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Section 4 - Vascular Diseases

Published online by Cambridge University Press:  10 August 2023

Edited by
Helen Liapis
Helen Liapis
Affiliation:
Ludwig Maximilian University, Nephrology Center, Munich, Adjunct Professor and Washington University St Louis, Department of Pathology and Immunology, Retired Professor
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Pediatric Nephropathology & Childhood Kidney Tumors , pp. 213 - 230
Publisher: Cambridge University Press
Print publication year: 2023

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References

Mohammad, A. J., Jacobsson, L. T., Mahr, A. D., et al. Prevalence of Wegener’s granulomatosis, microscopic polyangiitis, polyarteritis nodosa and Churg-Strauss syndrome within a defined population in southern Sweden. Rheumatology 2007; 46: 1329–37.Google Scholar
Watts, R. A., Mahr, A., Mohammad, A. J., et al. Classification, epidemiology and clinical subgrouping of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis. Nephrol Dial Transplant. 2015; 30: 14–22.CrossRefGoogle ScholarPubMed
Berti, A., Cornec, D., Crowson, C. S., et al. The epidemiology of antineutrophil cytoplasmic autoantibody-associated vasculitis in Olmsted County, Minnesota: A twenty-year US population-based study. Arthritis Rheumatol. 2017; 69: 2338–50.Google Scholar
Li, J., Cui, Z., Long, J. Y., et al. The frequency of ANCA-associated vasculitis in a national database of hospitalized patients in China. Arthritis Res Ther. 2018; 20: 226.Google Scholar
Canney, M., O’Hara, P. V., McEvoy, C. M., et al. Spatial and temporal clustering of anti-glomerular basement membrane disease. Clin J Am Soc Nephrol. 2016; 11: 1392–9.Google Scholar
Ma, R., Cui, Z., Hu, S. Y., et al. The alternative pathway of complement activation may be involved in the renal damage of human anti-glomerular basement membrane disease. PLoS ONE 2014; 21: 9.Google Scholar
Sethi, S., Zand, L., De Vriese, A. S., et al. Complement activation in pauci-immune necrotizing and crescentic glomerulonephritis: Results of a proteomic analysis. Nephrol Dial Transplant. 2017; 32: 139–45.Google Scholar
Furuta, S., Jayne, D. R.. Antineutrophil cytoplasm antibody-associated vasculitis: Recent developments. Kidney Int. 2013; 84: 244–9.CrossRefGoogle ScholarPubMed
Savage, C. O., Pusey, C. D., Bowman, C., et al. Antiglomerular basement membrane antibody mediated disease in the British Isles 1980-4. Br Med J. 1986; 292: 301–4.Google Scholar
Cui, Z., Zhao, J., Jia, X. Y., et al. Anti-glomerular basement membrane disease: Outcomes of different therapeutic regimens in a large single-center Chinese cohort study. Medicine. 2011; 90: 303–11.CrossRefGoogle Scholar
Berden, A. E., Ferrario, F., Hagen, E. C., et al. Histopathologic classification of ANCA-associated glomerulonephritis. J Am Soc Nephrol. 2010; 21: 1628–36.Google Scholar
Brix, S. R., Noriega, M., Tennstedt, P., et al. Development and validation of a renal risk score in ANCA-associated glomerulonephritis. Kidney Int. 2018; 94: 1177–88.Google Scholar
Jones, R. B., Tervaert, J. W., Hauser, T., et al. Rituximab versus cyclophosphamide in ANCA-associated renal vasculitis. N Engl J Med. 2010; 363: 211–20.Google Scholar
Stone, J. H., Merkel, P. A., Spiera, R., et al. Rituximab versus cyclophosphamide for ANCA-associated vasculitis. N Engl J Med. 2010; 363: 221–32.Google Scholar
Yates, M., Watts, R. A., Bajema, I. M., et al. EULAR/ERA-EDTA recommendations for the management of ANCA-associated vasculitis. Ann Rheum Dis. 2016; 75: 1583–94.Google Scholar
Walsh, M., Merkel, P. A., Peh, C. A., et al. Plasma exchange and glucocorticoids in severe ANCA-associated vasculitis. N Engl J Med. 2020; 382: 622–31.CrossRefGoogle ScholarPubMed
Jayne, D. R. W., Merkel, P. A., Schall, T. J., et al. Avacopan for the treatment of ANCA-associated vasculitis. N Engl J Med. 2021; 384: 599–609.Google Scholar
Soveri, I., Mölne, J., Uhlin, F., et al. The IgG-degrading enzyme of Streptococcus pyogenes causes rapid clearance of anti-glomerular basement membrane antibodies in patients with refractory anti-glomerular basement membrane disease. Kidney Int. 2019; 96: 1234–8.Google Scholar
Zipfel, P. F., Wiech, T., Rudnick, R., et al. Complement inhibitors in clinical trials for glomerular diseases. Front Immunol. 2019; 10: 2166.CrossRefGoogle ScholarPubMed
Gavriilaki, E., Anagnostopoulos, A., Mastellos, D. C.. Complement in thrombotic microangiopathies: Unraveling Ariadne’s thread in to the labyrinth of complement therapeutics. Front Immunol. 2019; 10: 337.CrossRefGoogle Scholar
