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      안면 마비와 난청으로 진단된 면역글로불린 G4 연관질환 동반 육아종성 다발 혈관염 1예 = A Case of Granulomatosis with Polyangiitis with IgG4-Related Disease Expressed by Facial Paralysis and Hearing Loss

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      https://www.riss.kr/link?id=A105981648

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      다국어 초록 (Multilingual Abstract)

      Granulomatosis with polyangiitis (GPA) and Immunoglobulin (Ig) G4-related disease (IgG4-RD) are rare diseases and early diagnosis and proper management are imperative to prevent multi-organ damage. The authors present a case of a 60 years old woman who had facial paralysis and hearing loss. Lt intact canal wall tympanomastoidectomy, Lt facial nerve decompression and ossiculoplasty with partial ossicular replacement prosthesis (PORP) was done. During operation, middle ear tissue was biopsied and GPA with IgG4-RD was diagnosed. After methyl prednisolone (MPD) pulse therapy and azathioprine therapy, the severity of paralysis was improved. We present this case because common otologic symptoms like facial palsy and hearing loss could be initial symptoms of rare systemic disease
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      Granulomatosis with polyangiitis (GPA) and Immunoglobulin (Ig) G4-related disease (IgG4-RD) are rare diseases and early diagnosis and proper management are imperative to prevent multi-organ damage. The authors present a case of a 60 years old woman wh...

      Granulomatosis with polyangiitis (GPA) and Immunoglobulin (Ig) G4-related disease (IgG4-RD) are rare diseases and early diagnosis and proper management are imperative to prevent multi-organ damage. The authors present a case of a 60 years old woman who had facial paralysis and hearing loss. Lt intact canal wall tympanomastoidectomy, Lt facial nerve decompression and ossiculoplasty with partial ossicular replacement prosthesis (PORP) was done. During operation, middle ear tissue was biopsied and GPA with IgG4-RD was diagnosed. After methyl prednisolone (MPD) pulse therapy and azathioprine therapy, the severity of paralysis was improved. We present this case because common otologic symptoms like facial palsy and hearing loss could be initial symptoms of rare systemic disease

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      참고문헌 (Reference)

      1 Gottschlich S, "Wegener’s granulomatosis in the head and neck region" 52 (52): 935-945, 2004

      2 De Groot K, "Standardized neurologic evaluation of 128 patients with Wegener granulomatosis" 58 : 1215-1221, 2001

      3 Khosroshahi A, "Rituximab for the treatment of IgG4-related disease : lessons from 10 consecutive patients" 91 : 57-, 2012

      4 Ebbo M, "Long-term efficacy and safety of rituximab in IgG4-related disease: Data from a French nationwide study of thirty-three patients" 12 (12): e0183844-, 2017

      5 Wallace ZS, "IgG4-Related Disease : Clinical and Laboratory Features in One Hundred Twenty-Five Patients" 67 (67): 2466-2475, 2015

      6 Falk RJ, "Granulomatosis with polyangiitis (Wegener’s):an alternative name for Wegener’s granulomatosis" 22 (22): 587-588, 2011

      7 Yates M, "EULAR/ERA-EDTA recommendations for the management of ANCA-associated vasculitis" 75 : 1583-, 2016

      8 Umehara H, "Comprehensive diagnostic criteria for IgG4-related disease, 2011" 22 : 21-30, 2012

      9 Danlos FX, "Antineutrophil cytoplasmic antibody-associated vasculitides and IgG4-related disease : a new overlap symdrome" 16 (16): 1036-1043, 2017

      10 Umehara H, "A novel clinical entity, IgG4-related disease (IgG4RD): general concept and details" 22 : 1-14, 2012

      1 Gottschlich S, "Wegener’s granulomatosis in the head and neck region" 52 (52): 935-945, 2004

      2 De Groot K, "Standardized neurologic evaluation of 128 patients with Wegener granulomatosis" 58 : 1215-1221, 2001

      3 Khosroshahi A, "Rituximab for the treatment of IgG4-related disease : lessons from 10 consecutive patients" 91 : 57-, 2012

      4 Ebbo M, "Long-term efficacy and safety of rituximab in IgG4-related disease: Data from a French nationwide study of thirty-three patients" 12 (12): e0183844-, 2017

      5 Wallace ZS, "IgG4-Related Disease : Clinical and Laboratory Features in One Hundred Twenty-Five Patients" 67 (67): 2466-2475, 2015

      6 Falk RJ, "Granulomatosis with polyangiitis (Wegener’s):an alternative name for Wegener’s granulomatosis" 22 (22): 587-588, 2011

      7 Yates M, "EULAR/ERA-EDTA recommendations for the management of ANCA-associated vasculitis" 75 : 1583-, 2016

      8 Umehara H, "Comprehensive diagnostic criteria for IgG4-related disease, 2011" 22 : 21-30, 2012

      9 Danlos FX, "Antineutrophil cytoplasmic antibody-associated vasculitides and IgG4-related disease : a new overlap symdrome" 16 (16): 1036-1043, 2017

      10 Umehara H, "A novel clinical entity, IgG4-related disease (IgG4RD): general concept and details" 22 : 1-14, 2012

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2022 평가예정 재인증평가 신청대상 (재인증)
      2019-01-01 평가 등재학술지 유지 (계속평가) KCI등재
      2016-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2015-01-01 평가 등재후보학술지 유지 (계속평가) KCI등재후보
      2013-01-01 평가 등재후보학술지 유지 (기타) KCI등재후보
      2011-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.06 0.06 0.05
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.05 0.06 0.176 0.04
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