Takotsubo cardiomyopathy in myasthenia gravis: a systematic review of case reports with subtype-based analysis
Hideya Itagaki, Takuro Hagino, Tomoyuki Endo

TL;DR
This paper reviews cases of Takotsubo cardiomyopathy in myasthenia gravis patients, highlighting its severity and clinical features.
Contribution
The study provides a systematic review and subtype-based analysis of a rare condition in MG patients.
Findings
Apical TTC was the most common subtype, occurring in 71.8% of cases.
Myasthenic crisis was the most frequent TTC trigger, reported in 37.5% of cases.
High mortality (17.5%) and ICU admission rates (97.4%) were observed in these patients.
Abstract
Takotsubo cardiomyopathy (TTC) is a stress-induced cardiac disorder characterized by transient left ventricular dysfunction. Myasthenia gravis (MG), an autoimmune neuromuscular disease, can precipitate TTC during exacerbations such as myasthenic crises. However, the clinical features and outcomes of TTC associated with MG remain unclear. We conducted a systematic review by the PRISMA guidelines. A comprehensive search of PubMed, Web of Science, and Google Scholar was performed up to May 31, 2025, using terms related to TTC and MG. Case reports and series were included if they described patients with confirmed diagnoses of both MG and TTC, with MG exacerbation occurring at the time of TTC onset. Data were extracted and compared between apical and non-apical TTC subtypes. Statistical analyses included the Mann-Whitney U test and chi-squared or Fisher’s exact test, as appropriate. A…
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Taxonomy
TopicsTakotsubo Cardiomyopathy and Associated Phenomena · Pericarditis and Cardiac Tamponade · Myasthenia Gravis and Thymoma
