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DOI 10.1016/j.jcv.2009.07.001

Медицинская библиотека · Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology · 2009

Virus-Associated Hemophagocytic Syndrome related to acute CMV and HBV sexual co-infection: a case report.

Halfon Philippe, Retornaz Frederique, Mathieu Didier, Helbert Thierry, Philibert Patrick, Pégliasco Hervé

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Аннотация

BACKGROUND

Secondary or reactive hemophagocytic syndrome is frequently related to viral infections and is named Virus-Associated Hemophagocytic Syndrome (VAHS). Cytomegalovirus (CMV) has been associated with hemophagocytic syndrome in healthy subjects, patients with inflammatory bowel diseases rheumatologic diseases, and transplant recipients. CMV and hepatitis B virus (HBV) can be sexually transmitted. However, co-infection with these viruses has never been reported and the clinical follow-up after acute HBV-CMV infection is not known.

OBJECTIVES

To report on the first case of a VAHS related to acute CMV and HBV co-infection probably acquired after sexual contact.

STUDY

DESIGN

A 47-year-old woman, with no past medical history, complaining of severe asthenia, pneumonia, myalgia, and high fever, was hospitalized for the first time on July 5, 2008. During 20 days, her CMV viral load and HBV DNA were monitored.

RESULTS

Ten days after her hospitalization, all signs and symptoms worsened. Twenty days after hospitalization, the patient had a natural recovery from acute HBV infection and a rapid clearance of CMV infection. Three weeks later, the patient was discharged without any complaints.

CONCLUSION

This report points out the etiological role of CMV and HBV co-infection in VAHS due to probable sexual transmission.

Для цитирования: Halfon Philippe, Retornaz Frederique, Mathieu Didier, Helbert Thierry, Philibert Patrick, Pégliasco Hervé. Virus-Associated Hemophagocytic Syndrome related to acute CMV and HBV sexual co-infection: a case report.. Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology. 2009. DOI: 10.1016/j.jcv.2009.07.001.

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