Chronic active Epstein-Barr virus disease: Difference between revisions

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== Background ==
==Background==


* Life-threatening infection with [[Epstein-Barr virus]] involving NK and T cells
*Life-threatening inflammatory disorder and lymphoid neoplasm caused by infection with [[Epstein-Barr virus]] involving NK and T cells


=== Pathophysiology ===
===Pathophysiology===


* EBV infection involving B, T, or NK cells
*EBV infection involving B, T, and/or NK cells


=== Epidemiology ===
===Epidemiology===


* Most cases reported in people of Asian and North American Indigenous descent
*Most cases reported in Japan and East Asia
* Most common in Japan
*In the Americas, more common in Indigenous populations
*However, can occur in people of all ethnicities


== Clinical Manifestations ==
==Clinical Manifestations==


*Symptoms include fever, liver dysfunction, [[splenomegaly]], [[lymphadenopathy]], and [[thrombocytopenia]]
*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]]
*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]]
*Occasionally has [[uveitis]], CNS disease, intestinal perforation, and [[myocarditis]]
*Can progress to frank [[lymphoma]] or [[hemophagocytic lymphohistiocytosis]]


== Management ==
=== Related Disorders ===


==== Severe mosquito bite allergy ====
* [[Hematopoietic stem cell transplantation]] is the only curative treatment

* Symptoms may be temporarily improved with [[corticosteroids]]
* 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 [[Infectious mononucleosis|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 (>10<sup>2.5</sup> 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 ≥10<sup>2.5</sup> copies/μg DNA
** Detection of EBV infection of T or NK cells in affected tissues or peripheral blood

==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: [https://doi.org/10.3389/fped.2019.00014 10.3389/fped.2019.00014]


[[Category:Hematology]]
[[Category:Hematology]]

Revision as of 01:34, 16 October 2020

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

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

Management

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