2023, Number 4
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Cir Card Mex 2023; 8 (4)
Embryonal rhabdomyosarcoma of cardiac origin: case report
Echeverry-Gutiérrez MA, Martínez-Pérez AM, Cuevas-Álvarez R, Morales-Covarrubias CF, Castellanos-Gómez MO, Álvarez-Moreno CC
Language: English
References: 27
Page: 120-124
PDF size: 384.93 Kb.
ABSTRACT
Rhabdomyosarcoma is considered a mesenchymal neoplasm.
Due to its infrequency, there is no precise and protocolized
treatment standard at national and worldwide level. We present
the case of a young patient with symptoms of progressive
deterioration of functional class, dyspnea associated with
physical activity, orthopnea and paroxysmal nocturnal dyspnea,
is protocolized by suspicion of myxoma versus intracardiac
thrombus by echocardiography. Subsequently, it was
diagnosed as embryonal rhabdomyosarcoma with histological
studies obtained after tumor excision.
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