射后MFH的积极外科治疗方法,并复习相关文献。病例一名四十一岁妇女因左前胸壁肿块住院。 10年前,她因浸润性导管癌接受了左改良根治性乳房切除术。疾病分期为T1NM0,雌激素,孕激素受体和Cerb B2表达均为阴性。术后以40 Gray(Gy)的剂量进行了基于环霉素的化疗和放疗。在过去的十年调查中,她的病情没有任何问题。六个月前,她因乳房切除术切口处7厘米的肿块而入院。进行了有限的切除。病理检查发现MFH。三个月后,她因肿瘤复发在10天内达到5厘米的直径而被转介到我们的机构。我们对肿瘤进行了大范围切除,包括具有完整手术切缘(无肿瘤)的主要和次要的胸肌。用厚薄的皮肤移植物重建缺损。两个月后,由于体重迅速增加,最大直径为10厘米,她被送进了医院。在左胸壁确定了溃疡,出血和发臭的肿块,限制了手臂的外展和旋转。它超过了锁骨,下降到第六肋骨的水平,距内侧边缘距胸骨3cm。在侧面,它侵入了左前臂,在内侧到达后腋线(图1)。胸部的磁共振检查显示左半胸腔上部有7x9x11cm的肿块。没有发现转移到身体的其他部位,也没有发现侵袭到胸部。已计划进行大手术以切除肿块。病人已被告知,她接受了手术。锁骨被切除;左锁骨下动脉和静脉被捆扎并切断。连同肩cap骨一起,将左臂,前一个移植位置和肿瘤组织完全切除(已准备好一个皮瓣,其中包含臂的从三角肌到无肿瘤区域的侧面)。将暴露于放射线的部分与肿瘤一起切除,手术切缘(组织病理学证实)为4cm(图2)。肋骨没有受到侵袭。用三角肌皮瓣修复缺损(图3)。在术后阶段,已计划对患者进行化疗

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