Histopathological dimensions differ between aganglionic and ganglionic bowel wall in children with Hirschsprung's disease.

Aganglionosis Bowel wall Children Ganglionosis Hirchsprung’s disease Histopathology

Journal

BMC pediatrics
ISSN: 1471-2431
Titre abrégé: BMC Pediatr
Pays: England
ID NLM: 100967804

Informations de publication

Date de publication:
20 12 2022
Historique:
received: 10 09 2022
accepted: 06 12 2022
entrez: 19 12 2022
pubmed: 20 12 2022
medline: 22 12 2022
Statut: epublish

Résumé

In the validation of new imaging technology for children with Hirschsprung's disease (HSCR), basic anatomical parameters of the bowel wall must be established specifically for this patient group. To explore differences in histoanatomical layers of bowel wall, comparing ganglionic and aganglionic bowel walls, and to examine if the bowel wall thickness is linked to patient weight. This was an observational study of bowel specimens from children weighing 0-10 kg, operated on consecutively during 2018-2020. Ganglionic and aganglionic bowel walls were measured in digitalized microscopy images from 10 sites per trans-sectional specimen and compared regarding the thickness of their histoanatomical layers. Bowel walls were measured in 21 children. Full bowel wall thickness did not differ between aganglionic and ganglionic bowel (2.20 vs 2.04; p = 0.802) while weight at surgery correlated positively with both ganglionic and aganglionic bowel wall thickness (r = 0.688 and 0.849, respectively), and age at surgery with ganglionic bowel wall thickness (r = 0.517). In aganglionic segments, the muscularis externa layer was thicker compared to that in ganglionosis (0.45 vs 0.31 mm, p = 0.012) whereas the muscularis interna was thinner (0.45 vs 0.62 mm, p < 0.001). A diagnostic index was identified whereby a lower ratio of muscularis interna/externa thickness followed by a thinner muscularis interna differed between aganglionic and ganglionic bowel in all specimens. Thicknesses of the bowel wall's muscle layers differ between aganglionic and ganglionic bowel walls in children with HSCR. These findings support a diagnostic index that could be validated for transfer to instant diagnostic imaging techniques. Diagnostic: 3.

Sections du résumé

BACKGROUND
In the validation of new imaging technology for children with Hirschsprung's disease (HSCR), basic anatomical parameters of the bowel wall must be established specifically for this patient group.
AIM
To explore differences in histoanatomical layers of bowel wall, comparing ganglionic and aganglionic bowel walls, and to examine if the bowel wall thickness is linked to patient weight.
METHODS
This was an observational study of bowel specimens from children weighing 0-10 kg, operated on consecutively during 2018-2020. Ganglionic and aganglionic bowel walls were measured in digitalized microscopy images from 10 sites per trans-sectional specimen and compared regarding the thickness of their histoanatomical layers.
RESULTS
Bowel walls were measured in 21 children. Full bowel wall thickness did not differ between aganglionic and ganglionic bowel (2.20 vs 2.04; p = 0.802) while weight at surgery correlated positively with both ganglionic and aganglionic bowel wall thickness (r = 0.688 and 0.849, respectively), and age at surgery with ganglionic bowel wall thickness (r = 0.517). In aganglionic segments, the muscularis externa layer was thicker compared to that in ganglionosis (0.45 vs 0.31 mm, p = 0.012) whereas the muscularis interna was thinner (0.45 vs 0.62 mm, p < 0.001). A diagnostic index was identified whereby a lower ratio of muscularis interna/externa thickness followed by a thinner muscularis interna differed between aganglionic and ganglionic bowel in all specimens.
CONCLUSION
Thicknesses of the bowel wall's muscle layers differ between aganglionic and ganglionic bowel walls in children with HSCR. These findings support a diagnostic index that could be validated for transfer to instant diagnostic imaging techniques.
LEVEL OF EVIDENCE
Diagnostic: 3.

Identifiants

pubmed: 36536313
doi: 10.1186/s12887-022-03792-3
pii: 10.1186/s12887-022-03792-3
pmc: PMC9764572
doi:

Types de publication

Observational Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

723

Informations de copyright

© 2022. The Author(s).

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Auteurs

Christina Graneli (C)

Department of Pediatric Surgery, Children's Hospital, Skåne University Hospital Lund, Lund University, Lund, Sweden.

Sofia Patarroyo (S)

Department of Pediatric Surgery, Children's Hospital, Skåne University Hospital Lund, Lund University, Lund, Sweden.

Rodrigo Munoz Mitev (RM)

Department of Clinical Genetics and Pathology, Skåne University Hospital, Lund University, Lund, Sweden.

David Gisselsson (D)

Department of Clinical Genetics and Pathology, Skåne University Hospital, Lund University, Lund, Sweden.

Emilia Gottberg (E)

Department of Clinical Genetics and Pathology, Skåne University Hospital, Lund University, Lund, Sweden.

Tobias Erlöv (T)

Department of Biomedical Engineering, Faculty of Engineering, LTH, Lund University, Lund, Sweden.

Tomas Jansson (T)

Department of Biomedical Engineering, Department of Clinical Engineering, Clinical Sciences Lund, LTH, Lund University, Skåne University Hospital, Lund, Sweden.

Kristine Hagelsteen (K)

Department of Pediatric Surgery, Children's Hospital, Skåne University Hospital Lund, Lund University, Lund, Sweden.

Magnus Cinthio (M)

Department of Biomedical Engineering, Faculty of Engineering, LTH, Lund University, Lund, Sweden.

Pernilla Stenström (P)

Department of Pediatric Surgery, Children's Hospital, Skåne University Hospital Lund, Lund University, Lund, Sweden. pernilla.stenstrom@med.lu.se.

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