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一例产前诊断的原始神经外胚层肿瘤病例。

A prenatal diagnosed case of primitive neuroectodermal tumor.

作者信息

Sahin Figen Kir, Koken Gulengul, Cosar Emine, Koken Resit, Sahin Onder, Gokden Murat

机构信息

Department of Obstetrics and Gynecology, Afyonkarahisar Kocatepe University, Faculty of Medicine, Afyon, Turkey.

出版信息

Fetal Diagn Ther. 2008;23(4):267-70. doi: 10.1159/000123613. Epub 2008 Apr 14.

Abstract

Congenital brain tumors presenting in the first year of life account for 1.4-8.5% of all childhood brain tumors. Only 18% of congenital brain tumors are diagnosed before or at delivery. Primitive neuroectodermal tumor (PNET) is a highly malignant, small, blue-cell tumor which is characterized by early recurrence, metastasis, and high mortality. It makes up 13% of all fetal and neonatal brain tumors. Prenatal diagnosis of PNET or other congenital brain tumors is important because the presence of tumors may alter the time and mode of delivery and postnatal care planning. A prenatal case of PNET is described that was diagnosed with ultrasonography and magnetic resonance imaging; the case was confirmed histopathologically at postmortem examination.

摘要

出生后第一年出现的先天性脑肿瘤占所有儿童脑肿瘤的1.4 - 8.5%。只有18%的先天性脑肿瘤在分娩前或分娩时被诊断出来。原始神经外胚层肿瘤(PNET)是一种高度恶性的小蓝细胞瘤,其特点是早期复发、转移和高死亡率。它占所有胎儿和新生儿脑肿瘤的13%。PNET或其他先天性脑肿瘤的产前诊断很重要,因为肿瘤的存在可能会改变分娩时间和方式以及产后护理计划。本文描述了一例通过超声检查和磁共振成像诊断出的产前PNET病例;该病例在尸检时经组织病理学证实。

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