| Literature DB >> 29923967 |
Jung Hyun Lee1, Jeong Hee Kim2, Sang Un Lee1,3, Sung Chul Kim1,3.
Abstract
Kimura disease has been known as a chronic inflammatory disease of unknown etiology, since the first report in 1937 and characterized by an increased eosinophil fraction in peripheral blood, increased serum immunoglobulin E (IgE) levels, and lymphoid granuloma with eosinophilic infiltration on histopathological examination. The authors present a 30-year-old man who visited their clinic with a 3-month history of protrusion and conjunctival injection of the right eye. Surgical mass resection was performed, and initial histopathology revealed Kimura disease. Additional immunohistochemical examination revealed IgG4-related disease in another hospital, which showed more than 80 IgG4-positive plasma cells per high-power field and an IgG4+/IgG+ ratio more than 40%. There are histopathological similarities, and several reports have suggested a relationship between Kimura disease and IgG4-related disease. Thus, it is difficult to classify them as completely different diseases. Kimura disease and IgG4 can be considered a part of a clinical spectrum of abnormal immune reactions.Entities:
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Year: 2018 PMID: 29923967 DOI: 10.1097/IOP.0000000000001135
Source DB: PubMed Journal: Ophthalmic Plast Reconstr Surg ISSN: 0740-9303 Impact factor: 1.746