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年轻患者中表现为β-hCG 升高的多形性未分化子宫肉瘤伴良性平滑肌瘤罕见变异:病例报告及文献复习。

Pleomorphic Undifferentiated Uterine Sarcoma in a Young Patient Presenting With Elevated Beta-hCG and Rare Variants of Benign Leiomyoma: A Case Report and Review of the Literature.

机构信息

Departments of Pathology (V.K., K.R.) Gynecology Oncology (P.S., D.P.), Hospital network of the University of Montreal (CHUM), Montreal, Quebec, Canada.

出版信息

Int J Gynecol Pathol. 2020 Jul;39(4):362-366. doi: 10.1097/PGP.0000000000000606.

Abstract

Leiomyosarcoma (LMS) is a malignant mesenchymal neoplasm showing smooth muscle differentiation. Uterine LMS is more frequent that nonuterine LMS, and represents 1% of all malignant neoplasms of the uterus. Pleomorphic undifferentiated uterine sarcoma is a rare entity, and is defined by high-grade sarcoma histology with loss of muscular markers. Several cases of pleomorphic undifferentiated uterine sarcoma have been reported in the literature, with worse clinical outcome when compared with conventional LMS. Here we report the first case of a pleomorphic undifferentiated uterine sarcoma in association with LMS in a 33 yr old woman. The patient presented clinically with recurrent vaginal bleeding and suspicion of a trophoblastic tumor. Ancillary testing revealed moderately elevated beta-hCG (49.7 U/L) and no metastatic disease on imaging. Gross examination of the hysterectomy specimen revealed a large heterogenous necrotic uterine mass infiltrating <50% of the myometrium. Microscopic evaluation showed pleomorphic undifferentiated uterine sarcoma adjacent to a nodule of leiomyoma with bizarre nuclei, with loss of myogenic markers in the high grade component. Other findings included a foci of conventional LMS, and diffuse uterine leiomyomatosis. Although beta-hCG dropped to normal levels during follow-up, the patient developed metastatic lesions to the lung at 6 mo postop. Initial elevation of beta-hCG may have correlated with the aggressive histology of the tumor, as reported by some groups previously. Recognition of pleomorphic undifferentiated uterine sarcoma and its distinction from conventional LMS is essential for patient prognosis and management.

摘要

平滑肌肉瘤(LMS)是一种具有平滑肌分化特征的恶性间叶性肿瘤。子宫 LMS 比非子宫 LMS 更常见,占子宫所有恶性肿瘤的 1%。多形性未分化子宫肉瘤是一种罕见的实体瘤,其特征为高级别肉瘤组织学表现伴有肌源性标志物的丧失。文献中已有几例多形性未分化子宫肉瘤的报道,与传统的 LMS 相比,其临床结局更差。在此,我们报告首例多形性未分化子宫肉瘤合并 LMS 的病例,患者为 33 岁女性,临床表现为反复阴道出血,且疑似滋养细胞肿瘤。辅助检查显示β-HCG 中度升高(49.7 U/L),影像学未见转移病灶。子宫切除术标本大体检查显示一个大的异质性坏死性子宫肿块,浸润肌层<50%。显微镜下评估显示多形性未分化子宫肉瘤紧邻具有奇异核的平滑肌瘤结节,高级别成分中肌源性标志物缺失。其他发现包括常规 LMS 病灶和弥漫性子宫平滑肌瘤病。尽管在随访过程中β-HCG 降至正常水平,但患者在术后 6 个月时出现肺转移病灶。β-HCG 的最初升高可能与肿瘤的侵袭性组织学有关,如一些研究小组之前报道的那样。识别多形性未分化子宫肉瘤及其与传统 LMS 的区别对患者的预后和管理至关重要。

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