Abstract

To date, there have been less than a 100 confirmed case reports of primary cardiac malignant fibrous histiocytomas, a rare form of sarcoma. In this report, we discuss the case of a 15-year-old girl who initially presented with a histiocytic cerebral sarcoma that was treated with aggressive resection and chemotherapy. Three years later, the same patient developed increasing shortness of breath and was found to have a high-grade pleomorphic undifferentiated cardiac sarcoma that likely represents the primary tumour from which the cerebral lesion metastasised. This represents an extremely unique case; in 2010, a research group in Germany claimed the very first description of a true cardiac sarcoma with brain metastasis [1]. However, even as far back as 1960, there were three case reports [2] and more extensive sarcoma studies recently have revealed further cases [3]. Nevertheless, there have probably been less than 10 cases in the literature up until this point.

Highlights

  • This report highlights the case of a young patient who presented with an extremely rare histiocytoma brain tumour that was treated with surgery and extensive chemotherapy

  • During follow–up, two years later, she was found to have a cardiac sarcoma that likely represented the primary tumour of which the original brain deposit was a metastasis

  • We will present the literature on histiocytomas and primary cardiac and cerebral sarcomas that are all rare and form conclusions to help assist everyday practice when faced with these tumours

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Summary

Case Report

Copyright: © the authors; licensee ecancermedicalscience. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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