Primary Cardiac Sarcoma in Pregnancy: A Case Report

نویسندگان

  • Geum Joon Cho
  • Hai Joong Kim
  • Jae Seong Kang
چکیده

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.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Primary Synovial Sarcoma Presenting as a Huge Mass: A Report of a Rare Case and Review of Literature

Primary synovial sarcoma of mediastinum is very rare among soft tissue sarcomas. Only a few cases have been reportedin the literatures. The best treatment is still unclear, but, surgical resection is the main therapy. In this article we reporta case of a 20*20 cm (2000gr) primary giant mediastinal synovial sarcoma in a 42 year-old man. We performed radicalexcision of the tumor...

متن کامل

DIAGNOSIS OF PRIMARY CARDIAC TUMORS: REPORT OF 30 CASES

Between I 9H I and 1993,30 cases of primary cardiac tumors were diagnosed at the Imam Khomeini Hospital. 20 patients were female and 10 were male, with an average age of 32 years (ranging from 17 days to 65 years of age). The mean duration of symptoms before diagnosis was 6 months, with dyspnea and palpitation being the most common symptoms (60%) and cardiac' murmurs the most usual signs (...

متن کامل

A novel case of quartet tumor: meningioma, angiomyolipoma, ependymoma and sarcoma: report of a case and review of the literature

Multiple primary tumors in a single patient are relatively rare when four or more distinct lesions are considered. Herein, we report a case of woman with four different primary tumors: meningioma, renal angiomyolipoma, spinal ependymoma and high-grade soft tissue sarcoma. There was no family history and hereditary syndrome. The genetic analysis was completely normal. To best of our knowledge, t...

متن کامل

Cardiac angiosarcoma Report of a case

ABSTRACT Sarcomas are the most malignant tumors in the myocardium. Most common sarcoma is theangiosarcoma, classically located in the right atrium. Surgical resection is the primary treatmentof choice for these patients. In July 2003, an 18 years old man with chest pain and dyspnea,referred to the Imam Khomeini Hospital. Chest X-ray showed cardiac enlargement andtransthoracic echocardiography d...

متن کامل

Extraskeletal Ewing’s Sarcoma of Neck in a Child- A Case Report

Introduction: Ewing's sarcoma (ES) is an extremely rare bone malignancy observed in otorhinolaryngeal practice. In otorhinolaryngology, it sometimes involves the facial bones and cervical vertebrae. In children, ES is the second most common primary malignancy of bone after osteosarcoma. Extraskeletal Ewing’s sarcoma (EES) is an extremely rare malignancy of mesenchymal cell origin. The EES...

متن کامل

Primary Extraosseous Ewing Sarcoma of the Maxillary Sinus in an Adult-A Rare Case Report

Introduction: Ewing sarcoma (ES), which is described as diffuse endothelioma of the bone, is divided into osseous and extraosseous Ewing sarcoma (EES) mostly affecting children and adolescents. It is a rare, aggressive, and poorly differentiated small blue round cell tumor that seldom affects the head and neck regions.   Case Report: Herein, we reported a 46-year-old ma...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره 21  شماره 

صفحات  -

تاریخ انتشار 2006