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DOI 10.1177/10935266211053973

Медицинская библиотека · Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society · 2021

Characterization of the Transition Zone in Short Segment Hirschsprung Disease Using Calretinin Immunostaining.

Righini-Grunder Franziska, Bouron-Dal Soglio Dorothée, Hart Lara, Aspirot Ann, Faure Christophe, Patey Natacha

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Аннотация

Introduction

The detailed expression pattern of calretinin immunohistochemistry in the transition zone (TZ) of Hirschsprung disease (HSCR) has not yet been reported. This study aims to examine the value of calretinin immunohistochemistry for more accurately determining the distal and proximal border of the TZ in short segment HSCR.

Methods

Specimens of pull-through surgery from 51 patients with short form of HSCR were analyzed on two longitudinal strips using hematoxylin and eosin (H&E) staining and calretinin immunohistochemistry.

Results

In all but two patients, the first appearance of calretinin expression was seen on mucosal nerve fibers before the appearance of any ganglion cells, indicating the distal border of the TZ. The maximum distance between the distal border of the TZ and the proximal border of the TZ, defined by ganglion cells in a normal density on H&E stained sections, a strong calretinin expression on mucosal nerve fibers and in >80% of submucosal and myenteric ganglion cells, with no nerve hypertrophy and absence of ganglionitis was 60 mm.

Conclusion

The distal border of the TZ is characterized by calretinin positive intramucosal neurites in nearly all of short form of HSCR and not by calretinin expression on ganglion cells.

Для цитирования: Righini-Grunder Franziska, Bouron-Dal Soglio Dorothée, Hart Lara, Aspirot Ann, Faure Christophe, Patey Natacha. Characterization of the Transition Zone in Short Segment Hirschsprung Disease Using Calretinin Immunostaining.. Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society. 2021. DOI: 10.1177/10935266211053973.

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