| [1] |
SCHALLER J, BECKWITH B, WEDGWOOD RJ. Hepatic involvement in juvenile rheumatoid arthritis[J]. 1970, 77( 2): 203- 210. DOI: 10.1016/s0022-3476(70)80324-9.
|
| [2] |
GIRALDO WAS, MORATILLA AB, CAPARRÓS AM, et al. Nodular regenerative hyperplasia of the liver as a complication of long-standing systemic-onset juvenile idiopathic arthritis[J]. Reumatol Clin, 2014, 10( 3): 194- 195. DOI: 10.1016/j.reuma.2013.09.001.
|
| [3] |
CANNA S, FRANKOVICH J, HIGGINS G, et al. Acute hepatitis in three patients with systemic juvenile idiopathic arthritis taking interleukin-1 receptor antagonist[J]. Pediatr Rheumatol Online J, 2009, 7: 21. DOI: 10.1186/1546-0096-7-21.
|
| [4] |
RUPERTO N, BRUNNER HI, QUARTIER P, et al. Two randomized trials of canakinumab in systemic juvenile idiopathic arthritis[J]. N Engl J Med, 2012, 367( 25): 2396- 2406. DOI: 10.1056/NEJMoa1205099.
|
| [5] |
GENOVESE MC, KREMER JM, van VOLLENHOVEN RF, et al. Transaminase levels and hepatic events during tocilizumab treatment: Pooled analysis of long-term clinical trial safety data in rheumatoid arthritis[J]. Arthritis Rheumatol, 2017, 69( 9): 1751- 1761. DOI: 10.1002/art.40176.
|
| [6] |
MINOIA F, DAVÌ S, HORNE A, et al. Clinical features, treatment, and outcome of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis: A multinational, multicenter study of 362 patients[J]. Arthritis Rheumatol, 2014, 66( 11): 3160- 3169. DOI: 10.1002/art.38802.
|
| [7] |
FAUTREL B, MITROVIC S, DE MATTEIS A, et al. EULAR/PReS recommendations for the diagnosis and management of Still’s disease, comprising systemic juvenile idiopathic arthritis and adult-onset Still’s disease[J]. Ann Rheum Dis, 2024, 83( 12): 1614- 1627. DOI: 10.1136/ard-2024-225851.
|
| [8] |
IRVING KS, SEN D, TAHIR H, et al. A comparison of autoimmune liver disease in juvenile and adult populations with systemic lupus erythematosus-a retrospective review of cases[J]. Rheumatology(Oxford), 2007, 46( 7): 1171- 1173. DOI: 10.1093/rheumatology/kem108.
|
| [9] |
TAKAHASHI A, ABE K, SAITO R, et al. Liver dysfunction in patients with systemic lupus erythematosus[J]. Intern Med, 2013, 52( 13): 1461- 1465. DOI: 10.2169/internalmedicine.52.9458.
|
| [10] |
TAHERNIA L, ALIMADADI H, TAHGHIGHI F, et al. Frequency and type of hepatic and gastrointestinal involvement in juvenile systemic lupus erythematosus[J]. Autoimmune Dis, 2017, 2017: 8097273. DOI: 10.1155/2017/8097273.
|
| [11] |
PIGA M, VACCA A, PORRU G, et al. Liver involvement in systemic lupus erythematosus: Incidence, clinical course and outcome of lupus hepatitis[J]. Clin Exp Rheumatol, 2010, 28( 4): 504- 510.
|
| [12] |
TRAPANI S, RUBINO C, SIMONINI G, et al. Gastrointestinal and hepatic involvement in paediatric systemic lupus erythematosus[J]. Clin Exp Rheumatol, 2021, 39( 4): 899- 906. DOI: 10.55563/clinexprheumatol/oebrcq.
|
| [13] |
EL-SHABRAWI MH, FARRAG MI. Hepatic manifestations in juvenile systemic lupus erythematosus[J]. Recent Pat Inflamm Allergy Drug Discov, 2014, 8( 1): 36- 40. DOI: 10.2174/1872213x07666131229110501.
|
| [14] |
AFZAL W, HAGHI M, HASNI SA, et al. Lupus hepatitis, more than just elevated liver enzymes[J]. Scand J Rheumatol, 2020, 49( 6): 427- 433. DOI: 10.1080/03009742.2020.1744712.
|
| [15] |
ADIGA A, NUGENT K. Lupus hepatitis and autoimmune hepatitis(lupoid hepatitis)[J]. Am J Med Sci, 2017, 353( 4): 329- 335. DOI: 10.1016/j.amjms.2016.10.014.
