Recurrent pheochromocytoma with catecholamine cardiomyopathy and left ventricular thrombus: a case report.
Renzheng ChenYong WangJie YangXiaofeng ChengJiang WangLan HuangPublished in: The Journal of international medical research (2021)
Pheochromocytoma is a rare and usually benign tumor of the adrenal glands. We report a case of a 40-year-old woman with recurrent pheochromocytoma and catecholamine cardiomyopathy. She had no history of other types of tumors or connective tissue disease. She had already undergone surgery twice to remove the pheochromocytoma, which had now recurred for the second time. A thrombus in the left ventricle was also noted upon imaging examination, which dissipated after anticoagulation therapy using dabigatran, allowing the patient to opt for an elective third surgery. This paper describes the clinical outcome of using the anticoagulant dabigatran to treat left ventricular thrombosis in this rare case of recurrent pheochromocytoma, and thus further contributing to the knowledge of the clinical management of this rare and complicated disease.
Keyphrases
- atrial fibrillation
- left ventricular
- heart failure
- rare case
- minimally invasive
- coronary artery bypass
- mitral valve
- venous thromboembolism
- healthcare
- high resolution
- acute myocardial infarction
- left atrial
- hypertrophic cardiomyopathy
- cardiac resynchronization therapy
- patients undergoing
- surgical site infection
- percutaneous coronary intervention
- pulmonary hypertension
- aortic stenosis
- photodynamic therapy
- acute coronary syndrome
- coronary artery disease
- mesenchymal stem cells
- congenital heart disease
- catheter ablation
- bone marrow
- replacement therapy