以多发静脉血栓为首发表现的骨髓增生异常综合征伴白塞病一例_West China Medical Journal

Authors：

代明辉 ^1,2 , 帅晓 ¹ ,  吴俣 ¹

1. ;
2. ;

Corresponding author：

吴俣, Email: wu_yu@scu.edu.cn

Keywords：

骨髓增生异常综合征; 白塞病; +8 染色体; 血栓; 溃疡

DOI：

10.7507/1002-0179.202202027

Video：

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Citation： 代明辉, 帅晓, 吴俣. 以多发静脉血栓为首发表现的骨髓增生异常综合征伴白塞病一例. West China Medical Journal, 2023, 38(1): 147-150. doi: 10.7507/1002-0179.202202027 Copy

1.	中华医学会血液学分会. 骨髓增生异常综合征中国诊断与治疗指南(2019 年版). 中华血液学杂志, 2019, 40(2): 89-97.
2.	Lee S. Diagnostic criteria of Behçet’s disease: problems and suggestions. Yonsei Med J, 1997, 38(6): 365-369.
3.	Greenberg PL, Tuechler H, Schanz J, et al. Revised international prognostic scoring system for myelodysplastic syndromes. Blood, 2012, 120(12): 2454-2465.
4.	Kristinsson SY, Björkholm M, Hultcrantz M, et al. Chronic immune stimulation might act as a trigger for the development of acute myeloid leukemia or myelodysplastic syndromes. J Clin Oncol, 2011, 29(21): 2897-2903.
5.	Utley SM. Myelodysplastic syndromes. Semin Oncol Nurs, 1996, 12(1): 51-58.
6.	Ozguler Y, Hatemi G. Management of Behçet’s syndrome. Curr Opin Rheumatol, 2016, 28(1): 45-50.
7.	Haga N, Iwata H, Yamaguchi Y, et al. Mucocutaneous pyoderma gangrenosum due to trisomy 8 neutrophilic infiltrates in a patient with myelodysplastic syndrome. Br J Dermatol, 2016, 174(1): 239-241.
8.	Komrokji RS, Kulasekararaj A, Al Ali NH, et al. Autoimmune diseases and myelodysplastic syndromes. Am J Hematol, 2016, 91(5): E280-E283.
9.	Seguier J, Gelsi-Boyer V, Ebbo M, et al. Autoimmune diseases in myelodysplastic syndrome favors patients survival: a case control study and literature review. Autoimmun Rev, 2019, 18(1): 36-42.
10.	Ivy KS, Brent Ferrell P. Disordered immune regulation and its therapeutic targeting in myelodysplastic syndromes. Curr Hematol Malig Rep, 2018, 13(4): 244-255.
11.	Kimura S, Kuroda J, Akaogi T, et al. Trisomy 8 involved in myelodysplastic syndromes as a risk factor for intestinal ulcers and thrombosis: Behçet’s syndrome. Leuk Lymphoma, 2001, 42(1/2): 115-121.
12.	Chen G, Zeng W, Miyazato A, et al. Distinctive gene expression profiles of CD34 cells from patients with myelodysplastic syndrome characterized by specific chromosomal abnormalities. Blood, 2004, 104(13): 4210-4218.
13.	Cagnin S, Biscuola M, Patuzzo C, et al. Reconstruction and functional analysis of altered molecular pathways in human atherosclerotic arteries. BMC Genomics, 2009, 10: 13.
