| Literature DB >> 27686866 |
Kenji Nishida1, Yuka Sogabe2, Ayako Makihara3, Akemi Senoo3, Hisanori Morimoto4, Mai Takeuchi1, Yuka Gion1, Tadashi Yoshino1, Yasuharu Sato1,5.
Abstract
A 41-year-old man was diagnosed with immunoglobulin G4-related disease (IgG4-RD) in both eyelids 4 years ago and exhibited good response to steroid therapy. However, rapid swelling of the right eyelid lesion was recently observed. As IgG4-RD progression was suspected, biopsy was performed. Although the histology was consistent with IgG4-RD, the infiltrating large atypical lymphoid cells showed immunoglobulin light-chain restriction and IgH gene rearrangement. Consequently, he was diagnosed with extranodal marginal zone lymphoma with abundant IgG4-positive cells.Entities:
Keywords: IgG4-related disease; marginal zone lymphoma; ocular adnexa
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Year: 2016 PMID： 27686866 DOI： 10.1080/14397595.2016.1216733
Source DB: PubMed Journal: Mod Rheumatol ISSN： 1439-7595 Impact factor: 3.023