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Type IV Ehlers-Danlos syndrome: a surgical emergency

Q2: Comment on the history and computed tomogram
There was no evidence of perforative peritonitis. The computed tomogram (see p502) shows a large retroperitoneal haematoma around the aorta, but no aortic aneurysm. Spontaneous retroperitoneal bleeding is often associated with type IV Ehlers-Danlos syndrome and is the commonest cause of death in this population.

Discussion
Ehlers-Danlos syndrome is an inherited disorder of collagen synthesis. Type IV, far less common than types I, II and III, is caused by a deficiency of type III collagen.² The causative mutations in the COL3A1 gene are very variable, and are usually inherited in an autosomal dominant pattern. Biochemical examination in the present case showed the secretion of an abnormal type III collagen protein.³ DNA sequencing of cDNA produced from cultured skin fibroblasts showed a glycine (GGA) to glutamic acid (GAA) substitution at position 847 of the COL3A1 gene (fig 1). In keeping with other helical glycine substitutions, this causes severe reduction of tissue type III collagen, resulting in severely weakened arteries, intestines, ligaments, and other organs. We also detected similar changes in his mother and brother, while his maternal grandmother was a clinically silent somatic/gonadal mosaic for the error.³

View larger version (55K): [in this window] [in a new window]   Figure 1 Sequencing of DNA from patient’s cultured skin fibroblasts (reproduced from Human Genetics 1992;89:414–18, with permission from Springer Verlag, Berlin).

The present case demonstrates most of the complications that are associated with this unfortunate condition. It is due to a high incidence of these catastrophic complications that the life expectancy of patients with type IV Ehlers-Danlos syndrome is markedly shortened. They usually die in the fourth decade of life and survival beyond the age of 50 is rare. This contrasts with other Ehlers-Danlos syndrome variants who have normal life expectancy.

Awareness and early recognition of these life threatening complications are essential to the management of this unfortunate group of patients. Elective surgery should be undertaken with great caution, and only if absolutely necessary, as they tend to bleed uncontrollably and heal poorly after operations.

Final diagnosis
Spontaneous retroperitoneal bleeding associated with type IV Ehlers-Danlos syndrome.

References

1. Risaliti A, De Anna D, Terrosu G, et al. Chilaiditi’s syndrome as a surgical and nonsurgical problem. Surg Gynecol Obstet 1993;176:55–8.[Medline]
2. Pope FM, Martin GR, Lichtenstein JR, et al. Patients with Ehlers-Danlos syndrome type IV lack type III collagen. Proc Natl Acad Sci USA 1975;72:1314–6.[Abstract/Free Full Text]
3. Richards AJ, Ward PN, Narcisi P, et al. A single base mutation in the gene for type III collagen (COL3A1) converts glycine 847 to glutamic acid. Hum Genet 1992;89: 414–8.[Medline]
4. Hunter GC, Malone JM, Moore WS, et al. Vascular manifestations in patients with Ehlers-Danlos syndrome. Arch Surg 1982;117:495–8.[Medline]
5. Berney T, La Scala G, Vettorel D, et al. Surgical pitfalls in a patient with type IV Ehlers-Danlos syndrome and spontaneous colonic rupture. Dis Colon Rectum 1994;37:1038–42.[Medline]
6. Weinbaum PJ, Cassidy SB, Campbell WA, et al. Pregnancy management and successful outcome of Ehlers-Danlos syndrome type IV. Am J Perinatol 1987;4:134–7.[Medline]

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