Hirschsprung's disease: A 20-year experience
References (29)
- et al.
The extracellular matrix components, tenascin and fibronectin, in Hirschsprung's disease: An immunohistochemical study
J Pediatr Surg
(1994) - et al.
Ectopic class II major histocompatibility antigens in Hirschsprung's disease and neuronal intestinal dysplasia
J Pediatr Surg
(1992) - et al.
Nitric oxide synthase distribution in the enteric nervous system of Hirschsprung's disease
Gastroenterology
(1993) - et al.
A 7-year study of the diagnostic value of rectal mucosal acetylcholinesterase measurement in Hirshsprung's disease
J Pediatr Surg
(1987) - et al.
Total colectomy and ileorectal anastomosis in the treatment of total colonic aganglionosis: A long-term follow-up study of six patients
J Pediatr Surg
(1989) - et al.
High imperforate anus: Quantitative results of long-term fecal continence
J Pediatr Surg
(1985) Total colon aganglionosis preservation and utilization of entire colon
J Pediatr Surg
(1982)Hirschsprung's disease: One surgeon's experience in one institution
J Pediatr Surg
(1995)- et al.
Hirschsprung's disease: Associated abnormalities and demography
J Pediatr Surg
(1992) - et al.
Discordant Hirschsprung's disease in monozygotic twins: A clue to pathogenesis?
J Pediatr Surg
(1988)
Problems and pitfalls in the management of Hirschsprung's disease
J Pediatr Surg
Management of Hirschsprung's disease: Curative surgery before 3 months of age
J Pediatr Surg
Morbidity associated with total colon Hirschsprung's disease
J Pediatr Surg
Long-term results of surgical treatment in infants with total colonic aganglionosis
J Pediatr Surg
Cited by (95)
Nationwide outcomes of newborns with rectosigmoid versus long-segment Hirschsprung disease
2023, Journal of Pediatric SurgeryHirschsprung disease and Paediatric Intestinal Pseudo-obstruction
2022, Best Practice and Research: Clinical GastroenterologyCitation Excerpt :Although the delay in the passage of the first stool should not necessarily be interpreted as a sign of HSCR in healthy premature infants [2], the diagnosis should be considered where there is clinical concern. A recent systematic review in 4147 infants with HSCR, born between 1964 and 2013, found an overall prevalence of HSCR in preterm infants of 6% [11]. If the diagnosis is made later in childhood, the most common presenting symptom is long-standing refractory constipation, followed by abdominal distension, vomiting, failure to thrive and enterocolitis [3,15].
Management and outcomes for long-segment Hirschsprung disease: A systematic review from the APSA Outcomes and Evidence Based Practice Committee
2021, Journal of Pediatric SurgeryCitation Excerpt :Their report predominantly compared Soave to Duhamel for short segment disease, with their LSHD and TCHD numbers too small to determine a significant difference [24]. In a report of 9 children with LSHD where there were 3 Martin, 2 Swenson-Deloyers (complete right colon mobilization with preservation of the ileocolic artery and full-thickness coloanal anastomosis), 2 Swenson, and 2 ileostomy-alone, they found no technique to be satisfactory, with a preference towards the Martin procedure [25]. In a series of 48 TCHD patients, the average number of additional surgical procedures under anesthetic was 3.7 following a Soave operation (n = 3), 1.4 after a Martin procedure (n = 10), and 1.0 after standard Duhamel procedure (n = 14) [26].
Reducing Underdiagnosis of Hirschsprung-Associated Enterocolitis: A Novel Scoring System
2021, Journal of Surgical ResearchLong-term outcomes of laparoscope-assisted heart-shaped anastomosis for children with hirschsprung disease: A 10-year review study
2020, Journal of Pediatric SurgeryA rare case of rectal prolapse after Deloyers procedure in a patient with Hirschsprung's disease: A case report
2019, International Journal of Surgery Case ReportsCitation Excerpt :In some cases, obstruction progresses to intestinal perforation, leading to mortality. Commonly performed modes of operative treatment for Hirschsprung’s disease include the Swenson, Duhamel and Soave methods [3–5]. The goal of these procedures is to achieve anastomosis between functioning bowel to anus.