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Prenatal management of diaphragmatic rhabdomyosarcoma presenting with fetal hydrops.

机译:产前管理膈横纹肌肉瘤与易漏诊。

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摘要

Fetal malignant tumors are rare. We present a case of intrauterine diagnosis of a diaphragmatic tumor presenting with fetal hydrops at 32 weeks' gestation. The sonographic findings were bilateral pleural effusion, ascites and skin edema. A large right-sided diaphragmatic tumor was identified. Owing to the findings on ultrasound and magnetic resonance imaging a solid malignant tumor was suspected. The pleural effusions were drained and malignant cells identified. Because of rapid tumor progression Cesarean section was performed and a hydropic female newborn was delivered at 34 + 0 weeks' gestation. There was no sign of metastatic disease. Postnatally tumor biopsy revealed an alveolar rhabdomyosarcoma. Therapy included chemotherapy and secondary surgical intervention. After a good primary response with complete remission after 6 months, the rhabdomyosarcoma relapsed at 12 months with cerebral metastasis. The prognosis was poor. Copyright ? 2012 ISUOG. Published by John Wiley & Sons, Ltd.
机译:胎儿的恶性肿瘤是罕见的。宫内诊断膈在32周的胎儿肿瘤出现水肿妊娠。双边胸腔积液、腹水和皮肤水肿。被确认。超声和磁共振成像固体恶性肿瘤被怀疑。积液是排水和恶性细胞识别。剖腹产了,浮肿的女性新生儿34 + 0周交货妊娠。疾病。肺泡横纹肌肉瘤。化疗和二次手术治疗。后一个好主反应完全6个月后缓解,横纹肌肉瘤在12个月内复发脑转移。预后较差。由约翰·威利出版& Sons,有限公司

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