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      KCI등재후보

      다운증후군 환자에서 병발한 재발성 다발연골염과 괴저성 농피증 = A case of relapsing polychondritis and pyoderma gangrenosum in a patient with Down`s syndrome

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      https://www.riss.kr/link?id=A76373499

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      다국어 초록 (Multilingual Abstract)

      Relapsing polychondritis (RP) is a rare multisystem disorder of unknown etiology that affects cartilaginous tissues, such as the auricular, nasal, and laryngotracheal cartilages. It may be accompanied by a wide spectrum of skin lesions, including erythema nodosum, erythema multiforme, and panniculitis. Pyoderma gangrenosum is a rare chronic cutaneous disease that usually presents as a painful nodule or pustule and progressively forms an enlarging ulcer. It may be associated with inflammatory bowel disease, rheumatoid arthritis, systemic lupus erythromatosus, leukemia, and myeloproliferative disorders. Pyoderma gangrenosum is rarely associated with RP. RP and pyoderma gangrenosum have been reported in a patient with myelodysplastic syndrome (MDS), and the appearance of skin lesions in MDS may herald its progression to acute myeloid leukemia. Here, we report the first case of RP coexisting with pyoderma gangrenosum in a patient with Down`s syndrome. (Korean J Med 76:632-636, 2009)
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      Relapsing polychondritis (RP) is a rare multisystem disorder of unknown etiology that affects cartilaginous tissues, such as the auricular, nasal, and laryngotracheal cartilages. It may be accompanied by a wide spectrum of skin lesions, including eryt...

      Relapsing polychondritis (RP) is a rare multisystem disorder of unknown etiology that affects cartilaginous tissues, such as the auricular, nasal, and laryngotracheal cartilages. It may be accompanied by a wide spectrum of skin lesions, including erythema nodosum, erythema multiforme, and panniculitis. Pyoderma gangrenosum is a rare chronic cutaneous disease that usually presents as a painful nodule or pustule and progressively forms an enlarging ulcer. It may be associated with inflammatory bowel disease, rheumatoid arthritis, systemic lupus erythromatosus, leukemia, and myeloproliferative disorders. Pyoderma gangrenosum is rarely associated with RP. RP and pyoderma gangrenosum have been reported in a patient with myelodysplastic syndrome (MDS), and the appearance of skin lesions in MDS may herald its progression to acute myeloid leukemia. Here, we report the first case of RP coexisting with pyoderma gangrenosum in a patient with Down`s syndrome. (Korean J Med 76:632-636, 2009)

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      참고문헌 (Reference)

      1 Michet CJ Jr, "Relapsing polychondritis: survival and predictive role of early disease manifestations" 104 : 74-78, 1986

      2 Damiani JM, "Relapsing polychondritis: report of ten cases" 89 : 929-946, 1979

      3 McAdam LP, "Relapsing polychondritis: prospective study of 23 patients and a review of the literature" 55 : 193-215, 1976

      4 Letko E, "Relapsing polychondritis: a clinical review" 31 : 384-395, 2002

      5 Myers B, "Relapsing polychondritis and myelodysplasia: a report of two cases and review of the current literature" 22 : 45-48, 2000

      6 Wright MJ, "Relapsing polychondritis and myelodysplasia" 12 : 1704-1707, 1997

      7 Silva J, "Relapsing polychondritis and Reiter’s syndrome" 18 : 908-910, 1991

      8 Seok JH, "Pyodermal gangrenosum in ulcerative colitis" 19 : 300-305, 199

      9 Hughes JR, "Pyoderma gangrenosum in a patient with rheumatoid arthritis responding to treatment with cyclosporine A" 33 : 680-681, 1994

      10 Callen JP, "Pyoderma gangrenosum" 351 : 581-585, 1998

      1 Michet CJ Jr, "Relapsing polychondritis: survival and predictive role of early disease manifestations" 104 : 74-78, 1986

      2 Damiani JM, "Relapsing polychondritis: report of ten cases" 89 : 929-946, 1979

      3 McAdam LP, "Relapsing polychondritis: prospective study of 23 patients and a review of the literature" 55 : 193-215, 1976

      4 Letko E, "Relapsing polychondritis: a clinical review" 31 : 384-395, 2002

      5 Myers B, "Relapsing polychondritis and myelodysplasia: a report of two cases and review of the current literature" 22 : 45-48, 2000

      6 Wright MJ, "Relapsing polychondritis and myelodysplasia" 12 : 1704-1707, 1997

      7 Silva J, "Relapsing polychondritis and Reiter’s syndrome" 18 : 908-910, 1991

      8 Seok JH, "Pyodermal gangrenosum in ulcerative colitis" 19 : 300-305, 199

      9 Hughes JR, "Pyoderma gangrenosum in a patient with rheumatoid arthritis responding to treatment with cyclosporine A" 33 : 680-681, 1994

      10 Callen JP, "Pyoderma gangrenosum" 351 : 581-585, 1998

      11 Jaksch-Wartenhorst R, "Polychondropathia" 6 : 93-100, 1923

      12 Avivi, "Myelodysplastic syndrome and associated skin lesion: a review of the literature" 23 : 323-330, 1999

      13 Whitlock JA, "Down syndrome and acute lymphoblastic leukaemia" 135 : 595-602, 2006

      14 Nisar M, "Cyclosporin A in the treatment of rheumatoid associated pyoderma gangrenosum" 34 : 182-, 1995

      15 Frances C, "Cutaneous manifestations of Takayasu arteritis: a retrospective study of 80 cases" 181 : 266-272, 1990

      16 Goldacre MJ, "Cancers and immune related diseases associated with Down’s syndrome: a record linkage study" 89 : 1014-1017, 2004

      17 Cho HL, "A case of pyoderma gangrenosum associated with inactive ulcerative colitis" 18 : 597-603, 1998

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 계속평가 신청대상 (계속평가)
      2021-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
      2018-12-01 평가 등재후보 탈락 (계속평가)
      2017-12-01 평가 등재후보로 하락 (계속평가) KCI등재후보
      2013-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-05-15 학술지명변경 외국어명 : Korean Journal of Medicine -> The Korean Journal of Medicine KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2003-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2002-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2000-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.1 0.1 0.1
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.11 0.1 0.259 0.02
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