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Lymph node granulomas in immunoglobulin G4‐related disease
Author(s) -
Bateman Adrian C,
AshtonKey Margaret R,
Jogai Sanjay
Publication year - 2015
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.12658
Subject(s) - igg4 related disease , pathology , malignancy , plasma cell , context (archaeology) , medicine , lymph node , antibody , differential diagnosis , disease , biology , immunology , bone marrow , paleontology
Aims Immunoglobulin (Ig)G4‐related disease (IgG4‐ RD ) is an increasingly recognized fibroinflammatory condition that commonly exhibits multisystem involvement, with localized (e.g. inflammatory pseudotumours that can mimic malignancy) or diffuse (leading to organ dysfunction) patterns of tissue involvement. The 2012 Boston criteria have standardized the histopathological approach to the diagnosis of IgG4‐ RD and require one or more of the cardinal morphological features with prominence of IgG4 + plasma cells and an IgG4 + /IgG + plasma cell ratio of at least 40%. The relative prevalence of the morphological criteria varies between anatomical sites, but granulomas are rarely found and, indeed, their presence would usually deter a pathologist from making this diagnosis. The aim was to characterize two cases of IgG4‐ RD in which granulomas were present and to highlight this as an unusual feature of the condition. Methods and results We describe two cases in which the features of IgG4‐ RD were present within lymph nodes, together with granulomas. This is a recognized but rare morphological pattern of IgG4‐ RD . Conclusions While an unusual finding, the presence of granulomas should not preclude a diagnosis of IgG4‐ RD in the appropriate clinicopathological context.