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低剂量HA方案治疗难治性、复发性AA-PNH综合症1例并文献复习 被引量:3

A case of refractory and recurrent AA-PNH syndrome treated with low-dose HA regimen and literature review
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摘要 再生障碍性贫血(AA)及阵发性睡眠性血红蛋白尿(PNH)均是常见疾病,二者经常演变为AAPNH综合症。对于难治性、复发性AA-PNH患者,常规治疗效果甚差。我院采用低剂量HA方案治疗1例年轻女性患者,取得了比较满意的效果,现报告如下,并综合相关文献进行分析讨论。1病例资料患者,女,22岁,因头晕、乏力8个月余,于2010年9月14日入院。体检:重度贫血貌,全身皮肤黏膜苍白,巩膜无黄染,浅表淋巴结未肿大。 AA and PNH are common diseases,both of which often evolve into AA-PNH syndrome.For patients with refractory and recurrent AA-PNH syndrome,the curative effect of conventional therapy is very poor.We treated a young female patient with low-dose HA regimen and achieved satisfactory results,now it is reported as follows and related literature are discussed.
机构地区 核工业
出处 《临床血液学杂志》 CAS 2015年第6期996-998,共3页 Journal of Clinical Hematology
关键词 再生障碍性贫血-阵发性睡眠性血红蛋白尿综合症 难治性 复发性 低剂量 联合化疗 aplastic anemia-paroxysmal nocturnal hemoglobinuria syndrom refrctory relapsed low dose com-bined chemotherapy
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  • 1Richards SJ, Hill A, Hillmen P. Recent advances in the diagnosis, monitoring, and management of patients with paroxysmal nocturnal hemoglobinuria. Cytometry B Clin Cytom, 2007, 72(5) :291-298.
  • 2Saso R, Marsh J, Cevreska L, et al. Bone marrow transplantation for paroxysmal nocturnal hemoglobinuria. Haematologica, 1999, 104(2):392-396.
  • 3Lee JL, Lee JH, Lee JH, et al. Allogeneic hematopoietic cell transplantation for paroxysmal nocturnal hemoglobinuria. Eur J haematol, 2003, 71 (2) : 114-118.
  • 4张之南,血液病诊断及疗效标准(第2版),1998年,88页
  • 5邵宗鸿,中华血液学杂志,1997年,18卷,10期,544页
  • 6Karadimitris A, Luzzatto L. The cellular pathogenesis of paroxysmal nocturnal hemoglobinuria. Leukemia,2001,15:1148-1152.
  • 7Alfinito F,lo Pardo C, Boccuni P, et al. Reliable identification of the PNH defect on lymphocyte and monocyte membrane by CD48 MoAbs, In:Kishimoto T, Kikutani I I, von dem Borne AEG, et al. eds. Leukocyte Typing Ⅵ. New York: Garland Publishing, 1997. 512
  • 8Rosti V, Tremml G, Soares V, et al. Embryonic stem cells without pig-a gene activity are competent for hematopoiesis with the PNH phenotype but not for clonal expansion.J Clin Invest,1997,100:1028-1036.
  • 9Taylor VC,Sims M, Brett S, et al. Antibody selection against CD52 produces a paroxysmal nocturnal haemoglobinuria phenotype in human lymphocytes by a novel mechanism. Biochem J,1997,322:919-925.
  • 10Boccuni P,del Vecchio L,di Noto R,et al. Glycosyl-phosphatidylinositol (GPI)-anchored molecues and the pathogenesis of paroxysmal nocturnal hemoglobinuria. Crit Rev Oncol Hematol, 2000,33:25-43.

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