成人斯蒂爾病并發噬血細胞綜合征一例_West China Medical Journal

Authors：

馬彥鳳 , 薛心雨 ,  徐才剛

四川大學華西醫院血液內科（成都 610041）;

Corresponding?author：

徐才剛, Email: xucaigang@wchscu.cn

Keywords：

成人斯蒂爾病; 噬血細胞綜合征; 早期識別

DOI：

10.7507/1002-0179.202412270

Video：

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Citation： 馬彥鳳, 薛心雨, 徐才剛. 成人斯蒂爾病并發噬血細胞綜合征一例. West China Medical Journal, 2025, 40(4): 675-678. doi: 10.7507/1002-0179.202412270 Copy

1.	劉娟娟, 劉穎, 任菁菁. 常見未分化疾病的全科處理探討. 中國全科醫學, 2015, 18(32): 3985-3987.
2.	Henter JI, Horne A, Aricó M, et al. HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer, 2007, 48(2): 124-131.
3.	Carter SJ, Tattersall RS, Ramanan AV. Macrophage activation syndrome in adults: recent advances in pathophysiology, diagnosis and treatment. Rheumatology (Oxford), 2019, 58(1): 5-17.
4.	Nirmala N, Brachat A, Feist E, et al. Gene-expression analysis of adult-onset Still’s disease and systemic juvenile idiopathic arthritis is consistent with a continuum of a single disease entity. Pediatr Rheumatol Online J, 2015, 13: 50.
5.	吳婷婷, 唐亮, 胡豫. 噬血細胞綜合征的病因和診斷. 臨床血液學雜志, 2024, 37(9): 677-682.
6.	Feist E, Mitrovic S, Fautrel B. Mechanisms, biomarkers and targets for adult-onset Still’s disease. Nat Rev Rheumatol, 2018, 14(10): 603-618.
7.	Gerfaud-Valentin M, Cottin V, Jamilloux Y, et al. Parenchymal lung involvement in adult-onset Still disease: a STROBE-compliant case series and literature review. Medicine (Baltimore), 2016, 95(30): e4258.
8.	Mitrovic S, Fautrel B. Complications of adult-onset Still’s disease and their management. Expert Rev Clin Immunol, 2018, 14(5): 351-365.
9.	Gao Q, Yuan Y, Wang Y, et al. Clinical characteristics of macrophage activation syndrome in adult-onset Still’s disease. Clin Exp Rheumatol, 2021, 39(5 Suppl 132): 59-66.
10.	Yamaguchi M, Ohta A, Tsunematsu T, et al. Preliminary criteria for classification of adult Still’s disease. J Rheumatol, 1992, 19(3): 424-430.
11.	Kumar B, Aleem S, Saleh H, et al. A personalized diagnostic and treatment approach for macrophage activation syndrome and secondary hemophagocytic lymphohistiocytosis in adults. J Clin Immunol, 2017, 37(7): 638-643.
12.	Giacomelli R, Caporali R, Ciccia F, et al. Expert consensus on the treatment of patients with adult-onset still’s disease with the goal of achieving an early and long-term remission. Autoimmun Rev, 2023, 22(12): 103400.
13.	中華醫學會兒科學分會風濕病學組, 中國醫師協會風濕免疫科醫師分會兒科學組, 海峽兩岸醫藥衛生交流協會風濕免疫病學專業委員會兒童學組, 等. 全身型幼年特發性關節炎及合并巨噬細胞活化綜合征診療專家共識(2022 版). 中華實用兒科臨床雜志, 2022, 37(20): 1539-1548.

1. 劉娟娟, 劉穎, 任菁菁. 常見未分化疾病的全科處理探討. 中國全科醫學, 2015, 18(32): 3985-3987.
2. Henter JI, Horne A, Aricó M, et al. HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer, 2007, 48(2): 124-131.
3. Carter SJ, Tattersall RS, Ramanan AV. Macrophage activation syndrome in adults: recent advances in pathophysiology, diagnosis and treatment. Rheumatology (Oxford), 2019, 58(1): 5-17.
4. Nirmala N, Brachat A, Feist E, et al. Gene-expression analysis of adult-onset Still’s disease and systemic juvenile idiopathic arthritis is consistent with a continuum of a single disease entity. Pediatr Rheumatol Online J, 2015, 13: 50.
5. 吳婷婷, 唐亮, 胡豫. 噬血細胞綜合征的病因和診斷. 臨床血液學雜志, 2024, 37(9): 677-682.
6. Feist E, Mitrovic S, Fautrel B. Mechanisms, biomarkers and targets for adult-onset Still’s disease. Nat Rev Rheumatol, 2018, 14(10): 603-618.
7. Gerfaud-Valentin M, Cottin V, Jamilloux Y, et al. Parenchymal lung involvement in adult-onset Still disease: a STROBE-compliant case series and literature review. Medicine (Baltimore), 2016, 95(30): e4258.
8. Mitrovic S, Fautrel B. Complications of adult-onset Still’s disease and their management. Expert Rev Clin Immunol, 2018, 14(5): 351-365.
9. Gao Q, Yuan Y, Wang Y, et al. Clinical characteristics of macrophage activation syndrome in adult-onset Still’s disease. Clin Exp Rheumatol, 2021, 39(5 Suppl 132): 59-66.
10. Yamaguchi M, Ohta A, Tsunematsu T, et al. Preliminary criteria for classification of adult Still’s disease. J Rheumatol, 1992, 19(3): 424-430.
11. Kumar B, Aleem S, Saleh H, et al. A personalized diagnostic and treatment approach for macrophage activation syndrome and secondary hemophagocytic lymphohistiocytosis in adults. J Clin Immunol, 2017, 37(7): 638-643.
12. Giacomelli R, Caporali R, Ciccia F, et al. Expert consensus on the treatment of patients with adult-onset still’s disease with the goal of achieving an early and long-term remission. Autoimmun Rev, 2023, 22(12): 103400.
13. 中華醫學會兒科學分會風濕病學組, 中國醫師協會風濕免疫科醫師分會兒科學組, 海峽兩岸醫藥衛生交流協會風濕免疫病學專業委員會兒童學組, 等. 全身型幼年特發性關節炎及合并巨噬細胞活化綜合征診療專家共識(2022 版). 中華實用兒科臨床雜志, 2022, 37(20): 1539-1548.

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West China Medical Journal

成人斯蒂爾病并發噬血細胞綜合征一例

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