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Multiple and Persistent Viral Infections in a Patient With Bare Lymphocyte Syndrome
Bare lymphocyte syndrome (BLS), first described by Schuurman et al. and Touraine et al., is characterized by the lack of expression of class I and/or II HLA antigens and beta -microglobulin on lymphocytes, an occurrence resulting in a form of partial combined immunodeficiency (CID). Clinical manifes...
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Published in: | The Journal of infectious diseases 1987-11, Vol.156 (5), p.837-840 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Bare lymphocyte syndrome (BLS), first described by Schuurman et al. and Touraine et al., is characterized by the lack of expression of class I and/or II HLA antigens and beta -microglobulin on lymphocytes, an occurrence resulting in a form of partial combined immunodeficiency (CID). Clinical manifestations have included oral candidiasis, Pneumocystis carinii and bacterial pneumonias, diarrhea resulting in growth failure, septicemia, and viral infections. In this report, the authors describe the clinical diagnosis and hospital course of a Caucasian infant of Irish and English descent with BLS who had multiple and simultaneous viral infections. He was treated with high-dose, intravenous gammaglobulin (IVIG) in attempts to contain infections with multiple enteroviruses, rhinovirus, and two serotypes of adenovirus. |
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ISSN: | 0022-1899 1537-6613 |
DOI: | 10.1093/infdis/156.5.837 |