Rapidly progressive malignant fibrous histiocytoma of right atrium: A rare case report

2Citations
Citations of this article
17Readers
Mendeley users who have this article in their library.
Get full text

Abstract

We are going to present a case of malignant fibrous histiocytoma in the right atrium, which is a very rare entity. The patient had a right atrial mass, which prolapsed through the tricuspid valve into the right ventricle, causing functional tricuspid valve stenosis. The tumor was completely resected and the patient had an uneventful postoperative period. Histopathological examination reported malignant fibrous histiocytoma. The patient presented to the emergency department five weeks after discharge with dyspnea and palpitation. Echocardiography and magnetic resonance imaging revealed recurrent right atrial tumor mass. His clinical status has worsened, with syncope and acute renal failure. On the repeated echocardiography, suspected tumor recurrence was observed in left atrium, which probably caused systemic embolization. Considering the aggressive nature of the tumor and systemic involvement, our Heart Council decided to provide palliative treatment by nonsurgical management. His status deteriorated for the next few days and the patient succumbed to a cardiac arrest on the 4th day.

Cite

CITATION STYLE

APA

Aksu, T., Gode, S., Oz, K., Ersoy, B., Tel Ustunısık, C., Guner, Y., … Erentug, V. (2019). Rapidly progressive malignant fibrous histiocytoma of right atrium: A rare case report. Brazilian Journal of Cardiovascular Surgery, 34(3), 372–376. https://doi.org/10.21470/1678-9741-2018-0114

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free