|
| [16] |
DEEN MJ, PORTA G, FIOROT FJ, et al. Autoimmune hepatitis and juvenile systemic lupus erythematosus[J]. Lupus, 2009, 18( 8): 747- 751. DOI: 10.1177/0961203308100559.
|
| [17] |
BALBI VA, MONTENEGRO B, PITTA AC, et al. Autoimmune hepatitis in 847 childhood-onset systemic lupus erythematosus population: A multicentric cohort study[J]. Adv Rheumatol, 2018, 58( 1): 43. DOI: 10.1186/s42358-018-0043-7.
|
| [18] |
PAWŁOWSKA J, NAORNIAKOWSKA M, LIBER A. Liver involvement in children with collagen vascular diseases[J]. Clin Exp Hepatol, 2015, 1( 3): 117- 119. DOI: 10.5114/ceh.2015.55569.
|
| [19] |
GRYKA-MARTON M, SZUKIEWICZ D, TELIGA-CZAJKOWSKA J, et al. An overview of neonatal lupus with anti-ro characteristics[J]. Int J Mol Sci, 2021, 22( 17): 9281. DOI: 10.3390/ijms22179281.
|
| [20] |
DERDULSKA JM, RUDNICKA L, SZYKUT-BADACZEWSKA A, et al. Neonatal lupus erythematosus-practical guidelines[J]. J Perinat Med, 2021, 49( 5): 529- 538. DOI: 10.1515/jpm-2020-0543.
|
| [21] |
RUSSO RA, KATSICAS MM, DÁVILA M, et al. Cholestasis in juvenile dermatomyositis: Report of three cases[J]. Arthritis Rheum, 2001, 44( 5): 1139- 1142.
|
| [22] |
KINKOR M, HAMEED S, KATS A, et al. 14-month-old female with anti-MDA5 juvenile dermatomyositis complicated by liver disease: A case report[J]. Pediatr Rheumatol Online J, 2024, 22( 1): 86. DOI: 10.1186/s12969-024-01021-y.
|
| [23] |
YI BY, MARRS J, SCHENKER R, et al. Elevated liver enzymes: Unusual presentation of anti-MDA5 antibody-associated juvenile dermatomyositis[J]. Clin Exp Rheumatol, 2024, 42( 2): 456- 457. DOI: 10.55563/clinexprheumatol/25znui.
|
| [24] |
RAMOS-CASALS M, ACAR-DENIZLI N, VISSINK A, et al. Childhood-onset of primary Sjögren’s syndrome: Phenotypic characterization at diagnosis of 158 children[J]. Rheumatology(Oxford), 2021, 60( 10): 4558- 4567. DOI: 10.1093/rheumatology/keab032.
|
| [25] |
GONG YN, LIU HM, LI GM, et al. Childhood-onset primary Sjögren’s syndrome in a tertiary center in China: Clinical features and outcome[J]. Pediatr Rheumatol Online J, 2023, 21( 1): 11. DOI: 10.1186/s12969-022-00779-3.
|
| [26] |
MARINO A, ROMANO M, GIANI T, et al. Childhood Sjogren’s syndrome: An Italian case series and a literature review-based cohort[J]. Semin Arthritis Rheum, 2021, 51( 4): 903- 910. DOI: 10.1016/j.semarthrit.2020.11.004.
|
| [27] |
KASHIWAGI Y, HATSUSHIKA T, TSUTSUMI N, et al. Gastrointestinal and liver lesions in primary childhood Sjögren syndrome[J]. Clin Rheumatol, 2017, 36( 6): 1433- 1435. DOI: 10.1007/s10067-017-3599-4.
|
| [28] |
GEBRESELASSIE A, ADULI F, HOWELL CD. Rheumatologic diseases and the liver[J]. Clin Liver Dis, 2019, 23( 2): 247- 261. DOI: 10.1016/j.cld.2018.12.007.
|
| [29] |
CHAO HC, KONG MS, LIN SJ. Hepatobiliary involvement of Henoch-Schönlein purpura in children[J]. Acta Paediatr Taiwan, 2000, 41( 2): 63- 68.
|
| [30] |
GATSELIS NK, STEFOS A, GIOTI C, et al. Primary biliary cirrhosis and Henoch-Schonlein purpura: Report of two cases and review of the literature[J]. Liver Int, 2007, 27( 2): 280- 283. DOI: 10.1111/j.1478-3231.2006.01402.x.
|
| [31] |
REN YF, ZHANG CX, XU XQ, et al. A case report of atypical Kawasaki disease presented with severe elevated transaminases and literature review[J]. BMC Infect Dis, 2021, 21( 1): 415. DOI: 10.1186/s12879-021-06101-y.
