| Literature DB >> 35340639 |
Faten Limaiem1,2, Kaouther Dimassi1,3.
Abstract
Craniorachischisis totalis is an uncommon and severe form of neural tube defect. It is characterized by anencephaly and spina bifida throughout the vertebral column accompanied by herniation of neural tissue and meninges. Hepatic calcification in the fetus is rare and its clinical significance is not fully established.Entities:
Keywords: anencephaly; antenatal diagnosis; craniorachischisis; liver calcifications; neural tube defects
Year: 2022 PMID: 35340639 PMCID: PMC8929274 DOI: 10.1002/ccr3.5606
Source DB: PubMed Journal: Clin Case Rep ISSN: 2050-0904
FIGURE 1(A) Ultrasonographic view of the fesstus with total craniorachischisis. (B) Frontal view of the fetus showing anencephaly. The orbit is partially formed, with bulging eyes. The cranial vault is absent (acrania) and the skull base flattened. (C) Posterior view of the fetus showing complete division of the spine: total spina bifida in the fetus of 14 weeks +3 days of gestational age. There is complete failure of neural tube closure, exposing the spinal cord. There has been no fusion of the rostral tube, resulting in abnormal development and damage of the forebrain structures which are replaced by hemorrhagic tissue. (D), Foci of hepatic calcifications were noted in the liver parenchyma (black arrow) (Hematoxylin and eosin, magnification ×200)