Koizumi Koji, Abe Emiko, Kusanagi Yasuki, Ito Masaharu
Department of Obstetrics and Gynecology, Ehime University School of Medicine, Ehime, Japan.
J Obstet Gynaecol Res. 2010 Dec;36(6):1252-5. doi: 10.1111/j.1447-0756.2010.01311.x. Epub 2010 Oct 11.
Fetal brain tumors are very rare, and fetal survival is generally poor. Here we present a congenital intracranial immature teratoma, which was prenatally diagnosed. Prenatal ultrasonography and fetal magnetic resonance imaging detected the presence of a massive, heterogeneous intracranial tumor at 26 weeks gestational age. An intracranial tumor lacking normal intracranial structures was detected. The biparietal diameter was 13.1 cm, which is abnormally long. Fetal death occurred at 27 weeks of gestation due to cranial perforation. Postmortem histologic examination revealed the presence of an immature teratoma. Ultrasonography and magnetic resonance imaging are helpful in the prenatal diagnosis and evaluation of intracranial tumors. In conclusion, some cases of giant immature congenital teratoma develop antenatal cranial perforation.
胎儿脑肿瘤非常罕见,胎儿存活率通常很低。在此我们报告一例先天性颅内未成熟畸胎瘤,该病例为产前诊断。产前超声检查和胎儿磁共振成像在孕26周时检测到颅内有一个巨大的、异质性肿瘤。检测到一个缺乏正常颅内结构的颅内肿瘤。双顶径为13.1厘米,异常长。妊娠27周时因颅骨穿孔导致胎儿死亡。尸检组织学检查显示存在未成熟畸胎瘤。超声检查和磁共振成像有助于颅内肿瘤的产前诊断和评估。总之,一些巨大先天性未成熟畸胎瘤病例会发生产前颅骨穿孔。