The Journal of Critical Care Medicine (Apr 2018)

Incidental Finding of a Left Atrial Myxoma while Characterising an Autoimmune Disease

  • Garcia-Carretero Rafael,
  • Naranjo-Mansilla Gema,
  • Luna-Heredia Esther,
  • Arias-Baldo Paloma,
  • Beamonte-Vela Blanca-Nieves

DOI
https://doi.org/10.2478/jccm-2018-0009
Journal volume & issue
Vol. 4, no. 2
pp. 64 – 67

Abstract

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Although cardiac tumours are uncommon, cardiac myxomas account for more than fifty percent of all cases and are the most frequent primary cardiac tumour. They have a broad clinical spectrum, usually related to cardiac symptoms, peripheral embolic events or systemic manifestations. We present a case report of a 68-year-old man who presented with systemic symptoms and analytical features suggestive of an autoimmune disease. In the ensuing diagnostic procedures, a cardiac myxoma was found, and after surgical resection, both the systemic manifestations and the analytical abnormalities disappeared.

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