巨大胎盘绒毛管瘤:印度尼西亚首例病例报告

Q4 Medicine
Emilia Theresia , Detty Siti Nurdiati , Irianiwati Widodo
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引用次数: 6

摘要

巨大胎盘脉管瘤是一种罕见的良性非滋养细胞肿瘤,但常导致严重的产前并发症和不良的妊娠结局。在此,我们报告了印度尼西亚首例临床结果良好的巨大胎盘脉管瘤病例报告,该病例产前发现于一名35岁的G4P2A1女性患者,她在妊娠33周时出现了前胎盘、出血、贫血和心脏肥大。彩色多普勒超声检查显示实质胎盘内有一个大的囊性低回声围界肿块。在妊娠36周时选择剖宫产并切除肿块。肿瘤镜下可见毛细血管大小增生,内皮细胞呈单一形态。肿瘤细胞对CD31、CD34和平滑肌肌动蛋白(SMA)表现出免疫反应性。ki -67标记指数为30%。临床,放射学,组织病理学和免疫组织化学分析证实了巨大胎盘脉管瘤的诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Giant placental chorangioma: The first case report in Indonesia

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.

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来源期刊
Human Pathology: Case Reports
Human Pathology: Case Reports Medicine-Pathology and Forensic Medicine
CiteScore
0.50
自引率
0.00%
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审稿时长
16 weeks
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