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An Efficient and Simple Method to Establish NK and T Cell Lines from Patients with Chronic Active Epstein-Barr Virus Infection
Published on: March 30, 2018
[Chronic active Epstein-Barr virus infection in an adult]
1Instytucie Hematologii i Transfuzjologii w Warszawie. jkoscielak@ihit.waw.pl
Insights
This case report details a rare chronic active Epstein-Barr virus infection (CAEBV) in an older Caucasian woman. Early diagnosis and steroid therapy were crucial for recovery from this severe infectious mononucleosis complication.
Area of Science:
- Infectious Diseases
- Virology
- Immunology
Background:
- Chronic active Epstein-Barr virus infection (CAEBV) is a rare but severe complication of infectious mononucleosis.
- Diagnosis can be delayed, particularly in Caucasian populations and older individuals, due to low prevalence and atypical presentations.
Observation:
- A 58-year-old woman presented with prolonged symptoms including intermittent fever, lymphadenopathy, and splenomegaly.
- Diagnosis was delayed by eight months, with initial treatment involving high-dose methylprednisolone showing significant but temporary improvement.
Findings:
- Epstein-Barr virus (EBV) infection was confirmed by elevated antibodies (VCA, EA, EBNA) and detectable EBV DNA in blood and saliva.
- The patient experienced a full recovery after one year of management, with a milder disease course after initial steroid therapy.
Implications:
- This case highlights the importance of considering CAEBV in older adults presenting with prolonged infectious mononucleosis-like symptoms.
- Successful steroid therapy suggests a potential role for immunomodulation in managing CAEBV, warranting further investigation.
- Understanding CAEBV's link to lymphoproliferative disorders is critical for comprehensive patient care.
Abstract:
A chronic active Epstein-Barr virus infection (CAEBV) following infectious mononucleosis in a 58 years old woman is reported. The disease lasted for one year, and in spite of an intensive search for its cause, was diagnosed only at the 8th months since its onset. A low frequency of CAEBV in caucasians and patient's age were likely responsible for the belated diagnosis. The disease presented with a high, intermittent fever, general lymphoadenopathy, splenomegalia, hypoalbuminemia, polyclonal gamma globulinemia and malaise. Starting from the 6th month, i.e. before the diagnosis was established, a high dose oral therapy with methylprednisolone was introduced. The improvement was significant but the disease recurred after drug withdrawal. Nevertheless its course was milder. At the 8th month since the disease onset elevated antibody to viral capsid antigen (VCA) together with antibody to early antigen (EA) and nuclear antigen (EBNA) were still found in patient's blood. DNA of EBV was detected by PCR in patient's blood and saliva. The patient recovered completely after one year, and as of today i.e. June 2009, is feeling well. A likely cause of the successful steroid therapy is discussed. A review part of the article describes etiopathogenesis, complications, occurrence and treatment of CAEBV, as well as its relation to various lymphoproliferation disorders.
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