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INTRODUCTION: Renal involvment of Behçet disease is not usual and Ig A vasculitis complicated by Behçet disease is extremely rare. CASE PRESENTATION: We report a case of Henoch Scholein purpura and nephritis associated with Behçet disease revealed by ophthalmic examination. CLINICAL DISCUSSION: Recurrent oral ulcer is not a manifestation of Ig A vasculitis which doesn't affect large or middle sized arteries. If the patient had'nt been referred to our department for ophthalmic examination, we may have failed to make the diagnosis and treat coexisting Behçet disease. CONCLUSION: The link of HSP and BD has yet to be fully understood, and more researchisdefinitelyneeded.
RESUMO
INTRODUCTION: Retinal vasoproliférative tumors (VPTs) have been reported as uncommon complications of intermediate Uveitis. CASE DESCRIPTION: A patient consulted for a gradually decreased vision in the right eye (RE). The examination of the RE found a corrected visual acuity at 20/100 with normal eye pressure measured. The anterior segment was deep and quiet and 2+ vitreous haze was found. Funduscopy showed a VPT. Retinal fluorescein angiography of the RE revealed macular cystoid edema also objectified by the Optical Coherence Tomography (OCT). Intermediate Uveitis was considered idiopathic. The patient received a cryoapplication and was put on oral corticosteroid therapy with improvement of visual acuity and a regress of both vitreous inflammation and cystoid macular edema. CONCLUSION: The association of a VPT with intermediate uveitis represents a real diagnostic and therapeutic challenge and imposes rigorous care and monitoring strategy combining internist and ophthalmologist.
