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Giant placental chorangioma: The first case report in Indonesia

机译:巨大的胎盘Chorangioma:印度尼西亚的第一个案例报告

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摘要

Giant placental chorangioma is a benign non-trophoblastic neoplasm which is rare but often results in serious prenatal complications and adverse pregnancy outcome. Here, we present the first case report of giant placental chorangioma in Indonesia with good clinical outcome, prenatally detected in a 35-year-old G4P2A1 female patient, who presented at 33?weeks of gestation with placenta previa, hemorrhage, anemia, and cardiomegaly. The color Doppler ultrasonography examination showed a large cystic hypoechoic circumscribed intraplacental mass in the parenchymal placenta. The elected caesarian section and mass removal was performed at 36?weeks of gestation. The microscopic appearance of the tumor showed a proliferation of capillary sized vessels with monomorphic endothelial cells. The tumor cells showed immunoreactivity for CD31, CD34, and smooth muscle actin (SMA). The Ki-67labeling index was 30%. Clinical, radiological, histopathological, and immunohistochemical profiles confirmed the diagnosis of giant placental chorangioma.
机译:巨型胎盘性Chorangioma是一种良性的非滋润细胞肿瘤,罕见,但经常导致严重的产前并发症和不良妊娠结果。在这里,我们提出了印度尼西亚巨型胎盘核糖瘤的第一个案例报告,临床结果良好,在35岁的G4P2A1女性患者中预先检测到33岁?妊娠与胎盘,出血,贫血和心脏癌的妊娠。 。彩色多普勒超声检查在实质胎盘中显示出大型囊性低压型颅内鳞状物质。 The elected caesarian section and mass removal was performed at 36?weeks of gestation.肿瘤的显微外观显示毛细管大小的血管含量,具有单体内皮细胞。肿瘤细胞显示CD31,CD34和平滑肌肌动蛋白(SMA)的免疫反应性。 Ki-67标记指数为30%。临床,放射,组织病理学和免疫组织化学型材证实了巨型胎聚板的诊断。

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