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1000 Titel
  • Recurrent parvovirus B19 viremia resulting in two episodes of hemophagocytic lymphohistiocytosis
1000 Autor/in
  1. Orth, Hans Martin |
  2. Fuchs, Andre |
  3. Lübke, Nadine |
  4. Jensen, Björn-Erik Ole |
  5. Luedde, Tom |
1000 Verlag BioMed Central
1000 Erscheinungsjahr 2022
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2022-06-25
1000 Erschienen in
1000 Quellenangabe
  • 19(1):107
1000 Copyrightjahr
  • 2022
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s12985-022-01841-y |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233783/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:sec> <jats:title>Background</jats:title> <jats:p>Hemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory condition with uncontrolled activation of lymphocytes and macrophages. Besides a primary (genetic) form, HLH can also be triggered by malignant, autoimmune and infectious diseases. HLH recurrences are rarely described, usually only in primary HLH. <jats:italic>Parvovirus B19</jats:italic> (PVB19) Infection is one of the rare and rather benign causes of HLH. Since the infection usually results in long-lasting immunity, recurrent viremia is very uncommon. </jats:p> </jats:sec><jats:sec> <jats:title>Case presentation</jats:title> <jats:p>We report an unusual case of a young female with recurrent PVB19 infection that led to repeated episodes of HLH. The first episode occurred at the age of 25 years with a three-week history of high fever and nonspecific accompanying symptoms. The diagnosis of HLH was confirmed by HLH-2004 criteria and HScore, PVB19 viremia was detected as underlying cause. Following guideline-based therapy, the patient was symptom-free for one year, before similar symptoms recurred in a milder form. Again, PVB19 was detected and HLH was diagnosed according to HScore. After successful treatment and a nine-month symptom-free interval, a third phase of hyperinflammation with low PVB19 viremia occurred; this time, treatment with a corticosteroid and intravenous immunoglobulin was initiated before the presence of clear diagnostic criteria for HLH. No further events occurred in the following three years.</jats:p> </jats:sec><jats:sec> <jats:title>Conclusions</jats:title> <jats:p>In the case of our patient, the recurrent viremia triggered three episodes of hyperinflammation, two of which were clearly diagnosed as HLH. To our knowledge, this is the first published case of recurrent HLH due to PVB19 infection. Therefore, the case gives new insights in triggering mechanisms for HLH. </jats:p> </jats:sec>
1000 Sacherschließung
lokal Female [MeSH]
lokal Adult [MeSH]
lokal Humans [MeSH]
lokal Clinical Virology
lokal Parvovirus B19, Human [MeSH]
lokal Macrophage activation syndrome
lokal Lymphohistiocytosis, Hemophagocytic/drug therapy [MeSH]
lokal Lymphohistiocytosis, Hemophagocytic/diagnosis [MeSH]
lokal Medical and Health Sciences
lokal HLH
lokal HScore
lokal Relapse
lokal Viremia/diagnosis [MeSH]
lokal Case Report
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  1. https://orcid.org/0000-0003-3053-6730|https://frl.publisso.de/adhoc/uri/RnVjaHMsIEFuZHJl|https://frl.publisso.de/adhoc/uri/TMO8YmtlLCBOYWRpbmU=|https://frl.publisso.de/adhoc/uri/SmVuc2VuLCBCasO2cm4tRXJpayBPbGU=|https://frl.publisso.de/adhoc/uri/THVlZGRlLCBUb20=
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  1. Universitätsklinikum Düsseldorf. Anstalt öffentlichen Rechts |
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    1000 Förderer Universitätsklinikum Düsseldorf. Anstalt öffentlichen Rechts |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 Erstellt am 2024-10-02T17:51:35.682+0200
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