Gastrointestinal Involvement in Systemic Vasculitis
نویسنده
چکیده
Writing in the journal Current Opinion in Rheumatology Turkish researchers review the current literature on gastrointestinal involvement in different types of vasculitis. They address the variability of gastrointestinal involvement and of clinical findings, as well as treatment. An inflammatory bowel disease diagnosis usually precedes a diagnosis of vasculitis. A systematic review of the literature points to large vessel (mostly Takayasu arteritis), cutaneous vasculitis and ANCA-Associated Vasculitis (AAV) (mostly granulomatosis with polyangiitis, or GPA) as the three most common types of vasculitis associated with IBD. Primary vasculitides most commonly associated with a higher frequency of gastrointestinal involvement include immunoglobulin A (IgA) and anti-neutrophilic cytoplasmic antibodies (ANCA)-associated vasculitis (AAV), polyarteritis nodosa (PAN) and Behcet’s syndrome. Takayasu arteritis is associated with gastrointestinal symptoms that resemble inflammatory bowel diseases (IBD) in some patients. And, rheumatoid arthritis and systemic lupus erythematosus (SLE) can be associated with secondary vasculitis and gastrointestinal involvement. Patients with vasculitis symptoms typically experience abdominal pain, fever, diarrhea, nausea, vomiting and sometimes bleeding. They can also experience aneurysms or occlusions in mesenteric, hepatic or splenic vessels. An accurate diagnosis is difficult and usually includes imaging which may reveal an inflamed gastrointestinal tract with erosions, or ulcers that can lead to perforation, bleeding and bowel obstruction. Currently angiography is the gold standard for diagnosis of mesenteric vascular lesions especially if endovascular therapeutic interventions are needed. Vasculitis of solid organs in the pancreas, liver and gallbladder can occur in patients as well. Treatment depends on the type of vasculitis and is usually with high-dose corticosteroids and immunosuppressives. This article sums up the review as follows:
منابع مشابه
Cryoglobulinic Vasculitis in Children (Case Report)
Introduction: The systemic vasculitis have varicose etiology that most of them are caused by autoimmune problems. One kind of systemic vas is caused by the plenty amount of cryoglubulin in blood. Case report: A 3 year old boy with cutaneous, joint, and CNS manifestations that is diagnosed with cryoglubolinemic vasculitis. Discussion: Cryoglubolinemic vasculitis with CNS involvement and bleeding...
متن کاملHenoch-Schonlein Purpura—A Case Report and Review of the Literature
We describe a case of an adolescent male with Henoch-Schonlein purpura (HSP), presenting with cutaneous and gastrointestinal manifestations. Endoscopy revealed diffuse ulcerations in the stomach, duodenum, and right colon. Biopsies revealed a leukocytoclastic vasculitis in the skin and gastrointestinal tract. Steroid therapy led to complete resolution of the symptoms. HSP is the most common chi...
متن کاملLocalized vasculitis of the gastrointestinal tract: a case report and literature review.
Localized gastrointestinal vasculitis is a rare condition. It may be observed as an incidental unexpected pathologic finding at the time of biopsy of an abdominal mass or may present as unexplained abdominal pain with or without unexplained lower gastrointestinal bleeding. In this report we describe a new case of localized polyarteritis nodosa with involvement of peripancreatic middle-sized blo...
متن کاملThe manifestation of systemic vasculitis in the central nervous system--a case report.
We present a case of a patient with systemic vasculitis suffering--besides heart, skin and gastrointestinal lesions--from the rarely reported involvement of the central nervous system. Even though the diagnosis could not be ascertained precisely, immunosuppressive therapy led to prompt regression of symptoms including initially present neurologic manifestations.
متن کاملCutaneous Leukocytoclastic Vasculitis with Gastrointestinal Involvement after Anti-Tuberculosis Treatment
lamina propria (Figure 2B). The autoantibodies were not significantly increased. Anti-tuberculosis treatment was stopped, and the patient was started on methylprednisolone. This treatment relieved his skin lesions, abdominal pain. Follow-up esophagogastroduodenoscopy showed complete disappearance of all mucosal lesions. The patient fully met the criteria for CLV, as he was >16 years of age and ...
متن کامل