The Ehlers-Danlos syndrome and colonic perforation
- 1 December 1985
- journal article
- research article
- Published by Wolters Kluwer Health in Diseases of the Colon & Rectum
- Vol. 28 (12) , 962-966
- https://doi.org/10.1007/bf02554318
Abstract
The Ehlers-Danlos syndrome is a genetically determined disorder of connective tissue which is generally known for its features of fragile, hyperextensible skin, hypermobile joints, and tissue fragility. Less commonly, colorectal complications can occur, including bleeding, prolapse, and diverticulitis. A rare case of colonic perforation associated with Ehlers-Danlos syndrome is presented. Additionally, in vitro electromyographic studies of the colonic tissue were performed which suggested a possible link between abnormal myogenic activity and the colonic perforations. The authors recommended that treatment be either a permanent colostomy of a subtotal colectomy with anastomosis to the rectum for similar cases.This publication has 4 references indexed in Scilit:
- Electrophysiologic control of motility in the human colonGastroenterology, 1985
- Colon perforation in Ehlers-Danlos syndrome: Report of two cases and review of the literatureThe American Journal of Surgery, 1984
- Gastrointestinal complications of the Ehlers-Danlos syndromeGut, 1969