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      초점분절사구체경화증에서 발세포병증과 형태 변화 = Podocytopathy and Morphologic Changes in Focal Segmental Glomerulosclerosis

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      https://www.riss.kr/link?id=A101470763

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      다국어 초록 (Multilingual Abstract)

      Podocytopathy is glomerular lesions characterized by podocyte injury. It is observed in various glomerular diseases, but minimal change disease and focal segmental glomerulosclerosis (FSGS) are the prototypes. In this review, morphologic features of podocyte injury and subtypes of FSGS will be reviewed briefly. Effacement of podocyte foot processes is the most common feature of podocyte injury. As podocytic injury progresses, intracytoplasmic vacuoles, subpodocytic cyst, detachment of podocytes from the glomerular basement membrane and apoptosis develop. Glomerular capillary loops in epithelium-denuded area undergo capillary collapse. Synechia and hyalinosis may accompany this lesion. To manifest segmental sclerosis, podocyte loss above a threshold level may be required. Injured podocytes can injure neighboring intact podocytes, and thereby spread injury within the same lobule. FSGS can be categorized into five subtypes by morphologic characteristics; not otherwise specified (NOS), perihilar, cellular, tip, and collapsing types. Each subtype has been reported to show different clinical courses and associated conditions, but there are controversies on its significance. With recent progress in the discovery of genetic abnormalities causing FSGS and plasma permeability factors, we expect to unravel pathophysiology of FSGS and to understand histological sequences leading to FSGS in near future.
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      Podocytopathy is glomerular lesions characterized by podocyte injury. It is observed in various glomerular diseases, but minimal change disease and focal segmental glomerulosclerosis (FSGS) are the prototypes. In this review, morphologic features of p...

      Podocytopathy is glomerular lesions characterized by podocyte injury. It is observed in various glomerular diseases, but minimal change disease and focal segmental glomerulosclerosis (FSGS) are the prototypes. In this review, morphologic features of podocyte injury and subtypes of FSGS will be reviewed briefly. Effacement of podocyte foot processes is the most common feature of podocyte injury. As podocytic injury progresses, intracytoplasmic vacuoles, subpodocytic cyst, detachment of podocytes from the glomerular basement membrane and apoptosis develop. Glomerular capillary loops in epithelium-denuded area undergo capillary collapse. Synechia and hyalinosis may accompany this lesion. To manifest segmental sclerosis, podocyte loss above a threshold level may be required. Injured podocytes can injure neighboring intact podocytes, and thereby spread injury within the same lobule. FSGS can be categorized into five subtypes by morphologic characteristics; not otherwise specified (NOS), perihilar, cellular, tip, and collapsing types. Each subtype has been reported to show different clinical courses and associated conditions, but there are controversies on its significance. With recent progress in the discovery of genetic abnormalities causing FSGS and plasma permeability factors, we expect to unravel pathophysiology of FSGS and to understand histological sequences leading to FSGS in near future.

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      참고문헌 (Reference)

      1 정현주, "한국인 성인에서 국소분절사구체경화증의 아형에 따른 분석" 대한병리학회 44 (44): 589-596, 2010

      2 Ito H, "Twenty-seven children with focal segmental glomerulosclerosis: correlation between the segmental location of the glomerular lesions and prognosis" 22 : 9-14, 1984

      3 Neal CR, "Threedimensional reconstruction of glomeruli by electron microscopy reveals a distinct restrictive urinary subpodocyte space" 16 : 1223-1235, 2005

      4 D'Agati VD, "The spectrum of focal segmental glomerulosclerosis: new insights" 17 : 271-281, 2008

      5 Dijkman H, "The parietal epithelial cell is crucially involved in human idiopathic focal segmental glomerulosclerosis" 68 : 1562-1572, 2005

      6 Beaman M, "The glomerular tip lesion: a steroid responsive nephrotic syndrome" 27 : 217-221, 1987

      7 Howie AJ, "The glomerular tip lesion: a previously undescribed type of segmental glomerular abnormality" 142 : 205-220, 1984

      8 Barisoni L, "The dysregulated podocyte phenotype: a novel concept in the pathogenesis of collapsing idiopathic focal segmental glomerulosclerosis and HIV-associated nephropathy" 10 : 51-61, 1999

      9 Morita M, "The clinical significance of the glomerular location of segmental lesions in focal segmental glomerulosclerosis" 33 : 211-219, 1990

      10 Canaud G, "Recurrence of nephrotic syndrome after transplantation in a mixed population of children and adults: course of glomerular lesions and value of the Columbia classification of histological variants of focal and segmental glomerulosclerosis (FSGS)" 25 : 1321-1328, 2010

      1 정현주, "한국인 성인에서 국소분절사구체경화증의 아형에 따른 분석" 대한병리학회 44 (44): 589-596, 2010

      2 Ito H, "Twenty-seven children with focal segmental glomerulosclerosis: correlation between the segmental location of the glomerular lesions and prognosis" 22 : 9-14, 1984

      3 Neal CR, "Threedimensional reconstruction of glomeruli by electron microscopy reveals a distinct restrictive urinary subpodocyte space" 16 : 1223-1235, 2005

