一个家族中白细胞介素-2诱导型T细胞激酶缺乏症的病程：一名同胞患淋巴瘤样肉芽肿病、淋巴瘤并接受异基因骨髓移植；另一名死亡。 - Suppr

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超能文献

Course of IL-2-inducible T-cell kinase deficiency in a family: lymphomatoid granulomatosis, lymphoma and allogeneic bone marrow transplantation in one sibling; and death in the other.

作者信息

Çağdaş D, Erman B, Hanoğlu D, Tavil B, Kuşkonmaz B, Aydın B, Akyüz C, Uçkan D, Sanal Ö, Tezcan I

机构信息

Hacettepe University İhsan Doğramacı Children's Hospital, Section of Pediatric Immunology, Ankara, Turkey.

Hacettepe University İhsan Doğramacı Children's Hospital, Section of Pediatrics, Ankara, Turkey.

出版信息

Bone Marrow Transplant. 2017 Jan;52(1):126-129. doi: 10.1038/bmt.2016.185. Epub 2016 Jul 25.

DOI:10.1038/bmt.2016.185

PMID:27454071

Abstract

摘要

相似文献

Course of IL-2-inducible T-cell kinase deficiency in a family: lymphomatoid granulomatosis, lymphoma and allogeneic bone marrow transplantation in one sibling; and death in the other.一个家族中白细胞介素-2诱导型T细胞激酶缺乏症的病程：一名同胞患淋巴瘤样肉芽肿病、淋巴瘤并接受异基因骨髓移植；另一名死亡。

Bone Marrow Transplant. 2017 Jan;52(1):126-129. doi: 10.1038/bmt.2016.185. Epub 2016 Jul 25.

[Primary and isolated cutaneous lymphomatoid granulomatosis following heart-lung transplantation].[心肺移植术后原发性孤立性皮肤淋巴瘤样肉芽肿病]

Ann Dermatol Venereol. 2000 May;127(5):488-91.

Treatment of patients with myelodysplastic syndromes with allogeneic bone marrow transplantation from genotypically HLA-identical sibling and alternative donors.采用来自基因型 HLA 相同的同胞及替代供者的异基因骨髓移植治疗骨髓增生异常综合征患者。

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Allogeneic bone marrow transplantation for relapsed and refractory lymphoma using genotypically HLA-identical and alternative donors.使用基因分型 HLA 相同和替代供体进行异基因骨髓移植治疗复发难治性淋巴瘤。

J Clin Oncol. 1991 Oct;9(10):1848-59. doi: 10.1200/JCO.1991.9.10.1848.

Lymphomatoid granulomatosis following autologous stem cell transplantation.自体干细胞移植后发生的淋巴瘤样肉芽肿病。

Bone Marrow Transplant. 1999 Jan;23(1):79-81. doi: 10.1038/sj.bmt.1701513.

[A study of T-cell reconstitution after HLA-matched sibling bone marrow transplantation in leukemia patients].[白血病患者中人类白细胞抗原匹配同胞骨髓移植后T细胞重建的研究]

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The effects of bereavement on adult sibling bone marrow donors' psychological well-being and reactions to donation.丧亲之痛对成年同胞骨髓捐赠者心理健康及捐赠反应的影响。

Bone Marrow Transplant. 1998 Jan;21(2):181-8. doi: 10.1038/sj.bmt.1701063.

Allogeneic bone marrow transplantation for poor-prognosis lymphoma: response, toxicity and survival depend on disease histology.异基因骨髓移植治疗预后不良淋巴瘤：反应、毒性和生存情况取决于疾病组织学类型。

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No disadvantage in outcome of using matched unrelated donors as compared with matched sibling donors for bone marrow transplantation in children with acute lymphoblastic leukemia in second remission.对于处于第二次缓解期的急性淋巴细胞白血病儿童，与匹配的同胞供者相比，使用匹配的无关供者进行骨髓移植在治疗结果上并无劣势。

J Clin Oncol. 2001 Jul 15;19(14):3406-14. doi: 10.1200/JCO.2001.19.14.3406.

