The Clinical Utility of Autoantibodies in Patients with Idiopathic Granulomatous Mastitis

Background Although the etiopathogenesis of idiopathic granulomatous mastitis (IGM) is still controversial, recently autoimmunity and immune dysregulation have been emphasized. The aim of this study is to investigate the clinical utility of autoantibodies in IGM. Material and Methods Rheumatoid fact...

Full description

Bibliographic Details
Main Author: Hande Koksal
Format: Article
Language:English
Published: Taylor & Francis Group 2022-02-01
Series:Journal of Investigative Surgery
Subjects:
Online Access:http://dx.doi.org/10.1080/08941939.2020.1861666
_version_ 1797684500019281920
author Hande Koksal
author_facet Hande Koksal
author_sort Hande Koksal
collection DOAJ
description Background Although the etiopathogenesis of idiopathic granulomatous mastitis (IGM) is still controversial, recently autoimmunity and immune dysregulation have been emphasized. The aim of this study is to investigate the clinical utility of autoantibodies in IGM. Material and Methods Rheumatoid factor (RF), antinuclear antibody (ANA), anti-double stranded DNA antibody (anti-ds-DNA), anti-cyclic citrullinated peptides antibody (anti-CCP) and perinuclear anti-neutrophil cytoplasmic antibody (pANCA) levels were investigated in pathologically diagnosed IGM patients (Group IGM) and healthy women (Group C). IGM patients were divided into two groups as those with active symptoms and signs (Group IGMA) and those without clinical and radiological findings (Group IGMR). Results While, in Group IGM, the positivity of RF, ANA, anti-ds-DNA, pANCA and anti-CCP was 13.1%, 3.3%, 1.6%, 0%, and 3.3%, respectively, in Group C, they were 13.3%, 0%, 0%, 0%, and 0%, respectively. The differences were not statistically significant (p > .05). In Groups IGMA, IGMR and C, RF positivity was 10%, 16.1%, and 13.3%, respectively. The ANA positivity of Groups IGMA, IGMR and C was 0%, 6.5%, and 0%, respectively. Groups IGMA, IGMR and C’s anti-ds-DNA positivity were 0%, 3.2%, and 0%, respectively. In all groups, pANCA was negative. The anti-CCP positivity of Groups IGMA, IGMR and C was 6.7%, 0%, and 0%, respectively. Conclusion Our findings did not support the clinical utility of autoantibodies including RF, ANA, anti-ds-DNA, pANCA and anti-CCP in IGM.
first_indexed 2024-03-12T00:31:37Z
format Article
id doaj.art-cb9213aa66e3404f939570e39ebf3390
institution Directory Open Access Journal
issn 0894-1939
1521-0553
language English
last_indexed 2024-03-12T00:31:37Z
publishDate 2022-02-01
publisher Taylor & Francis Group
record_format Article
series Journal of Investigative Surgery
spelling doaj.art-cb9213aa66e3404f939570e39ebf33902023-09-15T10:21:27ZengTaylor & Francis GroupJournal of Investigative Surgery0894-19391521-05532022-02-0135232532910.1080/08941939.2020.18616661861666The Clinical Utility of Autoantibodies in Patients with Idiopathic Granulomatous MastitisHande Koksal0Department of General Surgery, Saglik Bilimleri University, Hamidiye Faculty of Medicine, Ministry of Health Konya City HospitalBackground Although the etiopathogenesis of idiopathic granulomatous mastitis (IGM) is still controversial, recently autoimmunity and immune dysregulation have been emphasized. The aim of this study is to investigate the clinical utility of autoantibodies in IGM. Material and Methods Rheumatoid factor (RF), antinuclear antibody (ANA), anti-double stranded DNA antibody (anti-ds-DNA), anti-cyclic citrullinated peptides antibody (anti-CCP) and perinuclear anti-neutrophil cytoplasmic antibody (pANCA) levels were investigated in pathologically diagnosed IGM patients (Group IGM) and healthy women (Group C). IGM patients were divided into two groups as those with active symptoms and signs (Group IGMA) and those without clinical and radiological findings (Group IGMR). Results While, in Group IGM, the positivity of RF, ANA, anti-ds-DNA, pANCA and anti-CCP was 13.1%, 3.3%, 1.6%, 0%, and 3.3%, respectively, in Group C, they were 13.3%, 0%, 0%, 0%, and 0%, respectively. The differences were not statistically significant (p > .05). In Groups IGMA, IGMR and C, RF positivity was 10%, 16.1%, and 13.3%, respectively. The ANA positivity of Groups IGMA, IGMR and C was 0%, 6.5%, and 0%, respectively. Groups IGMA, IGMR and C’s anti-ds-DNA positivity were 0%, 3.2%, and 0%, respectively. In all groups, pANCA was negative. The anti-CCP positivity of Groups IGMA, IGMR and C was 6.7%, 0%, and 0%, respectively. Conclusion Our findings did not support the clinical utility of autoantibodies including RF, ANA, anti-ds-DNA, pANCA and anti-CCP in IGM.http://dx.doi.org/10.1080/08941939.2020.1861666rheumatoid factorantinuclear antibody anti-double stranded dna antibodyanti-cyclic citrullinated peptides antibodyperinuclear anti-neutrophil cytoplasmic antibodyidiopathic granulomatous mastitis
spellingShingle Hande Koksal
The Clinical Utility of Autoantibodies in Patients with Idiopathic Granulomatous Mastitis
Journal of Investigative Surgery
rheumatoid factor
antinuclear antibody
anti-double stranded dna antibody
anti-cyclic citrullinated peptides antibody
perinuclear anti-neutrophil cytoplasmic antibody
idiopathic granulomatous mastitis
title The Clinical Utility of Autoantibodies in Patients with Idiopathic Granulomatous Mastitis
title_full The Clinical Utility of Autoantibodies in Patients with Idiopathic Granulomatous Mastitis
title_fullStr The Clinical Utility of Autoantibodies in Patients with Idiopathic Granulomatous Mastitis
title_full_unstemmed The Clinical Utility of Autoantibodies in Patients with Idiopathic Granulomatous Mastitis
title_short The Clinical Utility of Autoantibodies in Patients with Idiopathic Granulomatous Mastitis
title_sort clinical utility of autoantibodies in patients with idiopathic granulomatous mastitis
topic rheumatoid factor
antinuclear antibody
anti-double stranded dna antibody
anti-cyclic citrullinated peptides antibody
perinuclear anti-neutrophil cytoplasmic antibody
idiopathic granulomatous mastitis
url http://dx.doi.org/10.1080/08941939.2020.1861666
work_keys_str_mv AT handekoksal theclinicalutilityofautoantibodiesinpatientswithidiopathicgranulomatousmastitis
AT handekoksal clinicalutilityofautoantibodiesinpatientswithidiopathicgranulomatousmastitis