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Primary cardiac sarcoma in pregnancy: a case report.
Geum Joon Cho1, Hai Joong Kim, Jae Seong Kang
1Department of Obstetrics and Gynecology, College of Medicine, Korea University, Seoul, Korea.
Journal of Korean Medical Science
|October 18, 2006
Summary
Primary cardiac sarcoma is rare and aggressive. Surgical removal during pregnancy is possible, enabling fetal development, but long-term survival remains poor for these rare cardiac tumors.
Area of Science:
- Cardiology
- Oncology
- Obstetrics
Background:
- Primary cardiac sarcoma is a rare malignancy with a poor prognosis in adults.
- The co-occurrence of cardiac sarcoma and pregnancy is exceptionally rare, posing unique clinical challenges.
Observation:
- A pregnant patient at 27 weeks gestation presented with acute dyspnea due to a left atrial mass.
- Transthoracic echocardiography confirmed the intracardiac mass.
Findings:
- Surgical resection of the cardiac sarcoma and valve repair were performed, followed by chemotherapy.
- The patient delivered a viable infant at 29 weeks gestation.
- Despite treatment, the patient died 10 months post-diagnosis.
Implications:
- Surgical intervention for cardiac tumors in pregnant patients is feasible and can facilitate prolonged gestation.
- While challenging, attempting tumor removal can improve fetal outcomes, despite poor maternal survival rates.
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