Results 61 to 70 of about 689,585 (210)
Clinical Case Reports, Volume 14, Issue 7, July 2026.ABSTRACT Dedifferentiated liposarcoma (DDLPS) is a rare and aggressive subtype of soft tissue sarcoma, most commonly arising in the extremities or retroperitoneum. Cardiac involvement, whether primary or metastatic, is exceedingly rare and presents significant diagnostic and therapeutic challenges.
Azin Alizadehasl +2 more
wiley +1 more source
SURGICAL EXPERIENCE WITH INTRACARDIAC MYXOMAS [PDF]
Acta Medica Iranica, 2007 Cardiac myxoma is generally considered to be a surgical emergency. Surgical excision must be done as soon as possible after diagnosis because of the high risk of valve obstruction or systemic embolization.
N. Safaei +1 more
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Catastrophic antiphospholipid syndrome (CAPS) is a fulminant and rare variant of antiphospholipid syndrome characterized by rapidly progressive multiorgan thrombosis and a high mortality rate. Its diagnosis is often challenging due to overlapping clinical features with sepsis, thromboembolic disorders, and systemic autoimmune diseases.
Nazmin Ahmed +4 more
wiley +1 more source
Indian Journal of Pathology and Microbiology, 2017 Back ground: Glandular cardiac myxoma has varying clinical presentation with uncertain histogenesis and debatable immunohistochemical profile. Glandular epithelial differentiations are rare phenomenon known to be present as an intrinsic component of the ...
Devajit Nath +5 more
doaj +1 more source
Сardiac myxoma: challenge in diagnostics. Case report
Терапевтический архив, 2021 Cardiac myxoma is the most common primary benign cardiac tumor (up to 50% of all primary cardiac neoplasms). The implementation of the modern imaging techniques into the clinical practice, particularly, 2D echocardiography, computed tomography and ...
Victor V. Fomin +10 more
doaj +1 more source
Current Topics of Progressive Cardiac Conduction Disease
Journal of Arrhythmia, Volume 42, Issue 3, June 2026.Many genes and the protein cause PCCD. Mutation of NaV1.5 or CX40 cause isolated PCCD, but mutation of lamin A/C, emerin, or desmin lead to cardiomyopathy, and PCCD. Mutation of transcription factor NCX2‐5, and Tbx5 associated with atrial septal defect and abnormal development of conduction system.
Naokata Sumitomo +7 more
wiley +1 more source
Multiple arterial embolization from left atrial myxoma in a Maltese boy [PDF]
, 1994 Atrial myxoma is rare in adults and even rarer in children. In this article the author describes. The presentation may be with embolic, obstructive or constitutional symptoms, which may be dramatic and life-threatening.
Elliott, Martin, Vassallo Agius, Paul
core
Myxomatous cause of multiple intracranial aneurysms and cognitive decline: a case report
The Egyptian Heart JournalBackground The occurrence of cerebral aneurysm in a case of cardiac myxoma is rare with less than 60 cases reported worldwide. The course of management is still debatable given its rarity. We present a case of multiple intracranial aneurysms secondary to
Sudipta Mondal +4 more
doaj +1 more source
Cardiac myxoma with cartilaginous differentiation-An uncommon variant presented as mitral stenosis
Indian Journal of Pathology and Microbiology, 2019 The estimated incidence of primary cardiac tumors is extremely rare. Among it, cardiac myxoma represents the most common benign cardiac tumor constituting about 80% of cases. We are presenting a 30–year-old female with large left atrial myxoma.
Sunil V Jagtap +5 more
doaj +1 more source