Renal histology in pauci-immune rapidly progressive glomerulonephritis: 8-year retrospective study.
dc.contributor.author | Minz, Ranjana W | |
dc.contributor.author | Chhabra, Seema | |
dc.contributor.author | Joshi, Kusum | |
dc.contributor.author | Rani, Lekha | |
dc.contributor.author | Sharma, Nidhi | |
dc.contributor.author | Sakhuja, Vinay | |
dc.contributor.author | Duggal, Rajan | |
dc.contributor.author | Pasricha, Neelam | |
dc.date.accessioned | 2012-10-16T04:02:37Z | |
dc.date.available | 2012-10-16T04:02:37Z | |
dc.date.issued | 2012-01 | |
dc.description.abstract | Context: The need to perform reporting of renal biopsies of antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitides in a more uniform manner required relook at our eight-year data. Aims: To document detailed renal histopathology of pauci-immune rapidly progressive glomerulonephritis (RPGN) and also to seek any significant differences in renal histology of C-ANCA-positive, P-ANCA-positive, and ANCA-negative patients. Materials and Methods: A detailed analysis of the histopathologic features of renal biopsies of 48 patients in whom a diagnosis of pauci-immune glomerulonephritis was concluded on renal biopsy and who presented clinically as rapidly progressive renal failure was done. Statistical Analysis Used: One-way ANOVA and Pearson Chi square tests. Results: Compared with ANCA +ve patients, the ANCA -ve patients were much younger (46.85 ± 16.12 years vs 34.28±15.94 years). No significant differences were found between renal lesions of C-ANCA, P-ANCA, and ANCA-negative patients, except for diffuse tubular atrophy which was more severe and more frequently present with P-ANCA positivity (P value=0.013). Conclusions: Pauci-immune RPGN (irrespective of ANCA status) is a relatively rare disorder in patients who are undergoing the renal biopsy at our institute, constituting 2% of all renal biopsies submitted. It is mandatory to have ANCA serology status during reporting of a kidney biopsy showing pauci-immune crescentic or necrotizing glomerulonephritis. Also, if a uniform reporting strategy is followed throughout the country, the studies from this vast country will be comparable. | en_US |
dc.identifier.citation | Minz Ranjana W, Chhabra Seema, Joshi Kusum, Rani Lekha, Sharma Nidhi, Sakhuja Vinay, Duggal Rajan, Pasricha Neelam. Renal histology in pauci-immune rapidly progressive glomerulonephritis: 8-year retrospective study. Indian Journal of Pathology & Microbiology. 2012 Jan-Mar 55(1): 28-32. | en_US |
dc.identifier.uri | https://imsear.searo.who.int/handle/123456789/142171 | |
dc.language.iso | en | en_US |
dc.source.uri | https://www.ijpmonline.org/article.asp?issn=0377-4929;year=2012;volume=55;issue=1;spage=28;epage=32;aulast=Minz | en_US |
dc.subject | Histology | en_US |
dc.subject | pauci-immune | en_US |
dc.subject | rapidly progressive glomerulonephritis | en_US |
dc.subject.mesh | Adolescent | |
dc.subject.mesh | Adult | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis --complications | |
dc.subject.mesh | Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis --pathology | |
dc.subject.mesh | Antibodies, Antineutrophil Cytoplasmic --blood | |
dc.subject.mesh | Biopsy | |
dc.subject.mesh | Child | |
dc.subject.mesh | Child, Preschool | |
dc.subject.mesh | Female | |
dc.subject.mesh | Glomerulonephritis --pathology | |
dc.subject.mesh | Histocytochemistry | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Immunohistochemistry | |
dc.subject.mesh | Infant | |
dc.subject.mesh | Kidney --pathology | |
dc.subject.mesh | Male | |
dc.subject.mesh | Microscopy | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Retrospective Studies | |
dc.title | Renal histology in pauci-immune rapidly progressive glomerulonephritis: 8-year retrospective study. | en_US |
dc.type | Article | en_US |