Back to Search Start Over

Ependymoblastomatous exencephaly: a unique fetal malformation.

Authors :
Mittelbronn M
Wolburg H
Kendziorra H
Stopper E
Sousa P
Rorke-Adams LB
Source :
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society [Pediatr Dev Pathol] 2008 Sep-Oct; Vol. 11 (5), pp. 397-401. Date of Electronic Publication: 2008 Feb 11.
Publication Year :
2008

Abstract

Exencephaly/anencephaly is a rare neural tube defect occurring early in embryogenesis. We report a 14-week-old fetus with exencephaly in whom central nervous system tissue was developed and preserved. There were 2 symmetrical structures grossly resembling cerebral hemispheres, which on histologic and ultrastructural study, consisted of a combination of ependymoblastomatous rosettes and canals and primitive neural tissue. The brainstem and spinal cord were partially normally formed, although descending tracts were not apparent. No cerebellar tissue was found. The eyes were formed. This appears to represent a rare example of exencephaly not covered by skin, which did not undergo necrosis and early transformation into a residual area cerebrovasculosa, characteristic of anencephaly. It may be appropriate to regard this as a unique neural tube closure defect that might be termed "ependymoblastomatous exencephaly."

Details

Language :
English
ISSN :
1093-5266
Volume :
11
Issue :
5
Database :
MEDLINE
Journal :
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
Publication Type :
Academic Journal
Accession number :
18078364
Full Text :
https://doi.org/10.2350/07-06-0295.1