| Literature DB >> 34282558 |
Clayton Bishop1, Alyeesha Wilhelm2, Duncan Watley1, Felix Olobatuyi2, Orly Coblens1, Rohan Joshi3.
Abstract
Kimura disease (KD) is a rare inflammatory disorder which involves the head and neck. Due to its rarity and various findings, definitive diagnosis can be difficult to ascertain. Kimura disease is distinguished from other conditions, including angiolymphoid hyperplasia, by histopathological features including follicular hyperplasia, reactive germinal centers, abundant eosinophilia, eosinophilic microabscesses, preserved nodal architecture, Warthin-Finkeldy polykaryocytes, and capsular fibrosis. Herein, we describe the clinical presentation, pathology, and diagnosis of a single case of a 39-year-old treated at an academic center in Texas.Entities:
Keywords: Angiolymphoid hyperplasia with eosinophilia; Facial mass; Kimura; Kimura disease; Lymphadenopathy; Lymphoid disorders; Neck mass
Mesh:
Year: 2021 PMID: 34282558 PMCID: PMC9018934 DOI: 10.1007/s12105-021-01359-9
Source DB: PubMed Journal: Head Neck Pathol ISSN: 1936-055X