期刊文献+

伴EB病毒感染的淋巴瘤继发噬血细胞综合征四例 被引量:1

原文传递
导出
摘要 目的探讨伴EB病毒(EBV)感染的淋巴瘤继发噬血细胞综合征(HPS)的临床特征。方法分析4例伴EB病毒感染的淋巴瘤继发HPS患者的临床资料,并文献复习。结果3例患者初诊为EBV继发HPS,4例患者最终均诊断为T细胞淋巴瘤。临床共同特点为发热、脾大、全血细胞减少、铁蛋白升高和低纤维蛋白原血症,浅表淋巴结肿大不明显,3例患者存在肝功能异常。4例患者抗EBV治疗后EBV—DNA均无明显下降。4例患者采用甲泼尼龙联合环孢素、依托?自苷或氟达拉滨治疗HPS,其中1例患者在激素减量过程中复发,规范化疗后HPS得以控制。结论伴EBV感染的淋巴瘤继发HIPS易被误诊为单纯EBV感染继发HPS。临床抗病毒效果欠佳或治疗过程中出现HPS反复需要警惕潜在淋巴瘤可能,需要多次取材送病理检查,甚至进行PET-CT检查积极寻找原发病,此类疾病的治疗原则是在积极治疗控制HPS后立即开始针对淋巴瘤的规范化疗。
出处 《白血病.淋巴瘤》 CAS 2011年第8期494-496,共3页 Journal of Leukemia & Lymphoma
基金 首都医学发展科研基金(2009-1032)
  • 相关文献

参考文献9

  • 1Janka G,Imashulku S,Elinder G,et al.Infection and malignancy-associated hemophagocytic syndromes.Secondary hemophagocytic lymphohistiocytosis.Hematol Oncol Clin North Am,1998,12:435.
  • 2Han AR,Lee HR,Park BB,et al.Lymphoma-associated hemophagocytic syndrome:clinical features and treatment outcome.Ann Hematol,2007,86:493-498.
  • 3Gao J,Luo X,Tang K,et al.Epstein-Barr virus integrates frequently into chromosome 4q,2q,1q and 7q of Burkitt's lymphoma cell line (Raji).J Virol Methods,2006,136:193-199.
  • 4Liu MT,Chang YT,Chen SC,et al.Epstein-Barr virus latent membrane protein 1 represses p53-mediated DNA repair and transcriptional activity.Oncogene,2005,24:2635-2646.
  • 5Dawson CW,Tramountanis G,Eliopoulos AG,et al.Epstein-Barr virus latent membrane protein I (LMPI) activates the phosphatidylinositol 3-kinase/Akt pathway to promote cell survival and induce actin filament remodeling.J Biol Chem,2003,278:3694-3704.
  • 6Henter JI.HLH-2004:Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis.Pediatr Blood Cancer,2007,48:124-131.
  • 7Filipovich AH.Hemophagocytic lymphohistiocytosis (HLH) and related disorders.Hematology,2009,1:127-131.
  • 8Kontopoulou T,Tsaousis G,Vaidakis E,et al.Hemophagocytic syndrome in association with visceral leishmaniasis.Am J Med,2002,113:439-440.
  • 9王旖旎,王昭,吴林,岑溪南,李渤涛,宁丰,段学章,李娟.多中心72例噬血细胞综合征诊疗分析[J].中华血液学杂志,2009,30(12):793-798. 被引量:98

二级参考文献9

共引文献97

同被引文献18

  • 1Introne W,Boissy RE,Gahl WA. Clinical,molecular,and cell biological aspects of Chediak-Higashi syndrome[J].Molecular Genetics and Metabolism,1999,(02):283-303.
  • 2Shiflett SL,Kaplan J,Ward DM. Chediak-Higashi syndrome:a rare disorder of lysosomes and lysosome related organelles[J].Pigment Cell Research,2002,(04):251-257.
  • 3Ward DM,Griffiths GM,Stinchcombe JC. Analysis of the lysosomal storage disease Chediak-Higashi syndrome[J].TRAFFIC,2000,(11):816-822.
  • 4Kaplan J,De Domenico I,Ward DM. Chediak-Higashi syndrome[J].Current Opinions in Hematology,2008,(01):22-29.
  • 5Fantinato GT,Cestari Sda C,Afonso JP. Do you know this syndrome? Chediak-Higashi syndrome[J].Anais Brasileiros de Dermatologia,2011,(05):1029.
  • 6Pullarkat ST. Accelerated phase of Chediak-Higashi syndrome[J].Blood,2012,(01):5.
  • 7Reddy RR,Babu BM,Venkateshwaramma B. Silvery hair syndrome in two cousins:Chediak-Higashi syndrome vs Griscelli syndrome,with rare associations[J].Int J Trichology,2011,(02):107-111.
  • 8Roy A,Kar R,Basu D. Clinico-hematological profile of Chediak-Higashi syndrome:experience from a tertiary care center in south India[J].Indian Journal of Pathology and Microbiology,2011,(03):547-551.
  • 9Abdulsalam AH,Sabeeh N,Bain BJ. Bone marrow aspirate in Chédiak-Higashi syndrome[J].American Journal of Hematology,2012,(01):100.
  • 10Katano H,Ali MA,Patera AC. Chronic active EpsteinBarr virus infection associated with mutations in perforin that impair its maturation[J].Blood,2004,(04):1244-1252.

引证文献1

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部