Affiliation:
1. Department of Pathology, National Cheng Kung University Hospital, Dou-Liou Branch, College of Medicine, National Cheng Kung University, Yunlin
2. Department of Pathology, National Taiwan University Hospital, College of Medicine, National Taiwan University
3. Department of Pathology, China Medical University Hospital
4. Department of Pathology, Taichung Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Taichung
5. Department of Pathology, National Taiwan University Hospital, Hsin-Chu Branch, Hsin-Chu
6. Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX
7. Department of Pathology, Taipei Tzu-Chi Hospital, Buddhist Tzu Chi Medical Foundation, Taipei
8. Department of Pathology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan
9. Department of Pathology, College of Medicine, Kaohsiung Medical University
10. Department of Pathology, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan
Abstract
Lymphadenopathy with increased immunoglobulin (Ig) G4+ plasma cells can be a nonspecific finding or a manifestation of immunoglobulin G4–related disease (IgG4-RD). It remains unclear whether there are characteristic pathologic features of IgG4-RD involving lymph nodes, or if IgG4-RD lymphadenopathy can occur without other manifestations of IgG4-RD. In this study, we assessed 55 lymph node biopsy specimens (44 men and 11 women with a mean age of 55 y) with increased IgG4+ plasma cells that had 1 of the 6 well-described pathologic patterns. We also correlated these findings with IgG4 serum levels and followed these patients for 7 to 108 months (mean, 34.9 mo) for the occurrence of extranodal IgG4-RD. We further compared lymphadenopathy in patients who developed other manifestations of IgG4-RD (RD+, n=20, 36%) versus those who did not (RD−, n=35, 64%). We found that there were only minor significant differences between 2 groups, including frequency of receiving treatment (RD+, 90% vs. RD−, 60%, P=0.021) and higher serum levels of C-reactive protein (>8 mg/L, RD+, 53% vs. RD−, 13%, P=0.007). Other differences were either borderline or not significant, including mean age (RD+, 59.8 y vs. RD−, 51.9 y, P=0.097), male-to-female ratio (RD+, 16:4 vs. RD−, 28:7, P=1), constitutional symptoms (RD+, 25% vs. RD−, 9%, P=0.096), multiple enlarged lymph nodes (RD+, 45% vs. RD−, 26%, P=0.143), good response to therapy (RD+, 94% vs. RD−, 94%, P=1); higher serum IgG4 levels (>280 mg/dL, RD+, 75% vs. RD−, 51%, P=0.086), anemia (RD+, 45% vs. RD−, 43%, P=0.877), leukopenia (RD+, 0% vs. RD−, 3%, P=0.446), thrombocytopenia (RD+, 10% vs. RD−, 6%, P=0.556), positivity for antinuclear antibody (RD+, 24% vs. RD−, 29%, P=0.688), elevated serum levels of lactate dehydrogenase (>225 U/L, RD+, 0% vs. RD−, 20%, P=0.064), elevated serum IgE level (>100 IU/mL, RD+, 75% vs. RD−, 92%, P=0.238), and hypergammaglobulinemia (RD+, 90% vs. RD−, 86%, P=0.754). There were also no differences in morphologic patterns (P=0.466), IgG4+ cell location (P=0.104), eosinophil counts (RD+, 10.3±11.3 vs. RD−, 13.4±17.5, P=0.496), Epstein-Barr virus positivity (RD+, 35% vs. RD−, 60%, P=0.074), and Epstein-Barr virus–positive cell location (P=0.351). Our findings suggest that there are minimal differences between stringently defined IgG4-RD lymphadenopathy with versus without other manifestations of IgG4-RD. These findings also suggest the existence of IgG4-RD lymphadenopathy as the sole presentation of IgG4-RD.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Pathology and Forensic Medicine,Surgery,Anatomy