Intractable colitis associated with chronic granulomatous disease.

Abstract

The case of a 20-year-old Japanese man, diagnosed as having autosomal recessive chronic granulomatous disease (CGD), who was being treated with corticosteroids for intractable unclassified colitis, is described. He died from multiple organ failure following disseminated intravascular coagulation secondary to disseminated varicella-zoster virus (VZV) infection. He was diagnosed as an index case of CGD when 2 years old, was inoculated against VZV at the age of 5 years and had had an unremarkable course for 19 years. He was admitted to hospital because of a third episode of recurrent bloody diarrhoea. Clinical remission for each episode was achieved by intravenous corticosteroid therapy. Unclassified colitis associated with CGD was diagnosed based on a colonic biopsy demonstrating characteristic macrophages with lipofuscin deposits. From a treatment viewpoint, idiopathic inflammatory bowel disease (IBD) should be differentiated from secondary IBD occurring in CGD, in which immunosuppressive drugs including corticosteroids, still the mainstay of IBD treatment, should be avoided.

Cite this paper

@article{Arimura2006IntractableCA, title={Intractable colitis associated with chronic granulomatous disease.}, author={Yoshiaki Arimura and Akira Goto and Kentaro Yamashita and Takao Endo and Hideyuki Ikeda and Kaori Tanaka and Hiroyuki Tsutsumi and Yasuhisa Shinomura and Kohzoh Imai}, journal={Journal of medical microbiology}, year={2006}, volume={55 Pt 11}, pages={1587-90} }