The Coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory
syndrome coronavirus 2 has been rapidly spreading globally and has caused worldwide …

Cardiac tumours can occur in association with genetic syndromes. Rhabdomyomas have
been reported in association with tuberous sclerosis, myxomas with Carney's complex …

Introduction Cardiac angiosarcoma is a very rare disease. As a result of their nonspecific
presentation symptoms, and the lack of consensus in treatment, caution should be taken in …

Background Cardiac sarcomas are rare and aggressive tumors with little known about the
demographics, genetics, or treatment outcomes. Objectives The objectives of this study were …

Primary cardiac tumors are uncommon. Rhabdomyosarcomas are among the rarest type of
cardiac sarcomas. Echocardiography, cardiac MRI, and computed tomography scan can …

Background Primary intimal sarcomas of the heart are extremely rare and have a dismal
prognosis. Their management represents a complex clinical challenge since complete …

Sophisticated cancer treatments, cardiovascular risk factors, and aging trigger acute
cardiovascular diseases in an increasing number of cancer patients. Among acute …

Primary malignant cardiac tumors (PMCTs) are rare but lethal neoplasms. There are limited
evidence-based treatment guidelines for PMCTs. We evaluated the relation of …

Abstract “Cases of SCMR” is a case series on the SCMR website (https://www. scmr. org) for
the purpose of education. The cases reflect the clinical presentation, and the use of …

Cardiac angiosarcoma is the most common malignant tumor of the heart. The typical clinical
profile is a young male with 30–50 years of age. Due to varied clinical presentation, it can …