Publication: Immunohistochemical study of enteric nervous system in hirschsprung’s disease and intestinal neuronal dysplasia
Authors
Geramizadeh, Bita ; Akbarzadeh, Elahe ; Izadi, Babak ; Foroutan, Hamid-Reza ; Heidari, Tahere
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Publisher
F. Hernández y Juan F. Madrid. Universidad de Murcia. Departamento de Biología Celular e Histología
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DOI
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info:eu-repo/semantics/article
Description
Abstract
Background. Hirschsprung’s disease (HD) is
one of the most common motility disorders in pediatric
age groups and it is very important that it be
differentiated from other types of motility disorders,
especially intestinal neuronal dysplasia B (IND B).
Although many studies regarding the differences
between the two disorders by immunohistochemical
studies exist, there is as yet no consistent result. The
purpose of this research was to study the immunohistochemical
findings of enteric nervous system in these two
motility disorders in comparison with colectomies
without motility disorder. Methods. Full wall thickness
specimens of three groups of patients (HD, IND B and
non motility disorders) were included in the study to be
evaluated by immunohistochemistry (IHC). Markers
were specific for neuronal cells and pace maker cells
composed of PGP 9.5, c-kit, synaptophysin, S100 and
CD56. The number of cells was evaluated in the
muscularis properia, and myenteric plexus. Results. The
number of all the IHC markers i.e. PGP9.5, c-kit,
synaptophysin, S100 and CD56 was completely different
in HD from the two other groups, while IND B was quite
similar to control group. Conclusion. Our finding
suggests that there is a marked and significant difference
between HD and IND B by IHC markers, which can be
used as an additional test for the diagnosis of HD with
more accuracy. Further multicenter studies with a greater
number of cases would be necessary to find a cut-off
point for every IHC marker to differentiate HD and IND
B.
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Citation
Histology and histopathology, Vol. 28, n.º 3 (2013)
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