Cardiac Angiosarcoma in the Right Atrium Treated by Surgical Resection
Milica Dragicevic-Antonic1, Ljiljana Rankovic-Nicic1,2, Gordana Stamenkovic1
1Institute for Cardiovascular Diseases "Dedinje", 11000 Belgrade, Serbia.
Medicina (Kaunas, Lithuania)
|August 29, 2024
Summary
This case study details a rare intracardiac angiosarcoma in a 49-year-old female. Early surgical intervention and vigilant monitoring are crucial for managing this aggressive cardiac tumor.
Area of Science:
- Cardiology
- Oncology
- Pathology
Background:
- Primary intracardiac angiosarcoma is a rare and aggressive malignancy.
- Early diagnosis and intervention are critical for patient outcomes.
Observation:
- A 49-year-old female presented with chest tightness, fatigue, and palpitations.
- Echocardiography revealed a right atrial mass, confirmed as high-grade angiosarcoma post-surgery.
- Recurrence with superimposed thrombus and Takotsubo cardiomyopathy were noted postoperatively.
Findings:
- Surgical excision and adjuvant chemotherapy with Paclitaxel were administered.
- Anticoagulation with Warfarin was initiated due to recurrent thrombus and cardiomyopathy.
- Cardiac MRI confirmed recurrent angiosarcoma with thrombus.
Implications:
- This case underscores the challenges in diagnosing and treating intracardiac angiosarcoma.
- Advanced imaging and meticulous postoperative surveillance are essential.
- Multidisciplinary management is key for optimizing care in complex cardiac tumor cases.
Keywords:
Takotsubo cardiomyopathyangiosarcomacardiac magnetic resonance imagingmultidisciplinary approachMore Related Videos
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