ReviewBMC cardiovascular disorders2020
Case report: left atrial Myxoma causing elevated C-reactive protein, fatigue and fever, with literature review.
Review in BMC cardiovascular disorders, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed, 18 citations in OpenAlex.
- Early surgical outcomes of cardiac myxoma resection according to dominant clinical phenotype in adult patients.Northern clinics of Istanbul · 2026Article
- Cardioembolic stroke secondary to a cardiac myxoma.Radiology case reports · 2025Article
- Article
- Cardiac myxoma: a comprehensive review.Journal of cardiothoracic surgery · 2025Review
- Infected left atrial myxoma withFrontiers in oncology · 2025Article
- Article
- Case Report: Atrial myxoma combined with hyperthyroidism in an adolescent with literature review.Frontiers in oncology · 2023Article
- Article
- A case report of left atrial myxoma presenting with amnesia.BMC cardiovascular disorders · 2021Article
- Autopsy of 54 cases of surgically excised cardiac myxomas. Investigation of their impact on immune response.Heliyon · 2020Article
- A Case of Dyspnea in a Patient with a Previous Coronavirus Disease Infection: Pulmonary is not always the Cause.Journal of cardiovascular echographyArticle
- The Importance of Ultrasound in a Case of Stroke Caused by Left Atrial Myxoma.Journal of cardiovascular echographyArticle
Corrections and comments
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundA cardiac myxoma in a young person may pose a diagnostic challenge as symptoms may be variable and the differential diagnosis is wide. The differential diagnosis can include rheumatic mitral valve disease, pulmonary hypertension, endocarditis, myocarditis and vasculitis. CASE PRESENTATION: This case report involves a 49 years old female with a 2.8 cm × 3.4 cm myxoma in the left atrium causing mitral valve obstruction. She presented with fatigue, fever of unknown origin, transient ischemic attack and shortness of breath. Prompt surgery is often recommended due to the risk of embolic complications or complete obstruction. Due to her symptoms, patient underwent successful cardiothoracic surgery to excise the myxoma within 2 weeks of confirmation by cardiac echocardiography.
conclusionThis case also emphasizes the diagnostic challenge as symptoms may be variable, ranging from fatigue, fever and shortness of breath to transient ischemic attack and at worst, sudden cardiac death. In conclusion, if a cardiac mass is suspected, echocardiography should be performed early. Surgical resection is curative and recurrence rate is very rare in sporadic isolated myxomas, however, recurrence can be higher in genetic diseases associated with increased frequency of myxomas such as Carney complex. This subpopulation of patients may present further research opportunity to learn more about the perioperative management of patients with myxomas such as determining the optimal time to surgical intervention and decision to anticoagulate.
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