Autoimmune lymphoproliferative syndrome mimicking chronic active Epstein-Barr virus infection

作者：Nomura Keiko; Kanegane Hirokazu^*; Otsubo Keisuke; Wakiguchi Hiroshi; Noda Yukihiro; Kasahara Yoshihito; Miyawaki Toshio

来源：International Journal of Hematology, 2011, 93(6): 760-764.

DOI：10.1007/s12185-011-0877-9

• Autoimmune lymphoproliferative syndrome
• Chronic active Epstein-Barr virus
• FAS
• IL-10

Chronic active Epstein-Barr virus infection (CAEBV) is defined as a systemic EBV-associated lymphoproliferative disease characterized by fever, lymphadenopathy, and splenomegaly in apparently immunocompetent persons. Recent studies have revealed that EBV infects T or natural killer cells in most patients with CAEBV; the etiology of CAEBV, however, remains unknown. Autoimmune lymphoproliferative disorder (ALPS) is an inherited disorder associated with defects in apoptosis, and clinically characterized by lymphadenopathy, splenomegaly, hypergammaglobulinemia, and autoimmune disease. ALPS is most often associated with mutations in the FAS gene, which is an apoptosis-signaling receptor important for homeostasis of the immune system. Based on the clinical similarity between ALPS and CAEBV with respect to lymphoproliferation, we have examined the possibility of the co-occurrence of ALPS in patients with a diagnosis of CAEBV. In this study, we have identified FAS gene mutations in three Japanese patients with lymphadenopathy, hepatosplenomegaly, and unusual EBV infection, who were diagnosed with CAEBV. These observations, which indicate that the clinical development of ALPS may be associated with EBV infection, alert us to a potential diagnostic pitfall of CAEBV.

• 出版日期2011-6