Hirschprung disease here classification: Difference between revisions
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Created page with "__NOTOC__ {{Hirschprung disease}} {{CMG}}; {{AE}} {{AY}} ==Overview== ==References== {{WH}} {{WS}}" |
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==Overview== | ==Overview== | ||
==Classification== | |||
Based on the extent of colon involvement Hirschsprung's disease can be classified into the following: | |||
*'''Rectosigmoid form:''' It is the most common form and is seen in 80 to 75% of infants diagnosed with Hirschsprung's disease. | |||
*'''Long segment colonic Hirschsprung disease''' | |||
*'''Total colonic aganglionosis with ileal involvement upto 50 cm proximal to the ileocecal junction:''' It is uncommon and accounts for 5 to 7% of cases diagnosed with Hirschsprung's disease. | |||
==References== | ==References== | ||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
Revision as of 18:33, 13 June 2017
Template:Hirschprung disease Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Younes M.B.B.CH [2]
Overview
Classification
Based on the extent of colon involvement Hirschsprung's disease can be classified into the following:
- Rectosigmoid form: It is the most common form and is seen in 80 to 75% of infants diagnosed with Hirschsprung's disease.
- Long segment colonic Hirschsprung disease
- Total colonic aganglionosis with ileal involvement upto 50 cm proximal to the ileocecal junction: It is uncommon and accounts for 5 to 7% of cases diagnosed with Hirschsprung's disease.