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DOI 10.3346/jkms.2006.21.5.940

Медицинская библиотека · Journal of Korean medical science · 2006

Primary cardiac sarcoma in pregnancy: a case report.

Cho Geum Joon, Kim Hai Joong, Kang Jae Seong

Клинический случайСтатьяПеревод пока не подготовлен

Аннотация

Primary cardiac sarcoma is a rare disease in adults. It is also associated with poor prognoses, due to diagnostic delay, therapeutic difficulty, and high metastatic potential. The coincidence of pregnancy and a primary cardiac intimal sarcoma is extremely rare. We report a pregnant woman at 27(+5) weeks gestation who was admitted to the hospital with acute-onset dyspnea. A mass was found on the left atrium by transthoracic echocardiography. Subsequently, the intracardiac mass was removed, and mitral valve replacement and modified DeVega tricuspid annuloplasty were performed. The patient was diagnosed with a undifferentiated sarcoma, and gave birth to a 1,230 g living baby boy by Caesarean section from preterm contraction at 29(+5) weeks gestation. The patient then received systemic chemotherapy. However, 10 months after the initial clinical onset, the patient suddenly died. Surgery is the standard treatment for cardiac tumors, and their removal should always be attempted, even in pregnant women. Although the overall survival rates of the patients are rather poor, palliative cardiac surgery allows the prolonging of pregnancy, until an acceptable fetal viability level is reached.

Для цитирования: Cho Geum Joon, Kim Hai Joong, Kang Jae Seong. Primary cardiac sarcoma in pregnancy: a case report.. Journal of Korean medical science. 2006. DOI: 10.3346/jkms.2006.21.5.940.

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Обработка статьи · этапы, ошибки и управление
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