1. Schaller JG. The history of pediatric rheumatology. Pediatr Res. 2005; 58:997–1007.
Article
2. Srinivasalu H, Riebschleger M. Medical education in pediatric rheumatology: unique challenges and opportunities. Clin Rheumatol. 2020; 39:643–50.
Article
3. Husserl FE, Shuler SE. Gold nephropathy in juvenile rheumatoid arthritis. Am J Dis Child. 1979; 133:50–2.
Article
4. Rovenska E, Kapeller K, Rossmann P. Gold nephropathy in rheumatoid arthritis and in juvenile chronic arthritis. Czech Med. 1979; 2:125–33.
5. Koseki Y, Terai C, Moriguchi M, Uesato M, Kamatani N. A prospective study of renal disease in patients with early rheumatoid arthritis. Ann Rheum Dis. 2001; 60:327–31.
Article
6. Deschenes G, Prieur AM, Hayem F, Broyer M, Gubler MC. Renal amyloidosis in juvenile chronic arthritis: evolution after chlorambucil treatment. Pediatr Nephrol. 1990; 4:463–9.
Article
7. Bilginer Y, Akpolat T, Ozen S. Renal amyloidosis in children. Pediatr Nephrol. 2011; 26:1215–27.
Article
8. Immonen K, Savolainen A, Kautiainen H, Hakala M. Longterm outcome of amyloidosis associated with juvenile idiopathic arthritis. J Rheumatol. 2008; 35:907–12.
9. David J, Vouyiouka O, Ansell BM, Hall A, Woo P. Amyloidosis in juvenile chronic arthritis: a morbidity and mortality study. Clin Exp Rheumatol. 1993; 11:85–90.
10. Schneider R, Passo MH. Juvenile rheumatoid arthritis. Rheum Dis Clin North Am. 2002; 28:503–30.
Article
11. Dhillon V, Woo P, Isenberg D. Amyloidosis in the rheumatic diseases. Ann Rheum Dis. 1989; 48:696–701.
Article
12. Chantarogh S, Vilaiyuk S, Tim-Aroon T, Worawichawong S. Clinical improvement of renal amyloidosis in a patient with systemic-onset juvenile idiopathic arthritis who received tocilizumab treatment: a case report and literature review. BMC Nephrol. 2017; 18:159.
Article
13. Gupta A, Bagri NK, Tripathy SK, Barwad A, Phulware RH, Hari P. Successful use of tocilizumab in amyloidosis secondary to systemic juvenile idiopathic arthritis. Rheumatol Int. 2020; 40:153–9.
Article
14. Okuda Y, Takasugi K. Successful use of a humanized anti-interleukin-6 receptor antibody, tocilizumab, to treat amyloid A amyloidosis complicating juvenile idiopathic arthritis. Arthritis Rheum. 2006; 54:2997–3000.
Article
15. Mielants H, Van den Bosch F. Extra-articular manifestations. Clin Exp Rheumatol. 2009; 27(4 Suppl 55):S56–61.
16. Adu D, Berisa F, Howie AJ, Emery P, Bacon PA, McConkey B, et al. Glomerulonephritis in rheumatoid arthritis. Br J Rheumatol. 1993; 32:1008–11.
Article
17. Bandin F, Merhenberger M, Modesto A, Brochard K, Decramer S. Steroid-responsive nephrotic syndrome in a child with juvenile idiopathic arthritis. Pediatr Nephrol. 2008; 23:651–4.
Article
18. Breedveld FC, Valentijn RM, Westedt ML, Weening JJ. Rapidly progressive glomerulonephritis with glomerular crescent formation in rheumatoid arthritis. Clin Rheumatol. 1985; 4:353–9.
Article
19. Helin HJ, Korpela MM, Mustonen JT, Pasternack AI. Renal biopsy findings and clinicopathologic correlations in rheumatoid arthritis. Arthritis Rheum. 1995; 38:242–7.
Article
20. Gedalia A, Mendez EA, Craver R, Vehaskari M, Espinoza LR. Renal involvement in juvenile rheumatoid arthritis: report of two cases. Clin Rheumatol. 2001; 20:153–6.
Article
21. Varma S. Juvenile rheumatoid arthritis with focal segmental glomerulosclerosis: a rare association. Pediatr Nephrol. 2010; 25:2189–90.
