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Stillborn or liveborn? Comparing umbilical cord immunohistochemical expression of vitality markers (tryptase, alpha(1)-antichymotrypsin and CD68) by quantitative analysis and confocal laser scanning microscopy

NERI, MARGHERITA
•
D'ERRICO, STEFANO
•
FIORE, CARMELA
altro
FINESCHI, VITTORIO
2009
  • journal article

Periodico
PATHOLOGY RESEARCH AND PRACTICE
Abstract
The distinction between stillborn and liveborn infants and the demonstration of a separate existence of fetuses are central issues in the daily practice of perinatologists and pathologists. The current knowledge about the chronology of responses of the tissue following the occurrence of a vital reaction, as well as the existence of numerous studies that aimed at identifying markers of vitality of cutaneous lesions, induced us to investigate the umbilical cord for the presence or absence of vitality indexes. We investigated 45 samples of umbilical cords obtained during post-mortem examinations of stillborns, as well as samples of umbilical cords taken from newborns after normal labor. On these samples, we performed a complete immunohistochemical study. Our results showed that some of the parameters investigated, such as tryptase for the mast cell, CD68, and alpha-1-antichymotrypsin, showed a statistically significant (po0.0001) different expression in the two groups under study (stillborn and liveborn). Owing to the strong different expression of these markers in the samples of the umbilical cords from liveborns, compared to those from stillborns, one might regard them as reliable parameters, to which the pathologist may resort whenever he is dealing with the distinction between stillborns and liveborns.
DOI
10.1016/j.prp.2009.01.011
WOS
WOS:000268620900003
Archivio
http://hdl.handle.net/11368/2959972
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-67649554231
Diritti
metadata only access
Soggetti
  • Stillborn

  • Liveborn

  • Umbilical cord

  • Immunohistochemistry

  • Confocal laser scanni...

Web of Science© citazioni
4
Data di acquisizione
Mar 27, 2024
Visualizzazioni
1
Data di acquisizione
Apr 19, 2024
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