Chronic active Epstein-Barr virus disease: Difference between revisions
From IDWiki
No edit summary |
No edit summary |
||
Line 22: | Line 22: | ||
=== Related Disorders === |
=== Related Disorders === |
||
==== Severe |
==== Severe Mosquito Bite Sllergy ==== |
||
* A severe hypersensitivity reaction to saliva in the bite of [[Aedes albopictus]] mosquitoes |
* A severe hypersensitivity reaction to saliva in the bite of [[Aedes albopictus]] mosquitoes |
||
Line 29: | Line 29: | ||
* Resoves within a month |
* Resoves within a month |
||
==== Hydroa |
==== Hydroa Vacciniforme ==== |
||
* Characterized by light-induced vesicles |
* Characterized by light-induced vesicles |
Revision as of 15:42, 18 February 2022
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 Sllergy
- 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