Article
22. Kari JA, Bamashmous H, Mahan JD. Steroid-sensitive nephrotic syndrome and juvenile idiopathic arthritis. Pediatr Nephrol. 2002; 17:975–6.
Article
23. Lipnick RN, Tsokos GC, Magilavy DB. Immune abnormalities in the pathogenesis of juvenile rheumatoid arthritis. Rheum Dis Clin North Am. 1991; 17:843–57.
Article
24. Foster BJ, Duffy CM, Sharma AK. Systemic juvenile rheumatoid arthritis complicated by two different renal lesions. Pediatr Nephrol. 1998; 12:113–6.
Article
25. Francois H, Mariette X. Renal involvement in primary Sjogren syndrome. Nat Rev Nephrol. 2016; 12:82–93.
26. Pessler F, Emery H, Dai L, Wu YM, Monash B, Cron RQ, et al. The spectrum of renal tubular acidosis in paediatric Sjogren syndrome. Rheumatology (Oxford). 2006; 45:85–91.
Article
27. Brito-Zeron P, Baldini C, Bootsma H, Bowman SJ, Jonsson R, Mariette X, et al. Sjogren syndrome. Nat Rev Dis Primers. 2016; 2:16047.
28. Tucker L, Ciurtin C. Sjogren syndrome and immunoglobulin-G4 disease. In : Petty RE, Laxer RM, Lindsley CB, Wedderburn LR, Mellins ED, Fuhlbrigge RC, editors. Textbook of pediatric rheumatology. 8th ed. Philadelphia: Elsevier;2021. p. 417–26.
29. Zhao J, Chen Q, Zhu Y, Zhao M, Liu J, Zhang Z, et al. Nephrological disorders and neurological involvement in pediatric primary Sjogren syndrome: a case report and review of literature. Pediatr Rheumatol Online J. 2020; 18:39.
Article
30. Aiyegbusi O, McGregor L, McGeoch L, Kipgen D, Geddes CC, Stevens KI. Renal disease in primary Sjogren’s syndrome. Rheumatol Ther. 2021; 8:63–80.
31. Katsifis GE, Rekka S, Moutsopoulos NM, Pillemer S, Wahl SM. Systemic and local interleukin-17 and linked cytokines associated with Sjogren’s syndrome immunopathogenesis. Am J Pathol. 2009; 175:1167–77.
32. Goules A, Geetha D, Arend LJ, Baer AN. Renal involvement in primary Sjogren’s syndrome: natural history and treatment outcome. Clin Exp Rheumatol. 2019; 37 Suppl 118:123–32.
33. Gu X, Su Z, Chen M, Xu Y, Wang Y. Acquired Gitelman syndrome in a primary Sjogren syndrome patient with a SLC12A3 heterozygous mutation: a case report and literature review. Nephrology (Carlton). 2017; 22:652–5.
34. Ren H, Wang WM, Chen XN, Zhang W, Pan XX, Wang XL, et al. Renal involvement and followup of 130 patients with primary Sjogren’s syndrome. J Rheumatol. 2008; 35:278–84.
35. Cohen EP, Bastani B, Cohen MR, Kolner S, Hemken P, Gluck SL. Absence of H(+)-ATPase in cortical collecting tubules of a patient with Sjogren’s syndrome and distal renal tubular acidosis. J Am Soc Nephrol. 1992; 3:264–71.
Article
36. Pedro-Botet J, Tomas S, Soriano JC, Coll J. Primary Sjogren’s syndrome associated with Bartter’s syndrome. Clin Exp Rheumatol. 1991; 9:210–2.
37. Oliva-Damaso N, Oliva-Damaso E, Payan J. Acute and chronic tubulointerstitial nephritis of rheumatic causes. Rheum Dis Clin North Am. 2018; 44:619–33.
Article
38. Jung SK, Park KH, Yim HE, Yoo KH, Hong YS, Lee JW, et al. Primary Sjogren’s syndrome with mesangial proliferative glomerulonephritis and IgA deposits in a child. Pediatr Nephrol. 2010; 25:567–8.
Article
39. Yoshida K, Suzuki J, Kume K, Suzuki S, Isome M, Kato K, et al. Sjogren’s syndrome with membranous glomerulonephritis detected by urine screening of schoolchildren. Acta Paediatr Jpn. 1996; 38:533–6.
