<?xml version="1.0"?>
<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.0//EN" "http://www.ncbi.nlm.nih.gov/entrez/query/static/PubMed.dtd">
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Barw</PublisherName>
      <JournalTitle>Barw Medical Journal</JournalTitle>
      <Issn>2960-1959</Issn>
      <PubDate PubStatus="epublish">
        <Year>2025</Year>
        <Month>09</Month>
        <Day>20</Day>
      </PubDate>
    </Journal>
    <ArticleTitle>Emerging Evidence of IgG4-Related Disease in Pericarditis: A Systematic Review</ArticleTitle>
    <FirstPage>45</FirstPage>
    <LastPage>65</LastPage>
    <ELocationID EIdType="doi">10.58742/bmj.vi.204</ELocationID>
    <Language>eng</Language>
    <AuthorList>
      <Author>
        <FirstName EmptyYN="Y"/>
        <LastName>Dilan Hikmat</LastName>
        <Affiliation>Department of Internal Medicine, University of Michigan, Sparrow Hospital, Lansing, Michigan, USA. dilan.sarmad.hiwa@gmail.com</Affiliation>
      </Author>
      <Author>
        <FirstName EmptyYN="Y"/>
        <LastName>Rohan Kumar</LastName>
        <Affiliation>Department of Internal Medicine, University of Michigan, Sparrow Hospital, Lansing, Michigan, USA. Rohan.Kumar@gmail.com</Affiliation>
      </Author>
      <Author>
        <FirstName EmptyYN="Y"/>
        <LastName>Ghasaq Saleh</LastName>
        <Affiliation>Department of Internal Medicine, Michigan State University, Sparrow Hospital, Lansing, Michigan, USA. Ghasaq.Saleh@gmail.com</Affiliation>
      </Author>
      <Author>
        <FirstName EmptyYN="Y"/>
        <LastName>Karam Ghazal-Aswad</LastName>
        <Affiliation>Department of Internal Medicine, University of Michigan, Sparrow Hospital, Lansing, Michigan, USA. Karam.Aswad@gmail.com</Affiliation>
      </Author>
      <Author>
        <FirstName EmptyYN="Y"/>
        <LastName>Mohammad Almasri</LastName>
        <Affiliation>Department of Internal Medicine, Michigan State University, Sparrow Hospital, Lansing, Michigan, USA. Mohammad.Almasri@gmail.com</Affiliation>
      </Author>
      <Author>
        <FirstName EmptyYN="Y"/>
        <LastName>Mohammed Alaa Raslan</LastName>
        <Affiliation>Department of Internal Medicine, University of Michigan, Sparrow Hospital, Lansing, Michigan, USA. Mohammed.Raslan@gmail.com</Affiliation>
      </Author>
      <Author>
        <FirstName EmptyYN="Y"/>
        <LastName>Akhil Gaderaju</LastName>
        <Affiliation>Department of Internal Medicine, Michigan State University, Sparrow Hospital, Lansing, Michigan, USA. Akhil.Gaderaju@gmail.com</Affiliation>
      </Author>
      <Author>
        <FirstName EmptyYN="Y"/>
        <LastName>Adolfo Martinez</LastName>
        <Affiliation>Department of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota, USA. Adolfo.Martinez@gmail.com</Affiliation>
      </Author>
      <Author>
        <FirstName EmptyYN="Y"/>
        <LastName>Saman Al Barznji</LastName>
        <Affiliation>Department of Internal Medicine, Michigan State University, Mclaren Oakland, Pontiac, Michigan, USA. saman.barznji@gmail.com</Affiliation>
      </Author>
      <Author>
        <FirstName EmptyYN="Y"/>
        <LastName>Maitri Shah</LastName>
        <Affiliation>Department of Internal Medicine, Michigan State University, Sparrow Hospital, Lansing, Michigan, USA. Maitri.Shah@gmail.com</Affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2025</Year>
        <Month>07</Month>
        <Day>20</Day>
      </PubDate>
    </History>
    <Abstract>
Introduction


Immunoglobulin G4-related disease (IgG4-RD) is a recently identified immune-mediated condition that is debilitating and often overlooked. While IgG4-RD has been reported in several organs, this study reviews cases where IgG4-RD caused pericarditis.


Methods


A systematic search was conducted from inception until March 1, 2025. All age groups and both sexes with confirmed pericarditis were included, along with the following inclusion criteria: 1) Patients with pericardial biopsy showing IgG4/IgG ratio of &gt;40%. 2) Patients with pericardial biopsy revealing IgG4/HPF of &gt;10. 3) Patients who had confirmed IgG4-RD from other organ biopsies through IgG4 staining, or diagnostic imaging suggestive of IgG4-RD, or pericardial biopsy with classic IgG4-RD histopathologic patterns, with elevated serum IgG4 levels, provided no other diagnosis was more likely.


Results


A total of 50 patients were included, with a mean age of 64.86&#xB1;15.79 years. There were 36 (72%) males. The most common presenting symptom was dyspnea in 27 (54%) patients. Different pericardial involvements were reported, including pericardial thickening 37 (74%), constrictive pericarditis 28 (56%), pericardial effusion 23 (46%), pericardial calcification 6 (12%), and pericardial nodule 5 (10%). In 28 (56%) patients, only the pericardium was affected. In addition to the pericardium, eight (16%) patients had one other organ affected, and 11 (22%) patients had two additional organs affected. Two (4.5%) cases ended in demise.


Conclusion


Although rare, IgG4-RD can cause pericarditis, leading to pericardial thickening, effusion, constrictive pericarditis, or the formation of pericardial nodules. Treatment with corticosteroids or pericardiectomy has been associated with favorable outcomes.
</Abstract>
  </Article>
</ArticleSet>
