ArticleIDCases2025
Fulminant disseminated human parvovirus B19 infection: Case report.
Article in IDCases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Fulminant, disseminated Human parvovirus B19 (HPV B19) infection is uncommon and can be fatal if unrecognized. Case presentation: A 35-year-old man developed abrupt confusion on the second day of incarceration. He was admitted to intensive care with acute kidney, liver injury, coagulopathy, thrombocytopenia, and persistent hematochezia. The etiology remained unclear until next-generation sequencing detected HPV B19 DNA in blood, cerebrospinal fluid (CSF), bronchoalveolar lavage fluid, and ascitic fluid. On illness Day 32, B19 infection was confirmed by quantitative PCR from blood, CSF, and a rectal biopsy. Despite negative B19-specific IgM, the patient improved after four weeks of supportive care and two courses of intravenous immunoglobulin, with recovery of renal, hepatic, and respiratory function and resolution of rectal lesions. Conclusions: Disseminated HPV B19 infection should be considered in unexplained multiorgan dysfunction, even in the absence of rash or IgM seroconversion. Early PCR-based testing of blood and affected tissues can be diagnostic.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.