| Literature DB >> 32115519 |
Masashi Funada1, Kazuhisa Nakano1, Hiroko Miyata1, Aya Nawata2, Yoshiya Tanaka1.
Abstract
We herein report a 65-year-old man with elevated serum IgG4 levels, enlarged thyroid, and renal dysfunction, mimicking IgG4-related disease (IgG4-RD). The definitive diagnosis of IgG4-RD was not established because a tissue biopsy revealed no IgG4-positive cell infiltration or fibrosis. The presence of an M peak in the β fraction, Bence Jones protein in urine, and progressive anemia suggested multiple myeloma (MM). The κ/λ ratio was >100, tumor plasma cells were present at >20% in bone marrow, and immunostaining revealed IgG4-positive plasma cells; therefore, he was diagnosed with IgG4-type MM. Patients with elevated IgG4 levels with no significant mass lesions should undergo systemic examinations to exclude malignancy.Entities:
Keywords: IgG4-related disease; IgG4-type multiple myeloma; elevated serum IgG4 level
Year: 2020 PMID: 32115519 DOI: 10.2169/internalmedicine.3839-19
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271