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A case report of a massive cardiac intimal sarcoma manifesting as syncope during a stress test

BACKGROUND: Syncope has many aetiologies but from a cardiac standpoint, if arrhythmogenic and ischaemic causes are not present, obstructive lesions should be considered. Cardiac spindle cell sarcomas are incredibly rare and difficult to cure. CASE SUMMARY: A 62-year-old man presented for exercise st...

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Detalles Bibliográficos
Autores principales: Rehman, Mahin, El-Dabh, Ashraf, Mandal, Shobha, Sattur, Sudhakar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343455/
https://www.ncbi.nlm.nih.gov/pubmed/34377908
http://dx.doi.org/10.1093/ehjcr/ytab258
Descripción
Sumario:BACKGROUND: Syncope has many aetiologies but from a cardiac standpoint, if arrhythmogenic and ischaemic causes are not present, obstructive lesions should be considered. Cardiac spindle cell sarcomas are incredibly rare and difficult to cure. CASE SUMMARY: A 62-year-old man presented for exercise stress test and had a syncopal episode on the treadmill. He was found to have a massive mass obstructing the transmitral flow. Patient was taken to the operating room and the mass was resected successfully. Histopathological confirmation revealed the mass to be a cardiac intimal sarcoma. Patient was initiated on a trial regimen of doxorubin, ifosfamide, and mesna. DISCUSSION: Cardiac intimal sarcomas are aggressive cancers and are difficult to treat; there are no established treatment guidelines. They can lead to obstruction of blood flow through the cardiac chambers. From a cardiac perspective, without arrhythmogenic and ischaemic causes of syncope, obstructive lesions should be considered.