40. Kagan M, Bervina N, Vorobyeva O, Wouters C, Levtchenko E. Pauci-immune crescentic glomerulonephritis complicating Sjogren’s syndrome in a 12-year-old girl. Pediatr Nephrol. 2011; 26:991–2.
Article
41. Dorfman RF, Berry GJ. Kikuchi’s histiocytic necrotizing lymphadenitis: an analysis of 108 cases with emphasis on differential diagnosis. Semin Diagn Pathol. 1988; 5:329–45.
42. Lin CY, Wu CH, Chen HA, Hsu CY, Wang LH, Su YJ. Long-term renal prognosis among patients with primary Sjogren’s syndrome and renal involvement: a nationwide matched cohort study. J Autoimmun. 2020; 113:102483.
43. Fragoulis GE, Zampeli E, Moutsopoulos HM. IgG4-related sialadenitis and Sjogren’s syndrome. Oral Dis. 2017; 23:152–6.
44. Boffa JJ, Esteve E, Buob D. Renal involvement in IgG4-related disease. Presse Med. 2020; 49:104017.
Article
45. Johnson JS, Saltzman AF, Treece AL, Cost NG. A case of IgG4-related renal pseudotumor in a child with history of Wilms tumor. Urol Case Rep. 2018; 21:107–9.
Article
46. Karim F, Loeffen J, Bramer W, Westenberg L, Verdijk R, van Hagen M, et al. IgG4-related disease: a systematic review of this unrecognized disease in pediatrics. Pediatr Rheumatol Online J. 2016; 14:18.
Article
47. Torok KS, Stevens AM. Juvenile systemic sclerosis. In : Petty RE, Laxer RM, Lindsley CB, Wedderburn LR, Mellins ED, Fuhlbrigge RC, editors. Textbook of pediatric rheumatology. 8th ed. Philadelphia: Elsevier;2021. p. 377–401.
48. Chrabaszcz M, Malyszko J, Sikora M, Alda-Malicka R, Stochmal A, Matuszkiewicz-Rowinska J, et al. Renal involvement in systemic sclerosis: an update. Kidney Blood Press Res. 2020; 45:532–48.
Article
49. Denton CP, Khanna D. Systemic sclerosis. Lancet. 2017; 390:1685–99.
Article
50. Herrick AL. Vascular function in systemic sclerosis. Curr Opin Rheumatol. 2000; 12:527–33.
Article
51. Steen VD. Scleroderma renal crisis. Rheum Dis Clin North Am. 2003; 29:315–33.
Article
52. Pamuk GE, Pamuk ON, Altiparmak MR, Tanverdi M, Uygun N, Yurdakul S. Secondary amyloidosis in progressive systemic sclerosis. Clin Rheumatol. 2001; 20:285–7.
Article
53. Papadopoulou C, McCann LJ. The vasculopathy of juvenile dermatomyositis. Front Pediatr. 2018; 6:284.
Article
54. Sangeetha G, Dhanabal D, Mouttou Prebagarane S, Janarthanan M. Juvenile dermatomyositis: a case of delayed recognition with unusual complication of nephrocalcinosis. BMJ Case Rep. 2021; 14:e241152.
Article
55. Couvrat-Desvergnes G, Masseau A, Benveniste O, Bruel A, Hervier B, Mussini JM, et al. The spectrum of renal involvement in patients with inflammatory myopathies. Medicine (Baltimore). 2014; 93:33–41.
Article
56. Mantoo MR, Tripathy SK, Phulware RH, Bagri NK, Hari P, Barwad A. Juvenile dermatomyositis with IgA nephropathy: case-based review. Rheumatol Int. 2019; 39:577–81.
Article
57. Wyatt RJ, Julian BA. IgA nephropathy. N Engl J Med. 2013; 368:2402–14.
Article
58. Stahl JL, Rutledge JC, Gordillo R. The unusual suspects: a curious case of acute kidney injury: answers. Pediatr Nephrol. 2019; 34:1213–5.
Article
59. Minoia F, Tibaldi J, Muratore V, Gallizzi R, Bracaglia C, Arduini A, et al. Thrombotic microangiopathy associated with macrophage activation syndrome: a multinational study of 23 patients. J Pediatr. 2021; 235:196–202.
Article