IgG4-related disease presenting with inflammatory pseudotumor of the buccal submucosa: A case report

被引:1
|
作者
Kobashi, H. [1 ]
Ishii, S. [1 ]
Yakushiji, N. [1 ]
机构
[1] Kinki Cent Hosp, Dept Oral & Maxillofacial Surg, Itami, Hyogo, Japan
关键词
Inflammatory pseudotumor (IPT); Immunoglobulin G4-related disease (IgG4-RD); IgG4-positive plasma cells;
D O I
10.1016/j.ajoms.2017.11.005
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Inflammatory pseudotumor is a rare clinical condition that may be associated with immunoglobulin G4-related disease. However, conclusive etiological links with immunoglobulin G4-related disease have not been identified in the few reported cases of oral inflammatory pseudotumors. We describe a case of an inflammatory pseudotumor of the buccal submucosa that was histopathologically confirmed to be a manifestation of immunoglobulin G4-related disease. The patient was an 83-year-old man who visited our department for the examination of swelling in the left buccal mucosa. The initial examination identified a painless, movable tumor with a long axis (approximately 40 mm) on the left buccal submucosa. Biopsy, magnetic resonance imaging, and computed tomographic findings did not clearly indicate malignancy, and the tumor was excised to facilitate a confirmative diagnosis. Histopathological examination revealed inflammatory cell infiltration of the adipose tissue as well as many lymphoid follicles. Immunohistochemistry predominantly revealed immunoglobulin G4-related disease-positive cells, thereby confirming the diagnosis of immunoglobulin G4-related disease. However, a postoperative blood test revealed normal immunoglobulin G4 levels, and steroid therapy was not initiated. The patient remains symptom- and recurrence-free at 18 months after surgery. (C) 2017 Asian AOMS, ASOMP, JSOP, JSOMS, JSOM, and JAMI. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:166 / 168
页数:3
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