14.	Grainger DJ. Transforming growth factor beta and atherosclerosis: so far, so good for the protective cytokine hypothesis. Arterioscler Thromb Vasc Biol, 2004, 24(3): 399-404.
15.	欧阳, 吴俣. 骨髓增生异常综合征免疫异常机制的研究新进展. 国际输血及血液学杂志, 2021, 44(1): 22-28.
16.	Yazici H, Seyahi E, Hatemi G, et al. Behçet syndrome: a contemporary view. Nat Rev Rheumatol, 2018, 14(2): 119.
17.	Hatemi G, Seyahi E, Fresko I, et al. One year in review 2020: Behçet’s syndrome. Clin Exp Rheumatol, 2020, 38(5, Suppl 127): 3-10.
18.	Shen Y, Ma HF, Luo D, et al. High incidence of gastrointestinal ulceration and cytogenetic aberration of trisomy 8 as typical features of Behçet’s disease associated with myelodysplastic syndrome: a series of 16 consecutive Chinese patients from the Shanghai Behçet’s disease database and comparison with the literature. Biomed Res Int, 2018, 2018: 8535091.
19.	Handa T, Nakatsue T, Baba M, et al. Clinical features of three cases with pulmonary alveolar proteinosis secondary to myelodysplastic syndrome developed during the course of Behçet’s disease. Respir Investig, 2014, 52(1): 75-79.
20.	Ahn JK, Cha HS, Koh EM, et al. Behcet’s disease associated with bone marrow failure in Korean patients: clinical characteristics and the association of intestinal ulceration and trisomy 8. Rheumatology (Oxford), 2008, 47(8): 1228-1230.
21.	Toyonaga T, Nakase H, Matsuura M, et al. Refractoriness of intestinal Behçet’s disease with myelodysplastic syndrome involving trisomy 8 to medical therapies - our case experience and review of the literature. Digestion, 2013, 88(4): 217-221.
22.	Kawano S, Hiraoka S, Okada H, et al. Clinical features of intestinal Behçet’s disease associated with myelodysplastic syndrome and trisomy 8. Acta Med Okayama, 2015, 69(6): 365-369.
23.	Hulscher JB, van den Berg HP, Siegert CE, et al. A Turkish man with Behçet disease and recurrent acute abdomen. Ned Tijdschr Geneeskd, 2003, 147(40): 1969-1971.
24.	Tanaka H, Shimizu N, Tougasaki E, et al. Successful treatment by azacitidine therapy of intestinal Behçet’s disease associated with myelodysplastic syndrome. Int J Hematol, 2013, 97(4): 520-524.
25.	Yilmaz U, Ar MC, Esatoglu SN, et al. How to treat myelodysplastic syndrome with clinical features resembling Behçet syndrome: a case-based systematic review. Ann Hematol, 2020, 99(6): 1193-1203.
26.	Fenaux P, Platzbecker U, Mufti GJ, et al. Luspatercept in patients with lower-risk myelodysplastic syndromes. N Engl J Med, 2020, 382(2): 140-151.

