Sjögren’s syndrome–associated fulminant myocarditis presenting as cardiogenic shock requiring VA-ECMO: a case report

Fulminant autoimmune myocarditis is a rare but life-threatening condition that can present as the initial manifestation of an underlying autoimmune disease. Early recognition and prompt initiation of mechanical circulatory support and immunosuppressive therapy are critical for survival. We report the case of a previously healthy young woman who presented with acute cardiogenic shock following a syncopal episode and rapidly progressive dyspnea. Initial investigations ruled out ischemic, infectious, and toxicologic causes. Coronary angiography revealed normal coronary arteries. She developed sustained ventricular arrhythmias and severe left ventricular dysfunction (ejection fraction 10–15%), requiring urgent Veno arterial extracorporeal membrane oxygenation (VA-ECMO) support. Immunologic testing revealed a positive antinuclear antibody (ANA) by ELISA (> 400 AU/mL), strongly positive anti-SSA (Ro) antibodies, and borderline anti-SSB antibodies, raising suspicion for Sjogren syndrome–associated myocarditis. High-dose intravenous methylprednisolone therapy was initiated, leading to rapid clinical improvement, with successful ECMO weaning after four days. Follow-up echocardiography showed normalization of left ventricular function. Cardiac MRI confirmed myocarditis according to the updated Lake Louise criteria. At one-year follow-up, the patient demonstrated full cardiac recovery and was diagnosed with Sjogren’s syndrome. This case highlights the importance of early recognition, aggressive immunosuppression, and mechanical circulatory support in fulminant autoimmune myocarditis. It also underscores the value of long-term follow-up for confirming underlying systemic autoimmune diseases, which may initially present with isolated cardiac involvement. Comprehensive autoimmune evaluation should be considered in young patients with unexplained fulminant myocarditis, especially females, to enable timely diagnosis and tailored immunosuppressive therapy.

Authors

Institutions

Publication Details

Journal
BMC Cardiovascular Disorders
Published
2025-10-27
DOI
https://doi.org/10.1186/s12872-025-05106-8
Primary Topic
Viral Infections and Immunology Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Sjögren’s syndrome–associated fulminant myocarditis presenting as cardiogenic shock requiring VA-ECMO: a case report

Quoc Thang Le, Ting Ai, Sinh Hien Nguyen, Thanh Hoa Tran
BMC Cardiovascular Disorders
Viral Infections and Immunology Research
article

Sjögren’s syndrome–associated fulminant myocarditis presenting as cardiogenic shock requiring VA-ECMO: a case report

Quoc Thang Le, Ting Ai, Sinh Hien Nguyen, Thanh Hoa Tran
article en

Abstract

Fulminant autoimmune myocarditis is a rare but life-threatening condition that can present as the initial manifestation of an underlying autoimmune disease. Early recognition and prompt initiation of mechanical circulatory support and immunosuppressive therapy are critical for survival. We report the case of a previously healthy young woman who presented with acute cardiogenic shock following a syncopal episode and rapidly progressive dyspnea. Initial investigations ruled out ischemic, infectious, and toxicologic causes. Coronary angiography revealed normal coronary arteries. She developed sustained ventricular arrhythmias and severe left ventricular dysfunction (ejection fraction 10–15%), requiring urgent Veno arterial extracorporeal membrane oxygenation (VA-ECMO) support. Immunologic testing revealed a positive antinuclear antibody (ANA) by ELISA (> 400 AU/mL), strongly positive anti-SSA (Ro) antibodies, and borderline anti-SSB antibodies, raising suspicion for Sjogren syndrome–associated myocarditis. High-dose intravenous methylprednisolone therapy was initiated, leading to rapid clinical improvement, with successful ECMO weaning after four days. Follow-up echocardiography showed normalization of left ventricular function. Cardiac MRI confirmed myocarditis according to the updated Lake Louise criteria. At one-year follow-up, the patient demonstrated full cardiac recovery and was diagnosed with Sjogren’s syndrome. This case highlights the importance of early recognition, aggressive immunosuppression, and mechanical circulatory support in fulminant autoimmune myocarditis. It also underscores the value of long-term follow-up for confirming underlying systemic autoimmune diseases, which may initially present with isolated cardiac involvement. Comprehensive autoimmune evaluation should be considered in young patients with unexplained fulminant myocarditis, especially females, to enable timely diagnosis and tailored immunosuppressive therapy.

BMC Cardiovascular DisordersVol. 25(1)
VinUniversity (VN), VNU University of Science (VN)
Openalex Percentile: Top 53%
Viral Infections and Immunology Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.