|
| [32] |
MORITA A, IMAGAWA K, ISHIODORI T, et al. Kawasaki disease with dilatation of the common bile duct: A case report and review of literature[J]. Int J Rheum Dis, 2021, 24( 10): 1325- 1330. DOI: 10.1111/1756-185X.14208.
|
| [33] |
PRATAP K, GARDNER LS, GILLIS D, et al. Hepatic predominant presentation of Kawasaki disease in adolescence case report and review of literature[J]. BMC Gastroenterol, 2020, 20( 1): 352. DOI: 10.1186/s12876-020-01461-2.
|
| [34] |
UNAL F, CAKIR M, BARAN M, et al. Liver involvement in children with familial Mediterranean fever[J]. Dig Liver Dis, 2012, 44( 8): 689- 693. DOI: 10.1016/j.dld.2012.01.003.
|
| [35] |
BAYRAMOGLU Z, AKYOL SARI ZN, KOKER O, et al. Shear wave elastography evaluation of liver, pancreas, spleen and kidneys in patients with familial mediterranean fever and amyloidosis[J]. Br J Radiol, 2021, 94( 1128): 20210237. DOI: 10.1259/bjr.20210237.
|
| [36] |
FRAISSE T, SAVEY L, HENTGEN V, et al. Non-amyloid liver involvement in familial Mediterranean fever: A systematic literature review[J]. Liver Int, 2020, 40( 6): 1269- 1277. DOI: 10.1111/liv.14445.
|
| [37] |
AOKI M, IZAWA K, TANAKA T, et al. Case report: A pediatric case of familial Mediterranean fever concurrent with autoimmune hepatitis[J]. Front Immunol, 2022, 13: 917398. DOI: 10.3389/fimmu.2022.917398.
|
| [38] |
WANG W, WANG W, ZOU LP, et al. Clinical characteristics of 25 patients with type I interferonopathies[J]. Chin J Pediatr, 2021, 59( 12): 1043- 1047. DOI: 10.3760/cma.j.cn112140-20211004-00843.
王伟, 王薇, 邹丽萍, 等. Ⅰ型干扰素病25例临床特点分析[J]. 中华儿科杂志, 2021, 59( 12): 1043- 1047. DOI: 10.3760/cma.j.cn112140-20211004-00843.
|
| [39] |
GAVAZZI F, CROSS ZM, WOIDILL S, et al. Hepatic involvement in aicardi-goutières syndrome[J]. Neuropediatrics, 2021, 52( 6): 441- 447. DOI: 10.1055/s-0040-1722673.
|
| [40] |
ELHANI I, RILLER Q, BOURSIER G, et al. A20 haploinsufficiency: A systematic review of 177 cases[J]. J Investig Dermatol, 2024, 144( 6): 1282- 1294. DOI: 10.1016/j.jid.2023.12.007.
|
| [41] |
IWASA T, MIWA TK, UNOME S, et al. A case of A20 haploinsufficiency complicated by autoimmune hepatitis[J]. Hepatol Res, 2024, 54( 6): 606- 611. DOI: 10.1111/hepr.14003.
|
| [42] |
KIM HY, SONG JY, KIM WI, et al. The first case of an infant with familial A20 haploinsufficiency in Korea[J]. J Korean Med Sci, 2020, 35( 30): e252. DOI: 10.3346/jkms.2020.35.e252.
|
| [43] |
LI GM, LIU HM, GUAN WZ, et al. Expanding the spectrum of A20 haploinsufficiency in two Chinese families: Cases report[J]. BMC Med Genet, 2019, 20( 1): 124. DOI: 10.1186/s12881-019-0856-1.
|
| [44] |
DESHAYES S, BAZILLE C, KHOURI E EL, et al. Chronic hepatic involvement in the clinical spectrum of A20 haploinsufficiency[J]. Liver Int, 2021, 41( 8): 1894- 1900. DOI: 10.1111/liv.14935.
|
| [45] |
JINDAL AK, PILANIA RK, SURI D, et al. A young female with early onset arthritis, uveitis, hepatic, and renal granulomas: A clinical tryst with Blau syndrome over 20 years and case-based review[J]. Rheumatol Int, 2021, 41( 1): 173- 181. DOI: 10.1007/s00296-019-04316-6.
|
| [46] |
CROPLEY A, ASHRAFY AH, WELTMAN M. An original description of granulomatous liver cirrhosis in Blau syndrome[J]. Dig Dis Sci, 2019, 64( 11): 3346- 3349. DOI: 10.1007/s10620-019-05682-8.
|