Persistent human parvovirus B19 infection in children under maintenance chemotherapy for acute lymphocytic leukemia

被引:18
|
作者
Fattet, S
Cassinotti, P
Popovic, MB
机构
[1] Univ Hosp, Pediat Oncol & Hematol Unit, CH-1011 Lausanne, Switzerland
[2] Inst Clin Microbiol & Immunol, St Gallen, Switzerland
关键词
acute lymphocytic leukemia; human parvovirus B19; cytopenia; intravenous immunoglobulin; immunodeficiency;
D O I
10.1097/01.mph.0000134463.09543.99
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: To report on B19 infection management and chemotherapy schedule consequences in five children treated for acute lymphocytic leukemia (ALL). Patients and Methods: Between May 2001 and February 2002, five patients between 4 and 12 years of age, receiving maintenance chemotherapy for ALL, presented with symptoms suggesting B 19 infection (pallor, fatigue, petechiae and pancytopenia in four patients; generalized rash in two patients; acute hepatitis in one patient). Qualitative polymerase chain reaction (PCR) on peripheral blood was used for diagnosis and follow-up of infection; quantitative PCR was used for viral load measurement. Intravenous nonspecific high-dose immunoglobulin therapy was administered until PCR was negative. Results: Qualitative B 19 DNA was found in the peripheral blood of all patients, confirming the infection. Viral load at diagnosis ranged from 10(4) to 10(8) particles/mL blood. B 19 DNA was detectable in four patients at 45, 21, 40, and 44 weeks, respectively. Chemotherapy was delayed in all patients. No clear benefit of intravenous immunoglobulin was noted. Conclusions: infection with B 19 is rarely reported in patients with ALL, but it should be suspected when unexplained pancytopenia occurs during chemotherapy. Persistent B19 infection remains a challenge in the management of patients receiving maintenance chemotherapy for ALL, as no specific therapy such as a specific immunoglobulin or vaccine exists. The role of viral load measurement needs to be established in terms of its use in follow-up and evaluation of the therapeutic response.
引用
收藏
页码:497 / 503
页数:7
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