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Immunohistochemical and Histopathological Characterization of Spina Bifida Defect Tissues Removed After Prenatal and Postnatal Surgical Repair.
Bardill, James R; Laughter, Melissa R; Anderson, Jaclyn B; Hoffman, Hilary; Gilani, Ahmed; Koster, Maranke I; Marwan, Ahmed I.
Afiliación
  • Bardill JR; Department of Surgery, Division of Pediatric Surgery, University of CO Denver Anschutz Medical Campus, Aurora, CO, USA.
  • Laughter MR; University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO, USA.
  • Anderson JB; Department of Pathology, School of Medicine, Stanford University, Stanford, CA, USA.
  • Hoffman H; Department of Surgery, Division of Pediatric Surgery, University of CO Denver Anschutz Medical Campus, Aurora, CO, USA.
  • Gilani A; Department of Pathology, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, USA.
  • Koster MI; Department of Biochemistry and Molecular Biology, Brody School of Medicine, East Carolina University, Greenville, NC, USA.
  • Marwan AI; Department of Surgery, Division of Pediatric Surgery, University of MO School of Medicine, Columbia, MO, USA.
Fetal Pediatr Pathol ; 43(3): 225-233, 2024.
Article en En | MEDLINE | ID: mdl-38634787
ABSTRACT

Background:

Myelomeningocele or spina bifida is an open neural tube defect that is characterized by protrusion of the meninges and the spinal cord through a deformity in the vertebral arch and spinous process. Myelomeningocele of post-natal tissue is well described; however, pre-natal tissue of this defect has no known previous histologic characterization. We compared the histology of different forms of pre-natal myelomeningocele and post-natal myelomeningocele tissue obtained via prenatal intrauterine and postnatal surgical repairs.

Methods:

Pre-and post-natal tissues from spina bifida repair surgeries were obtained from lipomyelomeningocele, myeloschisis, and myelomeningocele spina bifida defects. Tissue samples were processed for H&E and immunohistochemical staining (KRT14 and p63) to assess epidermal and dermal development.

Results:

Prenatal skin near the defect site develops with normal epidermal, dermal, and adnexal structures. Within the grossly cystic specimens, histology shows highly dense fibrous connective tissue with complete absence of a normal epidermal development with a lack of p63 and KRT14 expression.

Conclusion:

Tissues harvested from prenatal and postnatal spina bifida repair surgeries appear as normal skin near the defect site. However, cystic tissues consist of highly dense fibrous connective tissue with complete absence of normal epidermal development.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inmunohistoquímica / Disrafia Espinal / Meningomielocele Límite: Female / Humans / Newborn / Pregnancy Idioma: En Revista: Fetal Pediatr Pathol Asunto de la revista: PATOLOGIA / PEDIATRIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inmunohistoquímica / Disrafia Espinal / Meningomielocele Límite: Female / Humans / Newborn / Pregnancy Idioma: En Revista: Fetal Pediatr Pathol Asunto de la revista: PATOLOGIA / PEDIATRIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos
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