Comparison of the outcomes of allogeneic bone marrow transplantation from partially mismatched related donors, matched sibling donors, and matched unrelated donors in Japanese pediatric patients: a single center result.日本儿科患者中来自部分不匹配相关供者、匹配同胞供者及匹配无关供者的异基因骨髓移植结局比较：单中心结果

Pediatr Transplant. 2004 Jun;8(3):260-6. doi: 10.1111/j.1399-3046.2004.00161.x.

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本文引用的文献

Interleukin-2-inducible T-cell kinase (ITK) deficiency - clinical and molecular aspects.白细胞介素-2诱导型T细胞激酶（ITK）缺乏症——临床和分子学方面

J Clin Immunol. 2014 Nov;34(8):892-9. doi: 10.1007/s10875-014-0110-8. Epub 2014 Oct 24.

Hematopoietic stem cell transplantation conditioning with use of rituximab in EBV related lymphoproliferative disorders.利妥昔单抗在 EBV 相关淋巴组织增生性疾病造血干细胞移植预处理中的应用。

Clin Immunol. 2014 Apr;151(2):79-83. doi: 10.1016/j.clim.2014.01.007. Epub 2014 Feb 4.

Innate immune control of EBV-infected B cells by invariant natural killer T cells.固有免疫通过不变自然杀伤 T 细胞控制 EBV 感染的 B 细胞。

Blood. 2013 Oct 10;122(15):2600-8. doi: 10.1182/blood-2013-01-480665. Epub 2013 Aug 23.

IL-2-inducible T-cell kinase deficiency with pulmonary manifestations due to disseminated Epstein-Barr virus infection.由弥散性 Epstein-Barr 病毒感染引起的伴有肺部表现的白细胞介素 2 诱导型 T 细胞激酶缺乏症。

Int Arch Allergy Immunol. 2012;158(4):418-22. doi: 10.1159/000333472. Epub 2012 Apr 5.

Loss-of-function mutations within the IL-2 inducible kinase ITK in patients with EBV-associated lymphoproliferative diseases.IL-2 诱导激酶 ITK 失活突变与 EBV 相关淋巴组织增生性疾病。

Leukemia. 2012 May;26(5):963-71. doi: 10.1038/leu.2011.371. Epub 2012 Jan 6.

IL-2-inducible T-cell kinase deficiency: clinical presentation and therapeutic approach.白细胞介素-2 诱导的 T 细胞激酶缺乏症：临床表现与治疗方法。

Haematologica. 2011 Mar;96(3):472-6. doi: 10.3324/haematol.2010.033910. Epub 2010 Nov 25.

Effective and long-term control of EBV PTLD after transfer of peptide-selected T cells.肽段选择的 T 细胞移植后对 EBV-PTLD 的有效和长期控制。

Blood. 2010 Apr 8;115(14):2960-70. doi: 10.1182/blood-2009-08-236356. Epub 2010 Jan 26.

Girls homozygous for an IL-2-inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation.因白细胞介素-2诱导型T细胞激酶突变而纯合的女孩，该突变导致蛋白质缺乏，她们会发展出致命的与EB病毒相关的淋巴细胞增殖。

J Clin Invest. 2009 May;119(5):1350-8. doi: 10.1172/jci37901.

Pulmonary parenchymal involvement of low-grade lymphoproliferative disorders.低度淋巴增殖性疾病的肺实质受累

J Comput Assist Tomogr. 2005 Nov-Dec;29(6):825-30. doi: 10.1097/01.rct.0000179597.93844.23.

Lymphocyte subsets in healthy children from birth through 18 years of age: the Pediatric AIDS Clinical Trials Group P1009 study.从出生到18岁健康儿童的淋巴细胞亚群：儿科艾滋病临床试验组P1009研究

J Allergy Clin Immunol. 2003 Nov;112(5):973-80. doi: 10.1016/j.jaci.2003.07.003.

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