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Ependymoblastomatous exencephaly: a unique fetal malformation.
- 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."
- Subjects :
- Anencephaly ultrastructure
Congenital Abnormalities ultrastructure
Fatal Outcome
Female
Humans
Neural Tube Defects ultrastructure
Neuroectodermal Tumors, Primitive ultrastructure
Pregnancy
Pregnancy Trimester, First
Anencephaly pathology
Congenital Abnormalities pathology
Fetus pathology
Neural Tube Defects pathology
Neuroectodermal Tumors, Primitive pathology
Subjects
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