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胎儿脑先天性未成熟畸胎瘤。

Congenital immature teratoma of the fetal brain.

作者信息

Rickert C H, Probst-Cousin S, Louwen F, Feldt B, Gullotta F

机构信息

Institut für Neuropathologie, Westfälische Wilhelms-Universität, Münster, Germany.

出版信息

Childs Nerv Syst. 1997 Oct;13(10):556-9. doi: 10.1007/s003810050137.

Abstract

Congenital intracranial tumors are very rare and only account for 0.5-1.5% of all childhood brain tumors. Even rarer are those with prenatal manifestation. The most common of these present at birth are teratomas, which show divergent differentiation with 90% of them containing tissues from all three germ layers. We report a rare case of an intrauterine congenital immature teratoma in a female fetus at 23 weeks of gestation, which was sonographically diagnosed in vivo by detection of the tumor and associated craniomegaly. Because of the poor prognosis, termination of the pregnancy was induced by Rivanol instillation. The cerebral tumor was confirmed at autopsy and was not associated with any other malformations. Histological and immunohistochemical features of this tumor are presented.

摘要

先天性颅内肿瘤非常罕见,仅占所有儿童脑肿瘤的0.5 - 1.5%。产前表现的肿瘤更为罕见。出生时最常见的此类肿瘤是畸胎瘤,其具有分化差异,其中90%包含来自所有三个胚层的组织。我们报告一例罕见的宫内先天性未成熟畸胎瘤病例,该病例为一名妊娠23周的女性胎儿,通过超声检查在体内检测到肿瘤及相关的巨头症而得以诊断。由于预后不良,通过羊膜腔内注入利凡诺引产。尸检证实了脑部肿瘤,且未发现任何其他畸形。本文展示了该肿瘤的组织学和免疫组化特征。

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