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本文引用的文献

1
Histopathologic Correlates of Familial Hemophagocytic Lymphohistiocytosis Isolated to the Central Nervous System.中枢神经系统孤立性家族性噬血细胞性淋巴组织细胞增生症的组织病理学相关性。
J Neuropathol Exp Neurol. 2018 Dec 1;77(12):1079-1084. doi: 10.1093/jnen/nly094.
2
Adult-onset hemophagocytic lymphohistiocytosis type 2 presenting as a demyelinating disease.成人起病的噬血细胞性淋巴组织细胞增生症 2 型表现为脱髓鞘疾病。
Mult Scler Relat Disord. 2018 Oct;25:77-82. doi: 10.1016/j.msard.2018.07.031. Epub 2018 Jul 19.
3
Allogeneic hematopoietic stem cell transplantation is associated with cure and durable remission of late-onset primary isolated central nervous system hemophagocytic lymphohistiocytosis.异基因造血干细胞移植与迟发性原发性孤立性中枢神经系统噬血细胞性淋巴组织细胞增生症的治愈和持久缓解相关。
Pediatr Transplant. 2018 Feb;22(1). doi: 10.1111/petr.13101. Epub 2017 Dec 13.
4
Confirmed efficacy of etoposide and dexamethasone in HLH treatment: long-term results of the cooperative HLH-2004 study.依托泊苷和地塞米松治疗噬血细胞性淋巴组织细胞增生症的确证疗效:HLH - 2004合作研究的长期结果
Blood. 2017 Dec 21;130(25):2728-2738. doi: 10.1182/blood-2017-06-788349. Epub 2017 Sep 21.
5
Perforin and CD107a testing is superior to NK cell function testing for screening patients for genetic HLH.对于筛查遗传性噬血细胞性淋巴组织细胞增生症(HLH)患者,穿孔素和CD107a检测优于自然杀伤(NK)细胞功能检测。
Blood. 2017 Jun 1;129(22):2993-2999. doi: 10.1182/blood-2016-12-753830. Epub 2017 Mar 7.
6
Incidence and Outcomes of Central Nervous System Hemophagocytic Lymphohistiocytosis Relapse after Reduced-Intensity Conditioning Hematopoietic Stem Cell Transplantation.减低强度预处理造血干细胞移植后中枢神经系统噬血细胞性淋巴组织细胞增生症复发的发生率及转归
Biol Blood Marrow Transplant. 2017 May;23(5):857-860. doi: 10.1016/j.bbmt.2017.02.011. Epub 2017 Feb 17.
7
How to Treat Involvement of the Central Nervous System in Hemophagocytic Lymphohistiocytosis?如何治疗噬血细胞性淋巴组织细胞增生症的中枢神经系统受累?
Curr Treat Options Neurol. 2017 Jan;19(1):3. doi: 10.1007/s11940-017-0439-4.
8
Successful treatment of recurrent CNS disease post-bone marrow transplant in children with familial hemophagocytic lymphohistiocytosis.家族性噬血细胞性淋巴组织细胞增生症患儿骨髓移植后复发性中枢神经系统疾病的成功治疗。
Pediatr Blood Cancer. 2016 Dec;63(12):2154-2158. doi: 10.1002/pbc.26175. Epub 2016 Aug 27.
9
The minimum required level of donor chimerism in hereditary hemophagocytic lymphohistiocytosis.遗传性噬血细胞性淋巴组织细胞增生症中供体嵌合的最低要求水平。
Blood. 2016 Jun 23;127(25):3281-90. doi: 10.1182/blood-2015-12-684498. Epub 2016 Apr 20.
10
Familial Hemophagocytic Lymphohistiocytosis.家族性噬血细胞性淋巴组织细胞增生症
Hematol Oncol Clin North Am. 2015 Oct;29(5):903-13. doi: 10.1016/j.hoc.2015.06.008. Epub 2015 Aug 25.

中枢神经系统受限型家族性噬血细胞性淋巴组织细胞增生症对造血细胞移植有反应。

Central nervous system-restricted familial hemophagocytic lymphohistiocytosis responds to hematopoietic cell transplantation.

机构信息

Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA.

Department of Neurology.

出版信息

Blood Adv. 2019 Feb 26;3(4):503-507. doi: 10.1182/bloodadvances.2018027417.

DOI:10.1182/bloodadvances.2018027417
PMID:30760465
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6391665/
Abstract

Familial HLH can present as chronic isolated neuroinflammation. CNS-isolated HLH responds to hematopoietic cell transplantation.

摘要

家族性 HLH 可表现为慢性孤立性神经炎症。中枢神经系统孤立性 HLH 对造血细胞移植有反应。