A case of pure red cell aplasia and systemic lupus erythematosus caused by human parvovirus B19 infection
Rheumatology International, ISSN: 0172-8172, Vol: 27, Issue: 4, Page: 411-414
2007
- 20Citations
- 11Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations20
- Citation Indexes20
- 20
- CrossRef12
- Captures11
- Readers11
- 11
Article Description
Human parvovirus B19 (B19) rarely induces pure red cell aplasia (PRCA) in healthy hosts. Meanwhile B19 infection is often clinically similar to systemic lupus erythematosus (SLE), and several cases have been reported wherein B19 actually stimulated SLE exacerbation in an immunocompetent subject. An 82-year-old healthy woman was diagnosed to have complicated with B19 infection and PRCA. Four weeks later, she had high fever, polyarthritis, and oral ulcers, additionally diagnosed with SLE, and subsequently, 15 mg of prednisone was started. This is the first case wherein B19 infection caused both PRCA and SLE in a healthy patient as far as our investigations are concerned. © 2006 Springer-Verlag.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=33846314013&origin=inward; http://dx.doi.org/10.1007/s00296-006-0227-z; http://www.ncbi.nlm.nih.gov/pubmed/17028860; http://link.springer.com/10.1007/s00296-006-0227-z; https://dx.doi.org/10.1007/s00296-006-0227-z; https://link.springer.com/article/10.1007/s00296-006-0227-z; http://www.springerlink.com/index/10.1007/s00296-006-0227-z; http://www.springerlink.com/index/pdf/10.1007/s00296-006-0227-z
Springer Science and Business Media LLC
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