1. 中华医学会血液学分会. 骨髓增生异常综合征中国诊断与治疗指南(2019 年版). 中华血液学杂志, 2019, 40(2): 89-97.
2. Lee S. Diagnostic criteria of Behçet’s disease: problems and suggestions. Yonsei Med J, 1997, 38(6): 365-369.
3. Greenberg PL, Tuechler H, Schanz J, et al. Revised international prognostic scoring system for myelodysplastic syndromes. Blood, 2012, 120(12): 2454-2465.
4. Kristinsson SY, Björkholm M, Hultcrantz M, et al. Chronic immune stimulation might act as a trigger for the development of acute myeloid leukemia or myelodysplastic syndromes. J Clin Oncol, 2011, 29(21): 2897-2903.
5. Utley SM. Myelodysplastic syndromes. Semin Oncol Nurs, 1996, 12(1): 51-58.
6. Ozguler Y, Hatemi G. Management of Behçet’s syndrome. Curr Opin Rheumatol, 2016, 28(1): 45-50.
7. Haga N, Iwata H, Yamaguchi Y, et al. Mucocutaneous pyoderma gangrenosum due to trisomy 8 neutrophilic infiltrates in a patient with myelodysplastic syndrome. Br J Dermatol, 2016, 174(1): 239-241.
8. Komrokji RS, Kulasekararaj A, Al Ali NH, et al. Autoimmune diseases and myelodysplastic syndromes. Am J Hematol, 2016, 91(5): E280-E283.
9. Seguier J, Gelsi-Boyer V, Ebbo M, et al. Autoimmune diseases in myelodysplastic syndrome favors patients survival: a case control study and literature review. Autoimmun Rev, 2019, 18(1): 36-42.
10. Ivy KS, Brent Ferrell P. Disordered immune regulation and its therapeutic targeting in myelodysplastic syndromes. Curr Hematol Malig Rep, 2018, 13(4): 244-255.
11. Kimura S, Kuroda J, Akaogi T, et al. Trisomy 8 involved in myelodysplastic syndromes as a risk factor for intestinal ulcers and thrombosis: Behçet’s syndrome. Leuk Lymphoma, 2001, 42(1/2): 115-121.
12. Chen G, Zeng W, Miyazato A, et al. Distinctive gene expression profiles of CD34 cells from patients with myelodysplastic syndrome characterized by specific chromosomal abnormalities. Blood, 2004, 104(13): 4210-4218.
13. Cagnin S, Biscuola M, Patuzzo C, et al. Reconstruction and functional analysis of altered molecular pathways in human atherosclerotic arteries. BMC Genomics, 2009, 10: 13.
14. Grainger DJ. Transforming growth factor beta and atherosclerosis: so far, so good for the protective cytokine hypothesis. Arterioscler Thromb Vasc Biol, 2004, 24(3): 399-404.
15. 欧阳, 吴俣. 骨髓增生异常综合征免疫异常机制的研究新进展. 国际输血及血液学杂志, 2021, 44(1): 22-28.
16. Yazici H, Seyahi E, Hatemi G, et al. Behçet syndrome: a contemporary view. Nat Rev Rheumatol, 2018, 14(2): 119.
17. Hatemi G, Seyahi E, Fresko I, et al. One year in review 2020: Behçet’s syndrome. Clin Exp Rheumatol, 2020, 38(5, Suppl 127): 3-10.
18. Shen Y, Ma HF, Luo D, et al. High incidence of gastrointestinal ulceration and cytogenetic aberration of trisomy 8 as typical features of Behçet’s disease associated with myelodysplastic syndrome: a series of 16 consecutive Chinese patients from the Shanghai Behçet’s disease database and comparison with the literature. Biomed Res Int, 2018, 2018: 8535091.
19. Handa T, Nakatsue T, Baba M, et al. Clinical features of three cases with pulmonary alveolar proteinosis secondary to myelodysplastic syndrome developed during the course of Behçet’s disease. Respir Investig, 2014, 52(1): 75-79.
20. Ahn JK, Cha HS, Koh EM, et al. Behcet’s disease associated with bone marrow failure in Korean patients: clinical characteristics and the association of intestinal ulceration and trisomy 8. Rheumatology (Oxford), 2008, 47(8): 1228-1230.
21. Toyonaga T, Nakase H, Matsuura M, et al. Refractoriness of intestinal Behçet’s disease with myelodysplastic syndrome involving trisomy 8 to medical therapies - our case experience and review of the literature. Digestion, 2013, 88(4): 217-221.
22. Kawano S, Hiraoka S, Okada H, et al. Clinical features of intestinal Behçet’s disease associated with myelodysplastic syndrome and trisomy 8. Acta Med Okayama, 2015, 69(6): 365-369.
23. Hulscher JB, van den Berg HP, Siegert CE, et al. A Turkish man with Behçet disease and recurrent acute abdomen. Ned Tijdschr Geneeskd, 2003, 147(40): 1969-1971.
24. Tanaka H, Shimizu N, Tougasaki E, et al. Successful treatment by azacitidine therapy of intestinal Behçet’s disease associated with myelodysplastic syndrome. Int J Hematol, 2013, 97(4): 520-524.
25. Yilmaz U, Ar MC, Esatoglu SN, et al. How to treat myelodysplastic syndrome with clinical features resembling Behçet syndrome: a case-based systematic review. Ann Hematol, 2020, 99(6): 1193-1203.
26. Fenaux P, Platzbecker U, Mufti GJ, et al. Luspatercept in patients with lower-risk myelodysplastic syndromes. N Engl J Med, 2020, 382(2): 140-151.

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以多发静脉血栓为首发表现的骨髓增生异常综合征伴白塞病一例

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