Korostyshevskaya Alexandra, Gornostaeva Alyona, Volkov Rem, Yarnykh Vasily
Institute "International Tomography Center" of the Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation.
Novosibirsk State Medical University, Novosibirsk, Russian Federation.
Radiol Case Rep. 2020 Nov 19;16(1):201-204. doi: 10.1016/j.radcr.2020.11.003. eCollection 2021 Jan.
Iniencephaly (IE) is a rare neural tube malformation involving severe head retroflexion and deformity of the spine. IE is typically accompanied with other congenital abnormalities and carrying a poor fetal prognosis. This report presents radiological findings in a rare case of IE associated with multiple malformations of the skull, spine, face, heart, and body. A 44-year-old pregnant female underwent an obstetric ultrasound examination on the 26th week of gestation followed by fetal magnetic resonance imaging on the 36th week. Imaging revealed complex developmental anomalies, which led to the diagnosis of IE with a large cervical meningocele, occipital bone defect, spina bifida of the cervical vertebrae, multiple malformed vertebra, deformed face, coarctation of the aortic arch, and hypoplastic lungs. Based on these findings, a decision to terminate pregnancy was made. Pathological examination of the fetus showed close agreement with imaging. The presented case underscores the importance of multimodal imaging for clinical decision making in the management of complex neural tube malformations.
无脑畸形(IE)是一种罕见的神经管畸形,包括严重的头部后屈和脊柱畸形。IE通常伴有其他先天性异常,胎儿预后不良。本报告介绍了一例罕见的IE病例的影像学表现,该病例伴有颅骨、脊柱、面部、心脏和身体的多种畸形。一名44岁的孕妇在妊娠26周时接受了产科超声检查,随后在36周时进行了胎儿磁共振成像。影像学检查发现了复杂的发育异常,诊断为IE合并巨大颈膨出、枕骨缺损、颈椎脊柱裂、多个畸形椎体、面部畸形、主动脉弓缩窄和肺发育不全。基于这些发现,决定终止妊娠。胎儿的病理检查结果与影像学检查结果高度一致。该病例强调了多模态成像在复杂神经管畸形管理中临床决策的重要性。