Fetal and Pediatric Pathology ( IF 0.7 ) Pub Date : 2022-06-07 , DOI: 10.1080/15513815.2022.2086330 Javier Arredondo Montero 1 , Mónica Bronte Anaut 2 , Carlos Bardají Pascual 1
Abstract
Background: Neuroglial heterotopia, characterized by mature neuroglial tissue outside the central nervous system, has not been previously associated with cranioschisis. Case Report: A 4-year-old female patient, with left congenital anophthalmia, had a nasofrontal neuroglial heterotopia protruding through an ossification defect. Discussion: Nasofrontal cranioschisis may be associated with neuroglial heterotopias. The combination of anophthalmia and neuroglial heterotopia, previously described only once in the literature, may be part of a broader malformation spectrum that has not been properly characterized to date.
中文翻译:
与硬膜外神经胶质细胞异位相关的单侧无眼症和先天性额骨裂:对可能的新畸形谱的新见解
摘要
背景:神经胶质异位症,其特征是中枢神经系统外的成熟神经胶质组织,以前未与颅分裂相关。病例报告:一名 4 岁女性患者,患有左侧先天性无眼症,鼻额神经胶质异位通过骨化缺损突出。讨论:鼻额颅裂可能与神经胶质异位有关。无眼畸形和神经胶质异位症的组合,以前在文献中仅描述过一次,可能是迄今为止尚未正确表征的更广泛的畸形谱的一部分。