A Case of Hyper-IgE Syndrome Complicated by Cutaneous, Nodal, and Liver Peripheral T Cell Lymphomas
Author:
Affiliation:
1. Department of Dermatology Asan Medical Center; College of Medicine University of Ulsan; Seoul Korea
Publisher
Wiley
Subject
Dermatology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1346-8138.2002.tb00271.x/fullpdf
Reference6 articles.
1. Hodgkin's disease in a child with hyperimmunoglobulin E syndrome;Lin;Pediatr Hematol Oncol,1998
2. Burkitt's lymphoma developing in a 7-year-old boy with hyper-IgE syndrome;Gorin;J Allery Clin Immunol,1989
3. The hypereosinophilic syndrome associated with CD4+ CD3- helper type 2 (Th2) lymphocytes;Bank;Leuk Lymphoma,2001
4. Medullary CD30+ T cell lymphoma with eosinophilia and hyper IgE supervening during the relentless course of pityriasis lichenoides;Hermanns-Le;Dermatology,2000
5. Immunoregulatory events in the skin of patients with cutaneous T-cell lymphoma;Hansen;Arch Dermatol,1996
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3. Clinical immunology Clinical manifestations in the oral cavity in patients with hyper-IgE syndrome.;Central European Journal of Immunology;2013
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