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The histological diagnosis of IgG4‐related disease on small biopsies: challenges and pitfalls
Author(s) -
Arora Kshitij,
Rivera Miguel,
Ting David T,
Deshpande Vikram
Publication year - 2019
Publication title -
histopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.626
H-Index - 124
eISSN - 1365-2559
pISSN - 0309-0167
DOI - 10.1111/his.13787
Subject(s) - igg4 related disease , medicine , pathological , immunohistochemistry , pathology , histology , fibrosis , incidence (geometry) , cohort , biopsy , retrospective cohort study , prospective cohort study , stage (stratigraphy) , gastroenterology , biology , paleontology , physics , optics
Aims The pathological diagnosis of IgG4‐related disease (IgG4‐ RD ) relies on histology, IgG4‐positive cells, and an increased IgG4/IgG ratio. Small biopsies from patients with a presumptive diagnosis of IgG4‐ RD often fail to meet consensus histological criteria. The aims of this study were to evaluate consecutive small biopsies from patients with a presumptive diagnosis of IgG4‐ RD , and to assess the significance of the pathological findings. Methods and results We evaluated 55 small biopsies from patients with a presumptive diagnosis of IgG4‐ RD . The retrospective cohort comprised 71 patients with IgG4‐ RD and 57 mimics. We performed immunohistochemistry ( IHC ) and in‐situ hybridisation ( ISH ) for IgG4 and IgG. Twenty‐six patients from the prospective cohort met the histological criteria for IgG4‐ RD (definite); 29 patients lacked one or more pathological features (borderline). Twenty biopsies (36%) lacked both storiform fibrosis and obliterative phlebitis, and nine (16%) lacked an increase in the number of IgG4‐positive plasma cells. Ninety‐three per cent of patients showed an IgG4/total IgG ratio of >40% (>30% by ISH ). There were no differences in the incidence of multiorgan disease ( P = 0.9), serum IgG4 levels ( P = 0.6) and response to therapy between the definite and borderline groups. A strong correlation (Pearson 0.77) between the IHC and ISH platforms was noted with regard to the IgG4/total IgG ratio. Conclusion Patients with a presumptive diagnosis of IgG4‐ RD but lacking the characteristic pathological features of this disease appear to be clinically similar to those who meet the current pathological criteria. An elevated IgG4/total IgG ratio is the most sensitive pathological feature, and ISH provides a robust quantification platform. We recommend evaluating tumefactive lymphoplasmacytic infiltrates with an increased IgG4/IgG ratio, regardless of histological features, for IgG4‐ RD .