Acquired immune deficiency syndrome in differential diagnosis of hyper-IgE-immunoglobulinemia: Pediatric case report
Date
2017Author
Tamay, Zeynep Ülker
Sutcu, Murat
Torun, Selda
Somer, Ayper
Salman, Nuran
Acar, Manolya
Akturk, Hacer
Umur, Ozge
Metadata
Show full item recordAbstract
Acquired immune deficiency syndrome can be encountered with hypereosinophilia and hyperimmunoglobulin E (hyper-IgE) values, though these levels are rarely so high to be compared with hyperimmunoglobulin E syndrome. A 9-year-old boy presented with the complaint of fatigue, weakness, weight loss and generalized pruritic rash lasting for a year. He had frequent respiratory tract infections, wheezing episodes and urticarial skin lesions before that. On admission, he was cachectic and he had generalized lymphadenopathy, hepatosplenomegaly, oral moniliasis and pruritic rash all over his body. Laboratory evaluation revealed marked lymphopenia and hypergammaglobulinemia with extremely high IgE values (IgE: 59 300 kU/l). He was diagnosed with stage 4 human immunodeficiency virus (HIV) infection and started on antiretroviral treatment. In conclusion, HIV infection can be presented with increased IgE values.
URI
http://hdl.handle.net/20.500.12627/142720https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85014654462&origin=inward
https://doi.org/10.1093/tropej/fmw053
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