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卵巢原发性平滑肌肉瘤:偶发的罕见恶性肿瘤。

Primary leiomyosarcoma of ovary: A rare malignancy as an incidental finding.

机构信息

Department of Pathology, ESIC Medical College, Faridabad, Haryana, India.

Department of Gynecology, ESIC Medical College, Faridabad, Haryana, India.

出版信息

Indian J Pathol Microbiol. 2022 Oct-Dec;65(4):938-941. doi: 10.4103/ijpm.ijpm_99_21.

Abstract

Primary leiomyosarcoma (PLMS) of the ovary is extremely rare tumors comprising 1% of ovarian tumors. About 3% of all ovarian malignancies are primary ovarian sarcomas. Only 72 cases have been reported till date. A 57-year-old postmenopausal female presented with abdominal pain for the last 6 months. Ultrasonography and MRI revealed a heterogeneously enhancing solid lobulated mass in the left adnexa abutting the fundus of the uterus and bowel loops. The endometrial cavity was normal. Ovarian markers CA 125, CEA, CA 19.9, and all hematological parameters were within normal limits. LDH was near normal (284 IU/ml). The specimen was sent for frozen section and a diagnosis of malignant spindle cell lesion of ovary was rendered. Histopathology of the ovarian mass revealed intersecting fascicles of tumor cells consisting of ovoid to spindle-shaped cells having a moderate amount of cytoplasm. Bizarre and atypical cells were seen singly dispersed and in small aggregates along with the brisk mitotic activity. Focal areas of necrosis and hemorrhage were also noted. Immunohistochemistry showed strong positivity for smooth muscle actin and Caldesmon while focal positivity for Desmin and Epithelial Membrane Antigen (EMA) was noted. The lesion was negative for Inhibin, Calretinin, and CD 117 and S100. The final diagnosis of primary ovarian Leiomyosarcoma was given based on histopathology and Immunohistochemistry. PLMS of the ovary are rare incidental findings in postmenopausal women. These are highly malignant tumors and carry a poor prognosis. Hence, early diagnosis and surgical treatment with cytoreduction improve patient survival.

摘要

原发性卵巢平滑肌肉瘤(PLMS)是一种非常罕见的肿瘤,占卵巢肿瘤的 1%。约 3%的卵巢恶性肿瘤为原发性卵巢肉瘤。迄今为止,仅报告了 72 例。一位 57 岁绝经后女性因腹痛就诊,已持续 6 个月。超声和 MRI 显示左侧附件内有不均匀强化的实性分叶状肿块,与子宫底部和肠袢相邻。子宫内膜腔正常。卵巢标志物 CA 125、CEA、CA 19.9 和所有血液学参数均在正常范围内。LDH 接近正常(284IU/ml)。标本送检行冰冻切片,诊断为卵巢恶性梭形细胞瘤。卵巢肿块的组织病理学显示肿瘤细胞的交织束,由卵圆形至梭形细胞组成,具有中等量的细胞质。可见单个分散的奇异和非典型细胞,以及少量聚集的细胞,伴有活跃的有丝分裂。还注意到局灶性坏死和出血。免疫组织化学显示平滑肌肌动蛋白和钙调蛋白强阳性,而结蛋白和上皮膜抗原(EMA)呈局灶阳性。该病变对抑制素、钙结合蛋白和 CD117 和 S100 呈阴性。根据组织病理学和免疫组织化学检查,最终诊断为原发性卵巢平滑肌肉瘤。绝经后妇女中偶然发现的卵巢 PLMS 非常罕见。这些是高度恶性肿瘤,预后不良。因此,早期诊断和以细胞减灭术为主的手术治疗可提高患者生存率。

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