Systemic vasculitis is generally believed to be an immune complex deposition in blood vessels. Gastrointestinal complications of vasculitis have been described as pain, diarrhea, rectal bleeding and abnormal liver enzymes. Taken in isolation, the symptoms are difficult to distinguish from inflammatory bowel disease, infectious colitis or ischemic colitis, although gastrointestinal vasculitis rarely presents without other clinical evidence of systemic vasculitis. Histo- logical proof is difficult to obtain because biopsies from the gastrointestinal tract usually show only nonspecific inflammation and ulceration. Camilleri and Pusey suggested that this may be because endoscopic biopsies are too superficial and proposed that endoscopic examination was the best method to determine extent of disease. Diagnosis is often made clinically from the involvement of other organ systems because biopsies frequently show no evidence of a specific vasculitis. Therapy is aimed at treating the systemic vasculi- tis with immunosuppressive medications and with surgical intervention in the event of gastrointestinal complications such as hemorrhage or perforation.
Vasculitic involvement of the gastrointestinal tract is more common in polyarteritis nodosa and microscopic polyarteritis (50% to 70%) and Chrug-Strauss syndrome (20%) than in Wegener’s granulomatosis. Walton published autopsy studies of patients with Wegener’s granu- lomatosis and found gastrointestinal involvement in 24%, although none of these patients had symptoms referable to the gastrointestinal tract. Two large groups of patients with We- gener’s granulomatosis have been followed for over 20 years, and neither study describes gastrointestinal complications throughout the course of the disease. Case reports of gastrointestinal involvement in Wegener’s granulomatosis have described cases of enterocolitis, gastrointestinal hemorrhage, intestinal perforation and recurrent pancreatitis.
































