ArticleBMC cardiovascular disorders2014
Biatrial myxoma and multiple organ infarctions combined with Leriche syndrome in a female patient.
Article in BMC cardiovascular disorders, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 12 citations in OpenAlex.
- Atrial Myxoma in Both Chambers: Biatrial or Bilateral? A Rare Case Resected via Endoscopic Approach and Literature Review.Medical sciences (Basel, Switzerland) · 2025Review
- Renal Embolism Associated with the Atrial Myxoma: A Case Report and Literature Review.Medicina (Kaunas, Lithuania) · 2024Review
- Acute Lower Limb Ischaemia as a Presenting Sign of Atrial Myxoma: Case Report and Scoping Review of the Literature.EJVES vascular forum · 2024Article
- Neurological Complications of Cardiac Tumors.Current neurology and neuroscience reports · 2019Review
- Article
- Outcomes of Patients with Newly Diagnosed Cardiac Myxoma: A Retrospective Multicentric Study.BioMed research international · 2018Article
- Biatrial myxoma floating like a butterfly: A case report and review of the literature.Medicine · 2018Review
- Leriche Syndrome Presenting as Depression with Erectile Dysfunction.Journal of clinical and diagnostic research : JCDR · 2016Article
Corrections and comments
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Authors and funding
6 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundMultiple organ infarctions combined with Leriche syndrome due to embolic particles of myxoma are very rare. There is no definite guideline for immediate medical treatment. CASE PRESENTATION: A 36-year-old married female was referred to the emergency department (ED) with severe pain of both lower extremities and gradual decreased mental status. Brain magnetic resonance imaging (MRI) and computed tomography angiography (CTA) revealed acute multiple organ infarctions including the brain, spleen, and bilateral kidneys combined with Leriche syndrome. To evaluate the embolic source, echocardiography was performed and it revealed biatrial myxoma. Because of the risk of progression in systemic embolic events, surgical excision and embolectomy were performed urgently. After the operation, renal function was recovered, and the pain of both limbs was relieved. However, the visual field defect due to the brain infarction remained. She was discharged uneventfully on the fourteenth postoperative day.
conclusionThis was an extremely rare case of multiple organ infarctions combined with Leriche syndrome as the initial presentation of biatrial myxoma. The treatment of choice for myxoma is surgical excision, but the optimal timing of operations is still controversial in patients who have had recent neurological insults. Echocardiography was useful to clarify the diagnosis and decide on the proper treatment modality: surgical treatment or thrombolysis.
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