IgG4-related sclerosing disease encompasses a family of disorders associated with increased numbers of IgG4 plasma cells and mass forming lesions in various tissues. Lymphadenopathy is a common finding, seen in up to 80% of cases. In the largest series of cases to date, we describe histologic, immunohistochemical, special stain and flow cytometric findings in 29 cases of enlarged lymph nodes with increased IgG4 plasma cells. Lymph node biopsies showed all resection specimens; no needle core biopsies of tissue were evaluated. Cases were considered to have increased numbers of IgG4 plasma cells using the histological criteria outlined by Cheuk and Chan (2010): IgG4 plasma cells ≥50 cells in a high-power field and ≥40% of IgG-positive plasma c...
IgG4-related disease (IgG4-RD) is a multisystemic mass forming immune-mediated disease entity, commo...
IgG4 autoimmune disease (or hyper IgG4 disease) is a relatively recently described systemic diseas...
IgG4-related diseases represent a heterogeneous group of conditions characterised by elevated serum ...
OBJECTIVES: IgG4-related disease is a recently recognized condition that can be associated with lymp...
IgG4-related disease is a rare immune-mediated disease that can involve many organs in the body. The...
Progressively transformed germinal centers (PTGC) is a benign process characterised by a morphologic...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
IgG4-related disease (IgG4-RD) is a recently discovered immune-mediated fibroinflammatory condition,...
Background: IgG4-related systemic fibrosclerosis is a recently defined disorder characterised by a d...
Since the earliest reports in 2001, immunoglobulin G4 (IgG4)-related disease has been defined as an ...
Background: Hyalinised fibrous nodules have been encountered within the gastrointestinal tract (GIT)...
Since the first description in the middle of the 1990’s of last century, it has been steadily increa...
Angiofollicular lymph node hyperplasia Clinics and pathology Phenotype/cell stem origin The disease ...
AbstractThe IgG4-related disease (IgG4-RD) is a recurrent chronic fibroinflammatory disease, probabl...
Abstract Background It has been recently accepted that IgG4-related thyroiditis is comparable to the...
IgG4-related disease (IgG4-RD) is a multisystemic mass forming immune-mediated disease entity, commo...
IgG4 autoimmune disease (or hyper IgG4 disease) is a relatively recently described systemic diseas...
IgG4-related diseases represent a heterogeneous group of conditions characterised by elevated serum ...
OBJECTIVES: IgG4-related disease is a recently recognized condition that can be associated with lymp...
IgG4-related disease is a rare immune-mediated disease that can involve many organs in the body. The...
Progressively transformed germinal centers (PTGC) is a benign process characterised by a morphologic...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
IgG4-related disease (IgG4-RD) is a recently discovered immune-mediated fibroinflammatory condition,...
Background: IgG4-related systemic fibrosclerosis is a recently defined disorder characterised by a d...
Since the earliest reports in 2001, immunoglobulin G4 (IgG4)-related disease has been defined as an ...
Background: Hyalinised fibrous nodules have been encountered within the gastrointestinal tract (GIT)...
Since the first description in the middle of the 1990’s of last century, it has been steadily increa...
Angiofollicular lymph node hyperplasia Clinics and pathology Phenotype/cell stem origin The disease ...
AbstractThe IgG4-related disease (IgG4-RD) is a recurrent chronic fibroinflammatory disease, probabl...
Abstract Background It has been recently accepted that IgG4-related thyroiditis is comparable to the...
IgG4-related disease (IgG4-RD) is a multisystemic mass forming immune-mediated disease entity, commo...
IgG4 autoimmune disease (or hyper IgG4 disease) is a relatively recently described systemic diseas...
IgG4-related diseases represent a heterogeneous group of conditions characterised by elevated serum ...