      4 D'Agati VD, "The spectrum of focal segmental glomerulosclerosis: new insights" 17 : 271-281, 2008

      5 Dijkman H, "The parietal epithelial cell is crucially involved in human idiopathic focal segmental glomerulosclerosis" 68 : 1562-1572, 2005

      6 Beaman M, "The glomerular tip lesion: a steroid responsive nephrotic syndrome" 27 : 217-221, 1987

      7 Howie AJ, "The glomerular tip lesion: a previously undescribed type of segmental glomerular abnormality" 142 : 205-220, 1984

      8 Barisoni L, "The dysregulated podocyte phenotype: a novel concept in the pathogenesis of collapsing idiopathic focal segmental glomerulosclerosis and HIV-associated nephropathy" 10 : 51-61, 1999

      9 Morita M, "The clinical significance of the glomerular location of segmental lesions in focal segmental glomerulosclerosis" 33 : 211-219, 1990

      10 Canaud G, "Recurrence of nephrotic syndrome after transplantation in a mixed population of children and adults: course of glomerular lesions and value of the Columbia classification of histological variants of focal and segmental glomerulosclerosis (FSGS)" 25 : 1321-1328, 2010

      11 Schwartz MM, "Primary focal segmental glomerular sclerosis in adults: prognostic value of histologic variants" 25 : 845-852, 1995

      12 Bariety J, "Podocytes undergo phenotypic changes and express macrophagic-associated markers in idiopathic collapsing glomerulopathy" 53 : 918-928, 1998

      13 Matsusaka T, "Podocyte injury damages other podocytes" 22 : 1275-1285, 2011

      14 Wharram BL, "Podocyte depletion causes glomerulosclerosis: diphtheria toxin-induced podocyte depletion in rats expressing human diphtheria toxin receptor transgene" 16 : 2941-2952, 2005

      15 Deegens JK, "Pathological variants of focal segmental glomerulosclerosis in an adult Dutch population--epidemiology and outcome" 23 : 186-192, 2008

      16 D'Agati VD, "Pathologic classification of focal segmental glomerulosclerosis: a working proposal" 43 : 368-382, 2004

      17 Kambham N, "Obesity-related glomerulopathy: an emerging epidemic" 59 : 1498-1509, 2001

      18 Weiss MA, "Nephrotic syndrome, progressive irreversible renal failure, and glomerular "collapse": a new clinicopathologic entity?" 7 : 20-28, 1986

      19 Valeri A, "Idiopathic collapsing focal segmental glomerulosclerosis: a clinicopathologic study" 50 : 1734-1746, 1996

      20 Cohen AH, "Glomerular podocyte degeneration in human renal disease: an ultrastructural study" 37 : 30-42, 1977

      21 Schwartz MM, "Focal segmental glomerular sclerosis: the cellular lesion" 28 : 968-974, 1985

      22 Grishman E, "Focal glomerular sclerosis in nephrotic patients: an electron microscopic study of glomerular podocytes" 7 : 111-122, 1975

      23 Howie AJ, "Evolution of nephrotic-associated focal segmental glomerulosclerosis and relation to the glomerular tip lesion" 67 : 987-1001, 2005

      24 Meyrier AY, "Collapsing glomerulopathy: expanding interest in a shrinking tuft" 33 : 801-803, 1999

      25 Grcevska L, "Collapsing glomerulopathy: clinical characteristics and follow-up" 33 : 652-657, 1999

      26 Detwiler RK, "Collapsing glomerulopathy: a clinically and pathologically distinctvariant of focal segmental glomerulosclerosis" 45 : 1416-1424, 1994

      27 Santin S, "Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome" 6 : 1139-1148, 2011

      28 Thomas DB, "Clinical and pathologic characteristics of focal segmental glomerulosclerosis pathologic variants" 69 : 920-926, 2006

      29 Wei C, "Circulating urokinase receptor as a cause of focal segmental glomerulosclerosis" 17 : 952-960, 2011

      30 Stokes MB, "Cellular focal segmental glomerulosclerosis: Clinical and pathologic features" 70 : 1783-1792, 2006

      31 Nagata M, "Cell cycle regulation and differentiation in the huma podocyte lineage" 153 : 1511-1520, 1998

      32 Shimamura T, "A collapsing form of glomerulopathy" 45 : 520-523, 1995

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      학술지 이력
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      2024 평가예정 계속평가 신청대상 (계속평가)
      2022-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
      2021-12-01 평가 등재후보 탈락 (계속평가)
      2019-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
      2018-12-01 평가 등재후보 탈락 (계속평가)
      2017-12-01 평가 등재후보로 하락 (계속평가) KCI등재후보
      2016-01-12 학술지명변경 한글명 : 대한소아신장학회지 -> Childhood Kidney Diseases
      외국어명 : Journal of the Korean Society of Pediatric Nephrology -> Childhood Kidney diseases
      KCI등재
      2013-01-01 평가 등재 1차 FAIL (등재유지) KCI등재
      2010-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2009-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2008-01-01 평가 신청제한 (등재후보1차) KCI등재
      2007-01-01 평가 등재후보 1차 FAIL (등재후보2차) KCI등재후보
      2006-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2004-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.12 0.12 0.13
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.11 0.11 0.332 0
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