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[Spontaneous colonic perforations revealing Ehlers-Danlos syndrome type IV] Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie. [Arch Pediatr] Journal article

 
Henry C, Geiss S, Wodey E, Pennerath A, Zabot MT, Peyrol S, Plauchu H 
[Spontaneous colonic perforations revealing Ehlers-Danlos syndrome type IV] [Case Reports, Journal Article, Review]
Arch Pediatr 1995 Nov; 2(11):1067-72.


BACKGROUND--The malignant form of Ehlers-Danlos syndrome type IV owes its bad reputation to a proneness to spontaneous rupture of bowel or large vessels, which may reveal the disease. CASE REPORT--A girl suffered acute rupture of the sigmoid at the age of 5 years and rupture of the left colon, twice, at the age of 11 and 13 years, respectively. These ruptures required colostomy and finally colectomy. A proneness to bruisability, history of dislocation of hips, hypermobile joints, ovarian cysts and some minor abnormalities of her face resembled that of the Ehlers-Danlos syndrome which was confirmed by optic and electronic microscopy of the skin biopsy. CONCLUSION--This is the youngest case of rupture of bowel reported in Ehlers-Danlos syndrome. Long-term prognosis is influenced by repetition of intestinal ruptures and occurrence of vascular complications.



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