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Cardiac osteosarcoma: a case report and literature review.
Bae, Dae-Hwan; Park, Sangshin; Kim, Min; Kim, Sangmin; Choi, Woong Gil; Bae, Jang-Whan; Hwang, Kyung-Kuk; Kim, Dong-Woon; Cho, Myeong-Chan; Lee, Ju-Hee.
Afiliação
  • Bae DH; Department of Cardiology, Chungbuk National University Hospital, Cheongju, Republic of Korea.
  • Park S; Department of Cardiology, Chungbuk National University Hospital, Cheongju, Republic of Korea.
  • Kim M; Department of Cardiology, Chungbuk National University Hospital, Cheongju, Republic of Korea.
  • Kim S; Department of Cardiology, Chungbuk National University Hospital, Cheongju, Republic of Korea.
  • Choi WG; Department of Cardiology, Chungbuk National University College of Medicine, Cheongju, Republic of Korea.
  • Bae JW; Department of Cardiology, Chungbuk National University Hospital, Cheongju, Republic of Korea.
  • Hwang KK; Department of Cardiology, Chungbuk National University College of Medicine, Cheongju, Republic of Korea.
  • Kim DW; Department of Cardiology, Chungbuk National University Hospital, Cheongju, Republic of Korea.
  • Cho MC; Department of Cardiology, Chungbuk National University College of Medicine, Cheongju, Republic of Korea.
  • Lee JH; Department of Cardiology, Chungbuk National University Hospital, Cheongju, Republic of Korea.
Front Cardiovasc Med ; 10: 1215389, 2023.
Article em En | MEDLINE | ID: mdl-37492160
ABSTRACT

Background:

Primary cardiac tumors are rare, and malignant primary cardiac tumors are even rarer. Cardiac osteosarcoma is a very rare type of malignant primary cardiac tumor with limited reported cases. We present a case report of cardiac osteosarcoma and review its characteristics and the related literature. Case

summary:

A 44-year-old female patient without a specific medical history presented with intermittent dyspnea that started 1 month prior to presentation. A heterogeneous mass was observed in the left atrium on echocardiography and a large mass was observed in the left atrium on computed tomography. Surgery was performed under the suspicion of atypical cardiac myxoma, and the tumor was successfully removed. However, postoperative histopathological examination revealed cardiac osteosarcoma. The patient underwent chemotherapy and has been well maintained without recurrence for 10 years.

Conclusion:

We present a case report of the echocardiographic features and treatment strategies for cardiac osteosarcoma, an extremely rare cardiac tumor. Multimodal imaging can be helpful; however, a histological diagnosis through surgical resection is essential. Appropriate treatment and follow-up based on histological findings are necessary.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article