Abstract:Objective To study the clinical and laboratory characteristics of chronic active Epstein-Barr virus(EBV) infection (CAEBV) in children and to provide a basis for the diagnosis and treatment of CAEBV. Methods The clinical data of 13 children with CAEBV, as well as 15 cases of acute EBV infection (AEBV) as controls, wereanalyzed, including clinical manifestations, EBV antibodies, EBV DNA, and peripheral blood lymphocyte subsets.Results Both groups of patients had infectious mononucleosis-like symptoms such as fever, hepatomegaly,splenomegaly, and lymphadenectasis, but CAEBV patients had a longer course of disease and continuous and recurrentsymptoms. Compared with the AEBV group, the CAEBV group had a significantly higher EBV DNA load in peripheralblood (P<0.05), a significantly higher VCA-IgG titer (P<0.05), and significantly lower numbers of white blood cells,lymphocytes, B cells, total T cells, CD4+ T cells, and CD8+ T cells in peripheral blood (P<0.05). Among 13 CAEBVpatients followed up, 8 cases died, 2 cases showed an improvement, 2 cases had a recurrence, and 1 case was lost tofollow-up after being transferred to another hospital. All the AEBV patients were cured and had no recurrence during theone-year follow-up. Conclusions The clinical manifestations of CAEBV vary in children. It is difficult to distinguish CAEBV from AEBV early. More attention should be paid to CAEBV because of its severe complications, poorprognosis, and high mortality. Measurement of EBV DNA load, VCA-IgG titer, and lymphocyte subsets in peripheralblood may be helpful in the diagnosis and differential diagnosis of CAEBV.
MAO Jun-Qing,YANG Shi-Long,SONG Hua et al. Clinical and laboratory characteristics of chronic active Epstein-Barr virus infectionin children[J]. CJCP, 2014, 16(11): 1081-1085.
Okano M, Kawa K, Kimura H, et al. Proposed guidelines for diagnosing chronic active Epstein-Barr virus infection[J]. Am J Hematol, 2005, 80(1):64-69.
[5]
Wakiguchi H, Maeda A, Dohno S, et al. Infectious mononucleosis[J]. Nihon Rinsho, 2006, 64(3):625-629.
[6]
Kimura H, Hoshino Y, Kanegane H, et al. Clinical and virologic characteristics of chronic active Epstein-Barr virus infection[J]. Blood, 2001, 98(2):280-286.
[7]
Lu G, Xie ZD, Zhao SY, et al. Clincical analysis and followup study of chronic active Epstein-Barr virus infection in 53 pediatric cases[J]. Chin Med J, 2009, 122(3):262-266.
[8]
Hong M, Ko YH, Yoo KH, et al. EBV-positive T/NK-cell lymphoproliferative disease of childhood[J]. Korean J Pathol, 2003, 47(2):137-147.
Yamashita N, Kimura H, Morishima T. Virological aspects of Epstein-Barr virus infections [J]. Acta Med Okayama, 2005, 59(6):239-246.
[12]
Bollard CM, Gottschalk S, Leen AM, et al. Complete responses of relapsed lymphoma following genetic modification of tumorantigen presenting cells and T-lymphocyte transfer [J]. Blood, 2007, 110(8):2838-2845.
Grywalska E, Markowicz J, Crabarczyk P, et al. Epstein-Barr virus-associated lymphoproliferative disorders[J]. Postepy Hig Med Dosw (online), 2013, 67(5):481-490.
[15]
Carbone A, Gloghinia A, Dotti G. EBV-associated lymphoproliferative disorders:classification and treatment[J]. Oncologist, 2008, 13(5):577-585.
[16]
Cohen JI, Jaffe ES, Dale JK, et al. Characterization and treatment of chronic active Epstein-Barr virus disease:a 28-year experience in the United States[J]. Blood, 2011, 117(22):5835-5849.