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外阴和阴道低度纤维黏液样肉瘤:7 例临床、病理和分子特征及文献复习。

Low-grade Fibromyxoid Sarcoma of the Vulva and Vagina: Clinical, Pathologic, and Molecular Characterization of 7 Cases and Review of the Literature.

机构信息

Division of Women's and Perinatal Pathology.

Department of Pathology, University of North Carolina, Chapel Hill, NC.

出版信息

Am J Surg Pathol. 2022 Sep 1;46(9):1196-1206. doi: 10.1097/PAS.0000000000001906. Epub 2022 Apr 13.

Abstract

Low-grade fibromyxoid sarcoma (LGFMS) is a malignancy with propensity for late relapse that principally affects deep soft tissues of the extremities and trunk. Its occurrence in the lower female genital tract is rare, and thus it may not be always considered in the differential diagnosis. We describe the salient features of 7 vulvovaginal LGFMS identified in the authors' consultation files. Clinical information was obtained from referring pathologists. Archival slides were reviewed, and immunohistochemistry and fluorescence in situ hybridization were performed in cases with available material. Median age was 40 years (range, 34 to 58 y). Primary sites included vulva (n=6) and vagina (n=1). Tumors were 1.2 to 8.7 cm (median, 5.0 cm) in size and grossly circumscribed with firm to focally gelatinous cut surfaces. Microscopically, 5/7 had infiltrative edges. All tumors showed fibrous and myxoid areas, with lobulated myxoid foci in 5/7, comprising storiform, patternless, or (less often) fascicular arrangement of spindled to stellate cells with bland, slender to ovoid nuclei. In all cases, mitoses were <1/2.4 mm 2 , and necrosis was absent. Capillary "arcades" were seen in 3/7. Margins were positive in 3/6. Immunohistochemistry showed positive epithelial membrane antigen in 4/6 and MUC4 in 5/6. Fluorescence in situ hybridization detected FUS rearrangement in 5/7. Both tumors without FUS rearrangement were also negative for EWSR1 rearrangement. All 5 patients with available follow-up were alive and disease-free 10 to 150 months (median, 57 mo) after diagnosis. However, a review of vulvovaginal/pelvic LGFMS previously reported shows recurrences as late as 45 years after initial diagnosis. Pathologists need to be aware that LGFMS can arise in the vulvovaginal region. Tumor lobulation, capillary arcades, and positive MUC4 are helpful features distinguishing LGFMS from other bland myxoid spindle cell neoplasms in the lower female genital tract. Molecular testing can be useful in challenging cases. Complete excision is feasible for most vulvovaginal LGFMS. Long-term surveillance is required as local and/or distant spread can occur decades after diagnosis.

摘要

低度纤维黏液样肉瘤(LGFMS)是一种具有晚期复发倾向的恶性肿瘤,主要影响四肢和躯干的深部软组织。它在女性下生殖道的发生较为罕见,因此在鉴别诊断中可能不常被考虑。我们描述了作者会诊文件中确定的 7 例阴道 LGFMS 的显著特征。临床信息取自转诊病理学家。对有可用材料的病例进行了存档切片复习,并进行了免疫组织化学和荧光原位杂交。中位年龄为 40 岁(范围,34 至 58 岁)。原发部位包括外阴(n=6)和阴道(n=1)。肿瘤大小为 1.2 至 8.7cm(中位数,5.0cm),大体边界清楚,质地坚实至局灶性胶冻样切面。显微镜下,5/7 例肿瘤边缘浸润性。所有肿瘤均显示纤维和黏液样区域,5/7 例肿瘤有分叶状黏液样灶,由梭形至星状细胞呈交织状、模式样或(较少见)束状排列,细胞形态温和,细胞核细长或卵圆形。所有病例的核分裂象均<1/2.4mm2,且无坏死。3/7 例可见毛细血管“拱廊”。3/6 例肿瘤边缘阳性。免疫组织化学显示上皮膜抗原阳性 4/6 例,MUC4 阳性 5/6 例。荧光原位杂交检测到 5/7 例 FUS 重排。无 FUS 重排的 2 例肿瘤也无 EWSR1 重排。5 例有随访资料的患者在诊断后 10 至 150 个月(中位数,57 个月)时均存活且无疾病。然而,对先前报道的阴道/盆腔 LGFMS 的回顾显示,复发时间可晚至初次诊断后 45 年。病理学家需要意识到 LGFMS 可发生在阴道区域。肿瘤分叶、毛细血管拱廊和 MUC4 阳性是将 LGFMS 与女性下生殖道其他良性黏液样梭形细胞肿瘤区分开来的有用特征。分子检测在有挑战性的病例中可能有用。大多数阴道 LGFMS 可行完整切除。由于诊断后几十年可能会出现局部和/或远处播散,因此需要长期随访。

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