Kimura Disease Presenting with Buccal Mass: A Case Report and Literature Review

被引:0
|
作者
Ryosuke Sato
Nobuyuki Bandoh
Takashi Goto
Haruyuki Ichikawa
Akihiro Uemura
Shiori Suzuki
Tomomi Yamaguchi
Eriko Aimono
Hiroshi Nishihara
Akihiro Katada
Yasuaki Harabuchi
机构
[1] Hokuto Hospital,Department of Otolaryngology
[2] Asahikawa Medical University,Head and Neck Surgery
[3] Hokuto Hospital,Department of Otolaryngology
[4] Keio University School of Medicine,Head and Neck Surgery
来源
Head and Neck Pathology | 2021年 / 15卷
关键词
Kimura disease; Buccal mass; Eosinophil; Immunoglobulin E; Steroid;
D O I
暂无
中图分类号
学科分类号
摘要
A 52-year-old man with a 2-year history of left buccal swelling was admitted to our department. An elastic hard oral mass was palpated under the intact buccal mucosa. A CT scan with enhancement revealed a solid mass measuring 2.0 × 1.5 × 1.3 cm between the left masseter muscle and the maxilla. Laboratory examination showed elevated peripheral blood eosinophil count of 1070/μL (12.3%) and serum immunoglobulin (Ig)E level of 1374 IU/mL. Histologic examination of transorally excised mass revealed lymphoid follicular hyperplasia with reactive germinal centers and eosinophilic infiltration with eosinophilic micro-abscesses in the germinal centers. Abundant IgE deposition in a reticular fashion was observed in the germinal centers and c-kit positive mast cells was observed in the paracortical area in the excised mass. The patient was diagnosed with Kimura disease (KD) and treated with oral prednisolone, tapering from 10 mg/day for approximately 8 months. Eosinophil count and serum IgE level decreased to 435/μL (5%) and 520 IU/dL, respectively. He is free from symptoms at the time of this submission. KD, a rare, benign, and chronic inflammatory disorder, occurs predominantly in young male adults in Asia. Patients with KD who presents with buccal mass are relatively rare. Immunohistologic analyses suggested that an allergic reaction played an important role in the etiology of KD in this case.
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页码:657 / 662
页数:5
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