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Eosinophilic Angiocentric Fibrosis in Bilateral Upper Eyelid Conjunctivas: A First Case Report

Rare disease

Sho Okuyama, Hiroyuki Yazu, Yumi Ito, Hiroshi Minato, Hiroshi Fujishima

Japan Department of Ophthalmology, Keio University Hospital School of Medicine, Tokyo, Japan

Am J Case Rep 2020; 21:e924042

DOI: 10.12659/AJCR.924042

Available online: 2020-04-02

Published: 2020-05-05


#924042

BACKGROUND: Eosinophilic angiocentric fibrosis (EAF) is an extremely rare disease with characteristic histopathological findings of fibrotic onion-skin appearance and eosinophils. The lesion primarily affects the nasal cavity, paranasal sinus, and orbit. Although there have been approximately 78 cases of EAF reported in the literature to date, no cases of EAF in the eyelid conjunctiva have ever been reported.
CASE REPORT: Herein, we describe the case of a 55-year-old Japanese woman with a history of eosinophilic sinusitis and EAF in bilateral upper eyelid conjunctivas who underwent surgical resection of the affected tissue. Histopathological examination revealed collagen bundles winding around the vessels in an onion-skin pattern, and the presence of eosinophils, lymphocytes, and plasma cells.
CONCLUSIONS: We describe the first reported case of EAF in bilateral upper eyelid conjunctivas. It can be successfully treated by surgical resection, and with no recurrence within 6 months postoperatively.

Keywords: Conjunctiva, Eosinophils, Immunohistochemistry, Lymphocytes, Plasma Cells



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