Titlebook: Beh?et‘s Syndrome; From Pathogenesis to Lorenzo Emmi Book 2014 Springer-Verlag Italia 2014 Autoimmune disease.Autoinflammatory disease.Beh?

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,Intestinal Beh?et Disease,tis, epididymitis and mucocutaneous, articular, gastrointestinal, neurologic, and vascular manifestations [.]. Classified as a systemic vasculitis, it can involve both the arteries and veins of almost any organ. This is an analysis of intestinal involvement in BD.

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,Beh?et’s Disease. Differential Diagnosis,l ulceration, and eye disease represent the classic triad of manifestations, the cardiovascular, gastrointestinal, musculoskeletal, and central nervous systems can also be affected. Thus the differential diagnosis of BD is complicated by the panopoly of clinical symptoms and signs and also by the un

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Prognosis and Disease Activity,nt the only clinical features in patients with a benign disease subset, there are other patients who develop potentially sight or life-threatening manifestations, due to ocular, neurological, or major vascular involvement. Beside the organ involvement, demographic factors could considerably influenc

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,Old and New Treatment for Beh?et’s Disease, manifestations. New topical therapies such as pimecrolimus and amlexanox are useful for oral and genital ulcers. Old systemic therapies, especially colchicine, azathioprine, and cyclosporine represent the first-line therapy in most cases. In presence of BD serious manifestations, including uveitis,

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