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Fulminant hemophagocytic lymphohistiocytosis secondary to a reactivated EBV infection: A case report
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Sciences, Endocrine Tumor Biology.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Radiology, Oncology and Radiation Science, Section of Nuclear Medicine and PET.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Sciences.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Sciences, Rheumatology.
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2013 (English)In: Upsala Journal of Medical Sciences, ISSN 0300-9734, E-ISSN 2000-1967, Vol. 118, no 1, p. 42-45Article in journal (Refereed) Published
Description
Abstract [en]

Hemophagocytic lymphohistiocytosis (HLH) is an aggressive inflammatory syndrome that results from inappropriate activation of the immune system. HLH has a high mortality if not treated. We describe a case of a fulminant HLH, associated with a reactivation of an EBV infection. The patient responded well to steroid treatment.
Place, publisher, year, edition, pages
2013. Vol. 118, no 1, p. 42-45
Keywords [en]
Epstein-Barr, hemophagocytic lymphohistiocytosis, reactivated infection, steroid treatment
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Medical and Health Sciences
Identifiers
URN: urn:nbn:se:uu:diva-196529DOI: 10.3109/03009734.2012.744122ISI: 000314778900008OAI: oai:DiVA.org:uu-196529DiVA, id: diva2:610867
Available from: 2013-03-13 Created: 2013-03-11 Last updated: 2020-08-21Bibliographically approved

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Antonodimitrakis, PantelisWassberg, CeciliaGerovasileiou, SpyridonBack, JohanOlsen, Björn
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Endocrine Tumor BiologySection of Nuclear Medicine and PETDepartment of Medical SciencesRheumatologyInfectious Diseases
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