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黏液纤维肉瘤。75例临床病理分析,重点关注低级别变异型。

Myxofibrosarcoma. Clinicopathologic analysis of 75 cases with emphasis on the low-grade variant.

作者信息

Mentzel T, Calonje E, Wadden C, Camplejohn R S, Beham A, Smith M A, Fletcher C D

机构信息

Soft Tissue Tumour Unit, St. Thomas's Hospital, London, England.

出版信息

Am J Surg Pathol. 1996 Apr;20(4):391-405. doi: 10.1097/00000478-199604000-00001.

Abstract

Myxofibrosarcoma is one of the most common sarcomas in the extremities of elderly patients. We analysed the clinicopathologic features in a series of 75 patients. All patients were adults (range, 22-91 years; median, 66 years) with an approximately equal incidence in men and women. Thirty-five tumors arose in the lower and 25 in the upper extremities, nine on the trunk, two each in the retroperitoneum and the head and neck region, and one each in the pelvis and penis. Forty-eight cases (69.5%) were located in dermal or subcutaneous tissues. Distinctive histologic features included the following: a commonly nodular growth pattern; a myxoid matrix containing elongated, curvilinear capillaries; and fusiform, round or stellate tumor cells with indistinct cell margins, slightly eosinophilic cytoplasm, and hyperchromatic atypical nuclei. These lesions varied from a hypocellular, mainly myxoid, and purely spindle-cell appearance (low-grade neoplasms) to high-grade, pleomorphic (malignant fibrous histiocytoma-like) lesions with multinucleated giant cells, high mitotic activity, and areas of necrosis. Immunohistochemistry in 44 cases revealed only vimentin and occasional actin positivity. Ultrastructurally, tumor cells had a fibroblastic phenotype. DNA flow cytometry and proliferation analysis showed an association between aneuploidy and histologic grade. An average follow-up of 45 months (range, 5-300 months) in 60 cases has revealed local recurrence in 33 cases (54%). Thirteen patients developed metastases, and 13 tumor-related deaths occurred. A short interval to first local recurrence was associated with poor clinical outcome. The rate of local recurrence was independent of histologic grade, but only intermediate and high-grade neoplasms metastasized. The depth of the primary lesion did not influence the incidence of local recurrence. However, in deep-seated neoplasms, the incidence of metastases was higher and the percentage of tumor-related deaths was twice as high as in superficially located lesions, reflecting the fact that deep-seated lesions tended to be higher-grade, larger tumors. Myxofibrosarcoma tends to become progressively higher grade in recurrences, as demonstrated in five cases in our series. The poorly recognized low-grade myxofibrosarcoma is emphasized, as proper diagnosis and treatment and scrupulous follow-up are mandatory to avoid local recurrence and gradual tumor progression to a higher-grade neoplasm that may then metastasize.

摘要

黏液纤维肉瘤是老年患者四肢最常见的肉瘤之一。我们分析了75例患者的临床病理特征。所有患者均为成年人(年龄范围22 - 91岁;中位年龄66岁),男女发病率大致相等。35个肿瘤发生于下肢,25个发生于上肢,9个位于躯干,2个分别位于腹膜后以及头颈部区域,1个位于骨盆,1个位于阴茎。48例(69.5%)位于真皮或皮下组织。独特的组织学特征如下:常见结节状生长模式;含有细长、曲线形毛细血管的黏液样基质;梭形、圆形或星状肿瘤细胞,细胞边界不清,胞质轻度嗜酸性,核深染且异型。这些病变从细胞稀少、主要为黏液样且纯粹为梭形细胞外观(低级别肿瘤)到高级别、多形性(恶性纤维组织细胞瘤样)病变不等,后者伴有多核巨细胞、高有丝分裂活性及坏死区域。44例患者的免疫组化显示仅波形蛋白阳性,偶尔肌动蛋白阳性。超微结构上,肿瘤细胞具有成纤维细胞表型。DNA流式细胞术和增殖分析显示非整倍体与组织学分级相关。60例患者平均随访45个月(范围5 - 300个月),33例(54%)出现局部复发。13例患者发生转移,13例患者死于肿瘤相关疾病。首次局部复发间隔时间短与临床预后不良相关。局部复发率与组织学分级无关,但仅中级和高级别肿瘤发生转移。原发病变深度不影响局部复发发生率。然而,在深部肿瘤中,转移发生率更高,肿瘤相关死亡百分比是浅表病变的两倍,这反映出深部病变往往是级别更高、体积更大的肿瘤。如我们系列中的5例所示,黏液纤维肉瘤复发时往往级别逐渐升高。强调了认识不足的低级别黏液纤维肉瘤,因为正确的诊断、治疗及严格的随访对于避免局部复发以及肿瘤逐渐进展为可能发生转移的高级别肿瘤是必不可少的。

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