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Published byJanis Perkins Modified over 9 years ago
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Behçet’s Disease: A Case of Peripheral Ulcerative Keratitis Leading to Corneal Perforation Selcuk Sizmaz, Aysel Pelit, Meltem Yagmur, Didem Arslan, Yonca Aydin Akova
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A 27 year-old man Two day history of redness in the right eye Corneal thinning involving the anterior stroma and adjacent conjunctival hyperemia, in the corneal limbus, at the 2- to 3-o’clock quadrant No sign of dry eye Topical ofloxacin and artificial tears prescribed
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Three days later, signs worsened –Thinning involved the posterior stroma –Patient declined surgery
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Two days later –Corneal perforation –İris prolapsed
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Corneal patch graft and amniotic membrane transplantation
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Ophthalmic and systemic evaluation No significant ocular history Oral aphthous lesions that had occurred once or twice a month for the previous 2 years Eight years history of lower back and buttock pain with morning stiffness for 30 minutes Arthralgia in the knee joints without swelling
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Arterial BP (mmHg) –130/80 right arm –100/70 left arm Weak pulse in left arm Colour Doppler USG: left subclavian artery narrowing MR angipgraphy: 4 cm- long diffuse stenosis in left subclavian artery Sacroiliac graphy: grade II-III sacroiliitis Pathergy test: (-) Erithrocyte sedimantation rate 35 mm/h C-reactive protein4.5 mg/L (↑) HBV(-) HCV(-) HIV(-) ANA(-) C-ANCA(-) HLA-B27(-) HLA-B51(-)
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Diagnosis: Behçet’s disease Oral aphthous lesions Ocular involvement Large vessel vasculitis Sacroiliitis
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Management: –Methylprednisolone, 32 mg/day, po; tapered –Azathioprine, 150 mg/day, po Prognosis (1 year follow-up): –No recurrence –Systemic symptoms improved
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Differential diagnosis Takayasu arteritis +Aorta and branches involved –No aphthous lesions –Sacroiliitis uncommon –Ocular invovement rare Polyarteritis nodosa +Peripheral ulcerative keratitis occurs –Predominantly females –Aneurisms in small-middle sized vessels –Constitutional symptoms
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