Objective: To investigate the diagnosis and surgical treatment of adult Hirschsprung disease (AHD).
Methods: Clinical data of 10 patients with AHD undergoing operation from May 1985 to May 2005 were analyzed retrospectively.
Results: There were 7 males and 3 females with an age ranged from 14 to 40 years. All the cases had constipation, and were diagnosed by barium enema. Aganglionosis was located in distal sigmoid and rectum in 2 cases, in rectum in 7 cases, unknown in one case. Colostomy was performed in one, Ikeda s operation in 6, Rehbein operation in two,modified Swenson operation in one. After radical operation,7 patients had excellent continence function, one had good function, one had poor function.
Conclusions: The diagnosis of adult HD mainly depends on the history of constipation, barium enema and manometry examination. The pull-through procedures are effective surgical treatments for adult HD. The operation type should be selected individually.
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Pediatr Surg Int
December 2024
Department of Gastrointestinal and Pediatric Surgery, Oslo University Hospital, Rikshopitalet, Postboks 4950 Nydalen, 0424, Oslo, Norway.
Med Int (Lond)
November 2024
Division of Pathology, Hospital Angeles Chihuahua, 31217 Chihuahua, Chih., Mexico.
J Pediatr Surg
October 2024
Pediatric Surgery, Medical Center of the Johannes-Gutenberg-University Mainz, Mainz, Germany; Pediatric Surgery, Hannover Medical School, Hannover, Germany.
Aim: Enterostomy takedown is common in neonates with Hirschsprung's disease, anorectal malformations, or necrotizing enterocolitis. Stapled bowel anastomosis has become routine in adults, but size of up to 12 mm diameter precludes performing enterostomy takedown in young infants using regular intestinal staplers. After the introduction of miniature (5 mm diameter) staplers, we increasingly used them for enterostomy takedown.
View Article and Find Full Text PDFMultiple endocrine neoplasia type 2 (MEN2) is the collective term for two distinct types of autosomal dominantly inherited neuroendocrine neoplasm syndromes: MEN2A and MEN2B (or MEN3). MEN2 is characterised by medullary thyroid cancer (MTC) (99%) and phaeochromocytoma (50%) and also other conditions according to specific genotype. MEN2A also includes a 25% risk of developing parathyroid hyperplasia and is now recognised as four separate syndromes: classic MEN2A, MEN2A with cutaneous lichen amyloidosis, MEN2A with Hirschsprung's disease and familial MTC.
View Article and Find Full Text PDFChildren (Basel)
October 2024
Great Ormond Street Hospital for Children, London WC1N 3JH, UK.
A growing number of patients with Hirschsprung disease are reaching adulthood, of whom a significant minority will require ongoing input from healthcare providers. In order to ensure patients receive the best care possible, it is essential to transition patients appropriately to adult services. This article describes the unmet need and some of the obstacles to this process and explores potential solutions, drawing on model examples for transitional care.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!