Hirschsprung disease and anorectal malformations — An uncommon association
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Read the article on jpedsurg.org ↗Article · Jun 2020 · 1 min read
In brief
In brief
Large cohort study demonstrates that concurrent Hirschsprung disease and anorectal malformation occurs in only 0.17% of ARM patients, far less common than previously reported. Highlights diagnostic pitfall: rectal biopsies in ARM patients may falsely appear aganglionotic, risking unnecessary pull-through procedures that cause incontinence.
Written by the GCMD Library team from the article.
Abstract
Background
The simultaneous occurrence of Hirschsprung disease (HD) and anorectal malformation (ARM) is extremely rare, with only a very limited amount of cases published in the literature.
Constipation is a major problem in patients operated for ARM, and biopsies from the distal rectum in patients with ARM may not show ganglion cells owing to different reasons, leading to a false positive diagnosis of HD. A pull-through procedure for HD after previous anorectoplasty for ARM always leads to fecal incontinence.
The aim of the present study was to assess the incidence of simultaneous diagnoses of ARM and HD in a single large cohort of ARM patients and to demonstrate that biopsies from the anal canal, which are negative for ganglion cells, may mislead to a diagnosis of HD.
Materials and methods
A retrospective review of our database from 1980 to 2018 identified 164 patients with HD and 2397 patients with ARM. Four patients suffered from both HD and ARM.
Results
The incidence of HD in ARM patients was 4/2397 = 0.17%, and the incidence of ARM in HD patients was 4/164 = 2.4%.
Conclusion
Our results strongly suggest that the association of ARM and HD is less common than previously reported.
Type of study
Therapeutic
Level of evidence
IV