International Journal of Academic Medicine

: 2017  |  Volume : 3  |  Issue : 3  |  Page : 96--100

Hirschsprung's disease

Sangeetha Prabhakaran 
 Department of Surgery, University of North Dakota, Grand Forks; OPUS 12 Foundation, Grand Forks Chapter, ND, USA

Correspondence Address:
Sangeetha Prabhakaran
Department of Surgery, School of Medicine and Health Sciences, University of North Dakota, Room 5108, 501 North Columbia Road Stop 9037, Grand Forks ND 58203

Hirschsprung's disease (HD) or congenital aganglionic megacolon is characterized by an absence of ganglion cells in the myenteric Auerbach's plexus, the deep submucosal Henle's plexus, and the submucosal Meissner's plexus in the distal colon. The usual presentation of Hirschsprung's disease can be demonstrated by the following clinical scenario. A 3-day-old male presented with failure to pass meconium within 48 h of birth and progressive abdominal distension. Barium study showed dilated colon with no specific zone of transition. The newborn was delivered at 40 weeks gestation after an otherwise normal pregnancy. Transanal rectal biopsy demonstrated the absence of ganglion cells on multiple sections and special staining. The patient underwent an exploratory laparotomy, upon which he was found to have markedly dilated small bowel and colon up to the area of sigmoid. A transverse loop colostomy was performed. The patient recovered well from the initial surgery and underwent definitive surgical therapy of the HD at a later time. The following core competencies are addressed in this article: Medical knowledge, Patient care. Republished with permission from: Prabhakaran S. Absite corner: Hirschsprung's disease. OPUS 12 Scientist 2009; 3(3):44-46.

How to cite this article:
Prabhakaran S. Hirschsprung's disease.Int J Acad Med 2017;3:96-100

How to cite this URL:
Prabhakaran S. Hirschsprung's disease. Int J Acad Med [serial online] 2017 [cited 2023 Jan 27 ];3:96-100
Available from:;year=2017;volume=3;issue=3;spage=96;epage=100;aulast=Prabhakaran;type=0