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Oral ulcerations in a patient with autosomal dominant hyper-IgE syndrome (AD-HIES)

A 23-year-old woman with autosomal dominant hyper-IgE syndrome complicated by recurrent pneumonia and sinusitis presented with 1 week of multiple painful oral ulcers unresponsive to empiric antiviral and antifungal treatment. Her ulcers progressively worsened and she required hospitalisation for int...

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Dettagli Bibliografici
Pubblicato in:BMJ Case Rep
Autori principali: Borst, Johanna, Ma, Lawrence
Natura: Artigo
Lingua:Inglês
Pubblicazione: BMJ Publishing Group 2020
Soggetti:
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7607561/
https://ncbi.nlm.nih.gov/pubmed/33139362
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2020-236705
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