Chronic active Epstein-Barr virus disease
From IDWiki
Background
- Life-threatening inflammatory disorder and lymphoid neoplasm caused by infection with Epstein-Barr virus involving NK and T cells
Pathophysiology
- EBV infection involving B, T, and/or NK cells
Epidemiology
- Most cases reported in Japan and East Asia
- In the Americas, more common in Indigenous populations
- However, can occur in people of all ethnicities
Clinical Manifestations
- Symptoms include fever, liver dysfunction, splenomegaly, lymphadenopathy, and thrombocytopenia
- May also have hepatomegaly, anemia, mosquito bite hypersensitivity, rashes, oral ulcers, hemophagocytic lymphohistiocytosis, coronary artery aneurysm, liver failure, lymphoma, and interstitial pneumonia
- Occasionally has uveitis, CNS disease, intestinal perforation, and myocarditis
- Can progress to frank lymphoma or hemophagocytic lymphohistiocytosis
Related Disorders
Severe mosquito bite allergy
- A severe hypersensitivity reaction to saliva in the bite of Aedes albopictus mosquitoes
- Characterized by local skin inflammation followed by high fever, lymphadenopathy, and liver dysfunction
- The bite can ulcerate and scar
- Resoves within a month
Hydroa vacciniforme
- Characterized by light-induced vesicles
- Can also involve systemic inflammation
Diagnostic Criteria
- Sustained or recurrent IM‐like symptoms for greater than 3 months
- Symptoms include fever, lymphadenopathy, and hepatosplenomegaly, and possibly other symptoms
- Elevated EBV genome load in the peripheral blood (>102.5 copies/µg DNA)
- EBV infection of T or NK cells in the affected tissues or peripheral blood
- Exclusion of other possible diagnoses including the following:
- Primary EBV infection (infectious mononucleosis)
- Primary immunodeficiencies
- HIV
- Iatrogenic immunosuppression
- Autoimmune or collagen vascular diseases
- Other malignant lymphoma (classic Hodgkin lymphoma, extranodal NK/T cell lymphoma, including nasal type, peripheral T cell lymphomas, and aggressive NK‐cell leukemia)
Diagnosis
- Can follow a series of stepwise diagnostic tests:
- Anti-EBV antibodies demonstrating anti-VCA-IgG (necessary for diagnosis), anti-EA-IgG, and anti-VCA-IgA or anti-EA-IgA antibodies
- Anti-EBNA antibodies may be negative
- EBV DNA viral load ≥102.5 copies/μg DNA
- Detection of EBV infection of T or NK cells in affected tissues or peripheral blood
- Anti-EBV antibodies demonstrating anti-VCA-IgG (necessary for diagnosis), anti-EA-IgG, and anti-VCA-IgA or anti-EA-IgA antibodies
Management
- Hematopoietic stem cell transplantation is the only curative treatment
- Symptoms may be temporarily improved with corticosteroids
Further Reading
- Advances in the Study of Chronic Active Epstein-Barr Virus Infection: Clinical Features Under the 2016 WHO Classification and Mechanisms of Development. Front Pediatr. 2019;7:14. doi: 10.3389/fped.2019.00014
References
- ^ Hiroshi Kimura, Yo Hoshino, Hirokazu Kanegane, Ikuya Tsuge, Takayuki Okamura, Keisei Kawa, Tsuneo Morishima. Clinical and virologic characteristics of chronic active Epstein-Barr virus infection. Blood. 2001;98(2):280-286. doi:10.1182/blood.v98.2.280.
- ^ Jeffrey I. Cohen, Elaine S. Jaffe, Janet K. Dale, Stefania Pittaluga, Helen E. Heslop, Cliona M. Rooney, Stephen Gottschalk, Catherine M. Bollard, V. Koneti Rao, Adriana Marques, Peter D. Burbelo, Siu-Ping Turk, Rachael Fulton, Alan S. Wayne, Richard F. Little, Mitchell S. Cairo, Nader K. El-Mallawany, Daniel Fowler, Claude Sportes, Michael R. Bishop, Wyndham Wilson, Stephen E. Straus. Characterization and treatment of chronic active Epstein-Barr virus disease: a 28-year experience in the United States. Blood. 2011;117(22):5835-5849. doi:10.1182/blood-2010-11-316745.
