Multiple Sclerosis Revealed by Anterior Uveitis
نویسندگان
چکیده
منابع مشابه
Granuloma Annulare and Anterior Uveitis
Granuloma annulare is self-limiting cutaneous condition of unknown etiology, causing necrobiotic dermal and subcutaneous papules. A number of conditions have been described in association with Granuloma annulare, including lymphoma, anemia, intestinal bleeding, seronegative arthralgia, vasculitis and autoimmune thyroiditis. This manuscript, as the first report of this combination in Iran, descr...
متن کامل[Uveitis in patients with multiple sclerosis].
UNLABELLED Multiple sclerosis (SM) is an idiopathic, demyelinating CNS disease, with often ocular manifestations. Besides the most common SM ocular manifestation-optic neuritis, particular attention should be paid to uveitis. It is estimated that uveitis is ten times more frequent in population with SM than on population without it. PURPOSE The aim of this study is to present our own observat...
متن کاملUveitis in association with multiple sclerosis.
Rucker (I944) was first to describe sheathing of retinal veins in patients with multiple sclerosis. This was supported by later observers (Treusch and Rucker, 1944; Haar, I953; Scott, I96I), but the incidence was found to vary from IO to 23 per cent. It was initially thought that this periphlebitis was not associated with other ocular conditions, and might indicate a possible pathological basis...
متن کاملAcute Anterior Uveitis in a Patient Taking Fingolimod (FTY720) for Multiple Sclerosis
Fingolimod is an oral sphingosine-1-phosphate (S1P) receptor modulator and the first oral therapy for relapsing-remitting multiple sclerosis. Its use has been complicated by a low rate of cystoid macular edema usually in the first 3 months after commencement of the medication. We report the case of a 34-year-old male with relapsing-remitting multiple sclerosis, who developed acute anterior uvei...
متن کاملSystemic sclerosis sine scleroderma: a case report of anterior uveitis.
Systemic sclerosis (SSc) sine scleroderma (ssSSc) is characterized by the absence of skin involvement, despite other manifestations of systemic sclerosis are present. It is not known whether sSSc represents a forme fruste of limited cutaneous SSc or a distinct entity, but the 2013 American College of Rheumatology/European League Against Rheumatism criteria for the classification of SSc have con...
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ژورنال
عنوان ژورنال: European Journal of Medical and Health Sciences
سال: 2020
ISSN: 2593-8339
DOI: 10.24018/ejmed.2020.2.5.508