Ardissino, G., Salardi, S., Colombo, E., et al. Epidemiology of haemolytic uremic syndrome in children. Data from the North Italian HUS network. Eur J Pediatr. 2016; 175: 465–73.Google Scholar
Nester, C. M., Thomas, C. P.. Atypical hemolytic uremic syndrome: What is it, how is it diagnosed, and how is it treated? Hematology Am Soc Hematol Educ Program. 2012; 2012: 617–25.CrossRefGoogle Scholar
Elhadad, S., Chapin, J., Copertino, D., et al. MASP2 levels are elevated in thrombotic microangiopathies: Association with microvascular endothelial cell injury and suppression by anti-MASP2 antibody narsoplimab. Clin Exp Immunol. 2021; 203: 96–104.CrossRefGoogle ScholarPubMed
Coppo, P., Bubenheim, M., Azoulay, E., et al. A regimen with caplacizumab, immunosuppression, and plasma exchange prevents unfavorable outcomes in immune-mediated TTP. Blood. 2021; 137: 733–42.CrossRefGoogle ScholarPubMed
Brocklebank, V., Wood, K. M., Kavanagh, D.. Thrombotic microangiopathy and the kidney. Clin J Am Soc Nephrol. 2018; 13: 300–17.CrossRefGoogle ScholarPubMed
Conway, E. M., Pryzdia, E. L. G.. Is the COVID-19 thrombotic catastrophe complement-connected? J Thromb Haemost. 2020; 18: 2812–22.CrossRefGoogle ScholarPubMed
Cines, D. B., Bussel, J. B.. SARS-CoV-2 vaccine-induced immune thrombotic thrombocytopenia. N Engl J Med. 2021; 384: 2254–6.Google Scholar
Holz, J. B.. The TITAN trial--assessing the efficacy and safety of an anti-von Willebrand factor nanobody in patients with acquired thrombotic thrombocytopenic purpura. Transfus Apher Sci. 2012; 46: 343–6.Google Scholar
Rao, G.. Diagnosis, epidemiology, and management of hypertension in children. Pediatrics. 2016; 138: 3616.CrossRefGoogle ScholarPubMed
Mills, K. T., Bundy, J. D., Tanika, N., et al. Global disparities of hypertension prevalence and control: A systematic analysis of population-based studies from 90 countries. Circulation 2016; 134: 441–50.Google Scholar
Lewington, S., Clarke, R., Qizilbash, N., et al.; Prospective Studies Collaboration. Age-specific relevance of usual blood pressure to vascular mortality: A meta-analysis of individual data for one million adults in 61 prospective studies. Lancet. 2002; 360: 1903–13.Google ScholarPubMed
Whelton PK, Carey RM, Aronow WS, et al. 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA Guideline for the Prevention, Detection, Evaluation, and Management of High Blood Pressure in Adults: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. J Am Coll Cardiol. 2018 May 15;71(19):e127–e248. doi: 10.1016/j.jacc.2017.11.006. Epub 2017 Nov 13. Erratum in: J Am Coll Cardiol. 2018 May 15;71 (19):2275–2279. PMID: 29146535.Google Scholar
Patel, P. A., Cahill, A. M.. Renovascular hypertension in children. CVIR Endovasc. 2021; 4: 10.CrossRefGoogle ScholarPubMed
Riedlinger, W. F., Kissane, J. M., Gibfried, M., Liapis, H.. Congenital bilateral renal arteriovenous malformation: An unrecognized cause of renal failure. Pediatr Dev Pathol. 2004; 7(3): 285–9.Google Scholar
Watanabe, T.. Kidney and urinary tract involvement in kawasaki disease. Int J Pediatr. 2013; 2013: 831834.CrossRefGoogle ScholarPubMed
Whelton PK, Carey RM, Aronow WS, etal ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA Guideline for the Prevention, Detection, Evaluation, and Management of High Blood Pressure in Adults: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. J Am Coll Cardiol. 2018;71(19):e127–e248.Google Scholar
Calatroni M, Consonni F, Allinovi M, etal. Prognostic Factors and Long-Term Outcome with ANCA-Associated Kidney Vasculitis in Childhood. Clin J Am Soc Nephrol. 2021;16(7):1043–51.Google Scholar

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  • Vascular Diseases
  • Edited by Helen Liapis, Ludwig Maximilian University, Nephrology Center, Munich, Adjunct Professor and Washington University St Louis, Department of Pathology and Immunology, Retired Professor
  • Book: Pediatric Nephropathology & Childhood Kidney Tumors
  • Online publication: 10 August 2023
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  • Vascular Diseases
  • Edited by Helen Liapis, Ludwig Maximilian University, Nephrology Center, Munich, Adjunct Professor and Washington University St Louis, Department of Pathology and Immunology, Retired Professor
  • Book: Pediatric Nephropathology & Childhood Kidney Tumors
  • Online publication: 10 August 2023
Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • Vascular Diseases
  • Edited by Helen Liapis, Ludwig Maximilian University, Nephrology Center, Munich, Adjunct Professor and Washington University St Louis, Department of Pathology and Immunology, Retired Professor
  • Book: Pediatric Nephropathology & Childhood Kidney Tumors
  • Online publication: 10 August 2023
Available formats
×