医学
粘液瘤
恶性肿瘤
平滑肌肉瘤
肉瘤
内科学
左心房粘液瘤
病理
心脏病学
放射科
心房颤动
左心房
作者
Lucy Grant,I Morgan,Sumathi Vaiyapuri,Nabeel Salmons
标识
DOI:10.1016/j.jccase.2019.10.006
摘要
A 31-year-old female with a history of polycystic ovary syndrome and two recent miscarriages presented with symptoms of a transient ischemic attack. Echocardiography to assess for possible embolic source identified a 4.8 cm left atrial mass, presumed to be an atrial myxoma.At surgery the tumor was suspicious of malignancy. Histopathology revealed a heterogeneous hyper- and hypo-cellular spindle cell tumor showing mild atypia. Atrial myxoma markers were negative. The Ki67 proliferation factor was 30% and fluorescence in situ hybridization (FISH) analysis showed MDM2 amplification. Expert review confirmed the morphological, immunohistochemical, and FISH features to be of a cardiac intimal sarcoma.Recent improvements in imaging, surgery, and molecular testing have increased diagnoses of primary cardiac intimal sarcomas. Here we discuss the pathological and clinical implications of these rare atrial myxoma mimics.
科研通智能强力驱动
Strongly Powered by AbleSci AI