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IgG4-positive cell infiltration in various cardiovascular disorders - results from histopathological analysis of surgical samples.

Authors :
Hourai R
Kasashima S
Sohmiya K
Yamauchi Y
Ozawa H
Hirose Y
Ogino Y
Katsumata T
Daimon M
Fujita SI
Hoshiga M
Ishizaka N
Source :
BMC cardiovascular disorders [BMC Cardiovasc Disord] 2017 Feb 03; Vol. 17 (1), pp. 52. Date of Electronic Publication: 2017 Feb 03.
Publication Year :
2017

Abstract

Background: The diagnosis of Immunoglobulin G4 (IgG4)-related disease (IgG4-RD), in general, depends on serum IgG4 concentrations and histopathological findings; therefore, diagnosis of IgG4-RD in cardiovascular organs/tissues is often difficult owing to the risk of tissue sampling.<br />Methods: Prevalence of IgG4-positive lymphoplasmacytic infiltration in 103 consecutive cardiovascular surgical samples from 98 patients with various cardiovascular diseases was analyzed immunohistochemically.<br />Results: The diagnoses of the enrolled patients included aortic aneurysm (abdominal, n = 8; thoracic, n = 9); aortic dissection (n = 20); aortic stenosis (n = 24), aortic regurgitation (n = 10), and mitral stenosis/regurgitation (n = 17). In total, 10 (9.7%) of the 103 specimens showed IgG4-positive cell infiltration with various intensities; five of these were aortic valve specimens from aortic stenosis, and IgG4-positive cell infiltration was present at >10 /HPF in three of them. In one aortic wall sample from an abdominal aortic aneurysm, various histopathological features of IgG4-RD, such as IgG4-positive cell infiltration, obliterating phlebitis, and storiform fibrosis, were observed.<br />Conclusions: IgG4-positive cell infiltration was observed in 9.7% of the surgical cardiovascular specimens, mainly in the aortic valve from aortic stenosis and in the aortic wall from aortic aneurysm. Whether IgG4-positive cell infiltration has pathophysiological importance in the development or progression of cardiovascular diseases should be investigated in future studies.

Details

Language :
English
ISSN :
1471-2261
Volume :
17
Issue :
1
Database :
MEDLINE
Journal :
BMC cardiovascular disorders
Publication Type :
Academic Journal
Accession number :
28158996
Full Text :
https://doi.org/10.1186/s12872-017-0488-3