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Title: [Spontaneous colonic perforations revealing Ehlers-Danlos syndrome type IV]. Author: Henry C, Geiss S, Wodey E, Pennerath A, Zabot MT, Peyrol S, Plauchu H. Journal: Arch Pediatr; 1995 Nov; 2(11):1067-72. PubMed ID: 8547975. Abstract: 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.[Abstract] [Full Text] [Related] [New Search]