Publication:
Kimura disease as a rare cause of eosinophil and total IgE elevation

dc.contributor.coauthorTepetam, Fatma Merve
dc.contributor.coauthorOzden, Seyma
dc.contributor.coauthorMersin, Selver Seda
dc.contributor.kuauthorYakut, Tuğçe
dc.contributor.unitKoç University Hospital
dc.date.accessioned2024-12-29T09:36:27Z
dc.date.issued2024
dc.description.abstractKimura disease (KD) is a rare, chronic, inflammatory disorder of unknown etiology characterized by the development of subcutaneous lymphoid masses, usually in the head and neck region; regional lymphadenopathy; peripheral eosinophilia; and elevated levels of serum IgE. KD has been described in China and Japan as "eosinophilic hyperplastic lymphogranuloma" or "atypical granulation associated with hyperplastic abnormalities in the lymphoid tissue". The precise prevalence and incidence and the pathogenesis of KD are unknown. Trauma, infection, an IgE-mediated hypersensitivity reaction, or autoimmune processes have been postulated as possible causes. In this article, we aimed to present a patient who was investigated with elevated serum total IgE and eosinophils and diagnosed as Kimura disease in the light of the current literature.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.issue2
dc.description.publisherscopeInternational
dc.description.volume22
dc.identifier.doi10.21911/aai.2024.457
dc.identifier.issn1308-9234
dc.identifier.quartileQ4
dc.identifier.scopus2-s2.0-85205383267
dc.identifier.urihttps://doi.org/10.21911/aai.2024.457
dc.identifier.urihttps://hdl.handle.net/20.500.14288/22067
dc.identifier.wos1230233300001
dc.keywordsKimura disease
dc.keywordsEosinophilic hyperplastic Lymphogranuloma
dc.languageen
dc.publisherTurkish Natl Soc Allergy and Clinical Immunology
dc.sourceAsthma Allergy Immunology
dc.subjectAllergy
dc.titleKimura disease as a rare cause of eosinophil and total IgE elevation
dc.typeJournal article
dspace.entity.typePublication
local.contributor.kuauthorYakut, Tuğçe

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