Literature DB >> 21841333

A patient with myeloperoxidase antineutrophil cytoplasmic antibody-positive polyangiitis who developed sensorineural hearing loss and scleritis.

Takafumi Okura1, Ken-ichi Miyoshi, Masanori Jotoku, Daijiro Enomoto, Jun Irita, Tomoaki Nagao, Ryoji Ito, Jitsuo Higaki.   

Abstract

A 70-year-old woman was admitted to our hospital because of sudden hearing loss. She was treated with intratympanic dexamethasone, but her hearing impairment progressed. After admission, she developed scleritis of her left eye. Laboratory findings included elevated white blood cell count and C-reactive protein level, microhematuria, and proteinuria. Serology was positive for myeloperoxidase antineutrophil cytoplasmic antibody (MPO-ANCA), but negative for proteinase 3 (PR3)-ANCA. Renal biopsy revealed a single glomerulus with extensive glomerular tuft necrosis, indicating necrotizing vasculitis. She was diagnosed with MPO-ANCA-associated polyangiitis. ANCA-related polyangiitis should be considered in the differential diagnosis of sudden deafness or scleritis.

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Year:  2011        PMID: 21841333     DOI: 10.2169/internalmedicine.50.4953

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  1 in total

1.  AP-VAS 2012 case report: a case of myeloperoxidase antineutrophil cytoplasmic antibody-positive microscopic polyangiitis with rapidly progressive glomerulonephritis and hearing loss.

Authors:  Maki Tsukamoto; Seiichiro Shimizu; Megumi Koizumi; Nobuo Kitahara; Yoshihiro Ohtaki; Shigeyuki Aoki; Hiroshi Miyakawa
Journal:  CEN Case Rep       Date:  2013-01-30
  1 in total

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