Rosai-Dorfman Disease in the Breast with Increased IgG4 Expressing Plasma Cells: A Case Report
Â÷À±Áø, ¾ç¿ìÀÍ, ¹Ú¼¼È£, ±¸ÀÚ½Â,
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Â÷À±Áø ( Cha Yoon-Jin )
Yonsei University College of Medicine Department of Pathology
¾ç¿ìÀÍ ( Yang Woo-Ick )
Yonsei University College of Medicine Department of Pathology
¹Ú¼¼È£ ( Park Se-Ho )
Yonsei University College of Medicine Department of Surgery
±¸Àڽ ( Koo Ja-Seung )
Yonsei University College of Medicine Department of Pathology
KMID : 0357920120460050489
Abstract
Rosai-Dorfman disease (RDD) can present in any anatomic site, but breast involvement is rarely reported. Recently, a relationship between RDD and IgG4-related sclerosing disease has been suggested. Here we report another case of RDD with overlapping features of IgG4-related sclerosing disease occurring in a right breast of a 62-year-old female. On microscopic examination, the mass demonstrated a characteristic zonal pattern of proliferation of large polygonal histiocytes and lymphoplasma cells with stromal fibrosis. Emperipolesis was observed in histiocytes with abundant cytoplasm, which showed immunoreactivity for S-100 protein and CD68; the diagnosis of RDD was made. Sheets of plasma cells in the fibrotic stroma demonstrated positive reactions for IgG and IgG4. The mean count of IgG4-positive plasma cells was 100.2/high power field, and the ratio of IgG4/IgG was 56.7%. Additional findings of stromal fibrosis and obliteration of preexisting breast lobules suggested overlapping features with IgG4-related sclerosing disease.
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Breast; Histiocytosis; Immunoglobulin G; Histiocytosis; sinus
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