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We present a case of newly diagnosed heart failure with reduced ejection fraction secondary to antisynthetase syndrome (ATS) in a 63-year-old female patient. The patient presented with symptoms and laboratory findings indicative of an ATS flare, which included inflammatory arthritis, muscular involvement, and exertional dyspnea. A systematic and structured diagnostic approach was undertaken, commencing with transthoracic echocardiography (TTE) to evaluate cardiac function and morphology. This was followed by ischemic assessment through coronary angiography to rule out ischemic heart disease, and subsequently, cardiac magnetic resonance imaging (CMR) based on findings from the TTE. The initial TTE revealed a newly reduced ejection fraction of 30-35%, a significant decline from previous normal echocardiograms. The ischemic evaluation identified mild, non-obstructive coronary artery disease, effectively excluding ischemic cardiomyopathy as a contributing factor. CMR was pursued due to concerns for myocarditis and provided further diagnostic clarity, revealing impaired left ventricular (LV) systolic function and near-transmural late gadolinium enhancement (LGE) in the inferolateral and anterolateral wall segments, along with subendocardial LGE in the inferoseptal wall segment. These findings were consistent with regional wall motion abnormalities observed on TTE. In response, the patient's baseline immunosuppressive therapy was optimized with the addition of mycophenolic acid. No additional etiologies were identified to account for the new LV dysfunction. Following optimization of immunosuppressive therapy and heart failure management, the patient exhibited significant clinical improvement, including stabilization of cardiac function and resolution of inflammatory markers. This case report adds to sparse literature describing ATS-induced myocarditis and helps highlight integration of advanced imaging modalities like CMR, which provides critical insights into myocardial tissue characterization and helps guide management strategies.
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http://dx.doi.org/10.7759/cureus.80904 | DOI Listing |
Zhonghua Jie He He Hu Xi Za Zhi
September 2025
Department of Cardio-Pulmonary Circulation, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai 210032, China.
Antisynthetase syndrome(ASS) is an entity among the immune inflammatory myopathies(IIM), which always affects lungs. Interstitial lung disease(ILD) is common in ASS, while pulmonary hypertention(PH)is rarely observed. In this paper, we reported a case of ASS with ILD and PH.
View Article and Find Full Text PDFJ Med Virol
September 2025
Department of Pathology, West China Hospital, Sichuan University, Chengdu, China.
Systemic chronic active Epstein-Barr virus disease (sCAEBVD) can primarily involve skeletal muscle to form CAEBV-myopathy (CAEBV-M), which may resemble idiopathic inflammatory myopathies (IIMs). This study reports an 11-patient, 10-year cohort of CAEBV-M to summarize clinicoseropathologic features. CAEBV-M typically affects young adults (median: 29 years), with universal limb swelling, frequent disseminated muscle involvement (73%), and systemic symptoms like fever (82%), splenomegaly (82%), and hemophagocytic lymphohistiocytosis (55%).
View Article and Find Full Text PDFCancer Manag Res
August 2025
Department of Hematology, Beijing Longfu Hospital, Beijing, People's Republic of China.
Glofitamab, a CD20×CD3 T-cell-engaging bispecific monoclonal antibody, has emerged as a promising therapeutic agent for relapsed/refractory B-cell non-Hodgkin lymphoma. The advent of chimeric antigen receptor T-cell therapy and T-cell-engaging bispecific antibodies has also stimulated growing interest in their potential application in autoimmune diseases. Here, we report a case of diffuse large B-cell lymphoma (DLBCL) in a patient with a long-standing history of antisynthetase syndrome (ASyS).
View Article and Find Full Text PDFJ Cachexia Sarcopenia Muscle
October 2025
Department of Rheumatology and Immunology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Background: Idiopathic inflammatory myopathies (IIMs) exhibit diverse cellular microenvironments in muscle tissues, yet the full spectrum of cell populations and changes remains unclear. This study aimed to characterize cellular heterogeneity, explore cell-cell interactions and assess the prognostic value of cell subtype abundances across IIM subtypes in Han Chinese.
Methods: Muscle samples from six IIMs and three normal controls (NC) underwent single-cell RNA sequencing (scRNA-seq), whereas bulk RNA sequencing was performed on 203 IIMs and 19 NC.
Front Immunol
August 2025
Department of Rheumatology and Immunology, Beijing Shunyi Hospital, Beijing, China.
Objective: The coexistence of psoriatic arthritis (PsA) with inflammatory myopathies, including antisynthetase syndrome (ASS), is exceptionally rare and presents significant diagnostic and therapeutic challenges. This study reports a case of PsA overlapping with ASS and reviews the literature to analyze clinical features, immunopathogenesis, and treatment strategies.
Methods: A 52-year-old female with a 10-year history of psoriasis developed PsA and later presented with muscle weakness, mechanic's hands, and interstitial lung disease (ILD).