Transanal endorectal pullthrough for hirschsprung disease: optimizing outcomes, reducing complications, and strengthening surgical care in resource-limited settings

<p><strong>Background:</strong> Hirschsprung’s disease (HD) is a congenital absence of enteric ganglion cells, leading to distal bowel obstruction, chronic constipation, and progressive proximal colonic dilation. In resource-limited settings, delayed presentation and limited pathology support often necessitate staged procedures, increasing morbidity and caregiver burden. Single-stage transanal endorectal pull-through (TAPT) offers a minimally invasive alternative that avoids laparotomy and colostomy.</p> <p><strong>Methods:</strong> This mixed prospective-retrospective case series included eight children (ages 2.5–9 years) with rectosigmoid HD who underwent single-stage TAPT between September 2024 and July 2025. Preoperative optimization involved rectal irrigations, nutritional rehabilitation, intravenous antibiotics, and fluid-electrolyte correction. Diagnosis was confirmed by contrast enema and full-thickness rectal biopsy. TAPT was performed using a Soave-type technique without intraoperative frozen section. Outcomes assessed included stool frequency, continence, enterocolitis episodes, anastomotic complications, weight gain, and quality of life.</p> <p><strong>Results:</strong> All patients presented with chronic constipation and abdominal distension. Median length of resected bowel was 20 cm. Time to first stool ranged 24–48 hours. One patient (12.5%) developed mild Hirschsprung-associated enterocolitis, successfully managed conservatively. No anastomotic leaks, strictures, or fecal incontinence occurred. At 3–6 months, all patients passed 1–2 soft stools daily, demonstrated improved weight gain, and achieved normal continence.</p> <p><strong>Conclusion:</strong> Single-stage TAPT is a safe and effective surgical option for rectosigmoid HD in resource-limited settings. Even without frozen section support and with delayed presentation, TAPT provides excellent early functional outcomes, minimal morbidity, and reduced hospitalization. This approach should be strongly considered as first-line management for rectosigmoid HD in similar environments.</p>

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Journal
European Journal of Medical Case Reports
Published
2026-04-13
DOI
https://doi.org/10.24911/ejmcr.9-2443
Primary Topic
Congenital gastrointestinal and neural anomalies
Type
article
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article

Transanal endorectal pullthrough for hirschsprung disease: optimizing outcomes, reducing complications, and strengthening surgical care in resource-limited settings

Alex Mashaka, Ally Mwanga, Mathayo Shadrack, Zaitun Bokhary et al.
European Journal of Medical Case Reports
Congenital gastrointestinal and neural anomalies
article

Transanal endorectal pullthrough for hirschsprung disease: optimizing outcomes, reducing complications, and strengthening surgical care in resource-limited settings

Alex Mashaka, Ally Mwanga, Mathayo Shadrack, Zaitun Bokhary, M Salim
article en

Abstract

<p><strong>Background:</strong> Hirschsprung’s disease (HD) is a congenital absence of enteric ganglion cells, leading to distal bowel obstruction, chronic constipation, and progressive proximal colonic dilation. In resource-limited settings, delayed presentation and limited pathology support often necessitate staged procedures, increasing morbidity and caregiver burden. Single-stage transanal endorectal pull-through (TAPT) offers a minimally invasive alternative that avoids laparotomy and colostomy.</p> <p><strong>Methods:</strong> This mixed prospective-retrospective case series included eight children (ages 2.5–9 years) with rectosigmoid HD who underwent single-stage TAPT between September 2024 and July 2025. Preoperative optimization involved rectal irrigations, nutritional rehabilitation, intravenous antibiotics, and fluid-electrolyte correction. Diagnosis was confirmed by contrast enema and full-thickness rectal biopsy. TAPT was performed using a Soave-type technique without intraoperative frozen section. Outcomes assessed included stool frequency, continence, enterocolitis episodes, anastomotic complications, weight gain, and quality of life.</p> <p><strong>Results:</strong> All patients presented with chronic constipation and abdominal distension. Median length of resected bowel was 20 cm. Time to first stool ranged 24–48 hours. One patient (12.5%) developed mild Hirschsprung-associated enterocolitis, successfully managed conservatively. No anastomotic leaks, strictures, or fecal incontinence occurred. At 3–6 months, all patients passed 1–2 soft stools daily, demonstrated improved weight gain, and achieved normal continence.</p> <p><strong>Conclusion:</strong> Single-stage TAPT is a safe and effective surgical option for rectosigmoid HD in resource-limited settings. Even without frozen section support and with delayed presentation, TAPT provides excellent early functional outcomes, minimal morbidity, and reduced hospitalization. This approach should be strongly considered as first-line management for rectosigmoid HD in similar environments.</p>

European Journal of Medical Case ReportsVol. 10(5)
Muhimbili University of Health and Allied Sciences (TZ)
Zero hunger
Openalex Percentile: Top 24%
Congenital gastrointestinal and neural anomalies
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