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10.2147/IMCRJ.S89507

http://scihub22266oqcxt.onion/10.2147/IMCRJ.S89507
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C4581778!4581778!26425107
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suck abstract from ncbi


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pmid26425107      Int+Med+Case+Rep+J 2015 ; 8 (ä): 193-7
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  • Relapsing polychondritis with different types of ocular inflammations #MMPMID26425107
  • Furuya N; Oshitari T; Yotsukura J; Baba T; Yamamoto S
  • Int Med Case Rep J 2015[]; 8 (ä): 193-7 PMID26425107show ga
  • We were presented with two cases of relapsing polychondritis (RP) associated with different types of ocular inflammation. The first case was a 35-year-old man who had bilateral hyperemic conjunctiva and ocular pain, and was referred to Chiba University Hospital with a diagnosis of episcleritis refractory. He was treated with dexamethasone eye drops. He developed tinnitus, deafness in both ears, and left auriculitis. A left auricular biopsy showed an infiltration of lymphocytes surrounding the cartilage. He was diagnosed with RP and treated with 30 mg/day oral prednisolone. After tapering the prednisolone, the scleritis in both eyes improved. The second case was a 71-year-old man who was deaf in both ears and had bilateral scleritis. At the first visit to our hospital, his left eyelid and right auricula were reddish and swollen, and he reported some pain. He was treated with intravenous antibiotics, and the left orbital cellulitis quickly improved. However, he developed right scleritis and left gonitis. Magnetic resonance imaging showed bilateral posterior scleritis and right auricular perichondritis. Auricular biopsy showed an infiltration of lymphocytes into the periauricular tissue. He was diagnosed with RP, and 40 mg/day oral prednisolone was given and his symptoms improved. Although RP is rare, it is a life-threatening disease. Thus, ophthalmologists should consider RP in patients with both ocular and auricular inflammation.
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