Tissue-infiltrating immune cells contribute to understanding the pathogenesis of Kimura disease A case report

被引:11
作者
Maehara, Takashi [1 ]
Munemura, Ryusuke [1 ]
Shimizu, Mayumi [2 ]
Kakizoe, Noriko [1 ]
Kaneko, Naoki [3 ]
Murakami, Yuka [1 ]
Masafumi, Moriyama [1 ]
Kiyoshima, Tamotsu [4 ]
Kawano, Shintaro [1 ]
Nakamura, Seiji [1 ]
机构
[1] Kyushu Univ, Sect Oral & Maxillofacial Oncol, Div Maxillofacial Diagnost & Surg Sci, Fac Dent Sci, Fukuoka, Japan
[2] Kyushu Univ, Fac Dent Sci, Dept Oral & Maxillofacial Radiol, Fukuoka, Japan
[3] Harvard Med Sch, Ragon Inst MGH MIT & Harvard, Massachusetts Gen Hosp, Boston, MA 02115 USA
[4] Kyushu Univ, Fac Dent Sci, Div Maxillofacial Diagnost & Surg Sci, Lab Oral Pathol, Fukuoka, Japan
关键词
CD4+T cell; CD4+GATA3+T cell; IgE; Kimura disease; mast cell; T-CELLS;
D O I
10.1097/MD.0000000000018300
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale: Kimura disease (KD) is a rare, chronic inflammatory disorder characterized by subcutaneous granuloma in the head and neck region, as well as increased eosinophil counts and high serum immunoglobulin E (IgE) levels. Kimura disease is suspected to be an IgE-mediated disease, associated with an allergic response, in which antigen-specific B cells are stimulated to undergo specific IgE class switching with disease-specific CD4+ T (Th) cells help. Thus, exploration of the Th cells in affected tissues with KD is a highly promising field of the investigation. However, there have been no reports with direct evidence to implicate Th cells in affected lesions with KD. Here we quantitatively demonstrate that CD4+ GATA3+ T cells and interleukin (IL)-4+ IgE+ c-kit+ mast cells prominently infiltrate in affected lesion with KD. Patient concerns: A 56-year-old Japanese man who exhibited painless swelling in the left parotid region. Diagnoses: Diagnosis of KD was made based on characteristic histopathologic findings, in conjunction with peripheral eosinophilia and elevated serum IgE levels. Interventions: The patient underwent corticosteroid therapy and had been followed for 2 years. Outcomes: We report a rare case of KD of the parotid region in a 56-year-old man, followed by corticosteroid therapy for 2 years. The mass decreased in size and skin itchiness decreased after therapy. He was discharged without any complications. Furthermore, we quantitatively demonstrate the dominance of CD4+ GATA3+ T cells in affected tissues of KD and detect IL-4+ IgE+ c-kit+ mast cells in lesions by multicolor staining approaches. Lessons: The findings from this case suggest that peripheral blood eosinophilia might serve as a marker of recurrent disease, long-term follow-up is necessary due to the possibility of recurrent. Interactions among expanded IgE+ B cells, CD4+ GATA3+ T cells, eosinophils, and activated mast cells might play a critical role in the pathogenesis of KD.
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页数:6
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