Key result
Multimodal therapy halts metastatic growth and shrinks lesions at 6 weeks in a cardiac sarcoma case.
Case Report (n=1)
This case highlights the aggressive nature of primary cardiac sarcoma and the necessity of multimodal, repeat surgical intervention for CNS involvement in a pediatric patient.
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May inform multimodal strategies for rare cardiac sarcoma CNS spread; extends case data but leaves open need for prospective validation.
An 18-year-old Hispanic male with an unremarkable medical history presented with a 1-month history of progressive, intermittent headaches, nausea, and diplopia. Upon seeking care, a head CT revealed a solid right frontal lesion and a large, complex cystic parieto-occipital lesion exerting significant mass effect on surrounding structures. The patient initially underwent a left parietal craniotomy for tumor resection, followed by resolution of his neurological symptoms. However, surveillance imaging 1 month later identified a known left atrial cardiac mass and new intracranial embolic infarcts, alongside a 6-cm recurrence at the primary resection site. The patient subsequently underwent a sternotomy for resection of the primary cardiac sarcoma and reconstruction of the left atrium. Shortly after, a second craniotomy was required for resection due to rapid cystic recurrence of the brain metastasis causing midline shift and new focal neurological deficits. Following successful gross-total re-resection, the patient underwent hypofractionated Gamma Knife radiosurgery. He is also undergoing chemotherapy. Six-week follow-up imaging confirmed a positive response to treatments, showing no new metastatic growth and a reduction in the size of existing lesions. This case highlights the aggressive nature of primary cardiac sarcoma and the necessity of multimodal, repeat surgical intervention for CNS involvement.
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Stoltzfus et al. (2026) conducted a case report in Primary cardiac sarcoma with intracranial metastasis and embolic infarction (n=1). Multimodal therapy (surgery, radiosurgery, chemotherapy) was evaluated on Clinical and radiographic response. Multimodal treatment including surgery, radiosurgery, and chemotherapy led to no new metastatic growth and reduced lesion size at 6-week follow-up in an 18-year-old with primary cardiac sarcoma.
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