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Clinicopathological features of immunoglobulin G4-related constrictive pericarditis.
- Source :
-
Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology [Cardiovasc Pathol] 2024 Sep-Oct; Vol. 72, pp. 107665. Date of Electronic Publication: 2024 May 31. - Publication Year :
- 2024
-
Abstract
- Aim: Constrictive pericarditis (CP) is characterised by scarring fibrosis and a loss of pericardial elasticity, which causes heart failure. IgG4 (immunoglobulin G4)-related disease (IgG4-RD) is a systemic fibro-inflammatory disease characterised by the infiltration of IgG4-immunopositive plasmacytes and high serum IgG4 levels that frequently shape tumorous lesions. Although pericardial involvement of IgG4-RD is rare, with indications of CP, pericardial effusion and irregular masses, the clinical and pathological features remain unclear. In this study, we examined the relationship between CP and IgG4-RD.<br />Methods: Among 35 thick-walled CP cases (histologically pericardial thickening ≥2 mm), eight cases were aetiology identified. Using the diagnostic criteria for IgG4-RD, 11 cases were classified as IgG4-CP, whereas the remainder were considered true idiopathic CP (16 cases) and the clinical pathological features were evaluated.<br />Results: Compared with the other groups, the IgG4-CP group was more common in men and associated with low-grade fever and massive pericardial effusion with frequent recurrence. Deaths resulting from heart failure occurred in a few cases of the IgG4-CP group, but not in other groups. An increase in C-reactive protein and a high positivity rate of anti-nuclear antibodies frequently occurred in the IgG4-CP group. Histologically, the IgG4-CP group included lymphoid follicle, eosinophil infiltration and few calcifications.<br />Conclusions: Pericardial IgG4-RD occurs not only as nodular lesions, but also as thick-walled CP, and accounts for approximately 40% of thick-walled CP cases of unknown cause. The predominant clinical characteristic was refractory and recurrent pericardial effusion. Recognising IgG4-RD as a cause of CP is important to initiate appropriate therapy.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Subjects :
- Humans
Male
Female
Middle Aged
Aged
Adult
Aged, 80 and over
Pericardium pathology
Pericardium immunology
Biomarkers blood
Biomarkers analysis
Recurrence
Retrospective Studies
Fibrosis
Biopsy
Pericarditis, Constrictive pathology
Pericarditis, Constrictive immunology
Immunoglobulin G4-Related Disease pathology
Immunoglobulin G4-Related Disease immunology
Immunoglobulin G4-Related Disease diagnosis
Immunoglobulin G4-Related Disease complications
Immunoglobulin G blood
Pericardial Effusion pathology
Pericardial Effusion immunology
Pericardial Effusion etiology
Subjects
Details
- Language :
- English
- ISSN :
- 1879-1336
- Volume :
- 72
- Database :
- MEDLINE
- Journal :
- Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology
- Publication Type :
- Academic Journal
- Accession number :
- 38825060
- Full Text :
- https://doi.org/10.1016/j.carpath.2024.107665