Case Report: Primary cardiac synovial sarcoma invading the tricuspid valve in a pregnant woman

Primary cardiac synovial sarcoma (PCSS) is a rare and highly aggressive tumor with a significant mortality rate. Treatment guidelines have not been defined given the relative rarity of the condition, especially for pregnant women. Described herein is a 36-year-old pregnant woman at 29 weeks with gestation who was hospitalized due to chest tightness and nausea, and echocardiography found a mass involved in the right heart and the tricuspid valve. She had to undergo cardiac surgery because the mass almost blocked the opening of the tricuspid valve. She underwent a radical resection of the masses and tricuspid valve, followed by replacement of the tricuspid valve with a mechanical valve. She successfully delivered a healthy baby boy. The diagnosis of synovial sarcoma is confirmed by positive results indicating rearrangement of the SYT gene. The patient survived throughout the 30-month follow-up period. There are no reported cases of pregnant women diagnosed with cardiac synovial sarcoma and have undergone cardiac surgery and cesarean section. Our treatment plan not only maximizes patient survival but also ensures fetal survival. This situation is rare and needs documentation.

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Publication Details

Journal
Frontiers in Cardiovascular Medicine
Published
2024-10-18
DOI
https://doi.org/10.3389/fcvm.2024.1437903
Citations
3
Primary Topic
Cardiac tumors and thrombi
Type
article
Field-Weighted Citation Impact
1.21
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article

Case Report: Primary cardiac synovial sarcoma invading the tricuspid valve in a pregnant woman

Maoxun Huang, Kexiang Liu, Man Li, Yong Wang et al.
3 citations
Frontiers in Cardiovascular Medicine
Cardiac tumors and thrombi
1.21
article

Case Report: Primary cardiac synovial sarcoma invading the tricuspid valve in a pregnant woman

Maoxun Huang, Kexiang Liu, Man Li, Yong Wang, Hulin Piao
article en
3 citations

Abstract

Primary cardiac synovial sarcoma (PCSS) is a rare and highly aggressive tumor with a significant mortality rate. Treatment guidelines have not been defined given the relative rarity of the condition, especially for pregnant women. Described herein is a 36-year-old pregnant woman at 29 weeks with gestation who was hospitalized due to chest tightness and nausea, and echocardiography found a mass involved in the right heart and the tricuspid valve. She had to undergo cardiac surgery because the mass almost blocked the opening of the tricuspid valve. She underwent a radical resection of the masses and tricuspid valve, followed by replacement of the tricuspid valve with a mechanical valve. She successfully delivered a healthy baby boy. The diagnosis of synovial sarcoma is confirmed by positive results indicating rearrangement of the SYT gene. The patient survived throughout the 30-month follow-up period. There are no reported cases of pregnant women diagnosed with cardiac synovial sarcoma and have undergone cardiac surgery and cesarean section. Our treatment plan not only maximizes patient survival but also ensures fetal survival. This situation is rare and needs documentation.

Frontiers in Cardiovascular MedicineVol. 11
Second Affiliated Hospital of Jilin University (CN)
Good health and well-being
Openalex Percentile: Top 18%
Cardiac tumors and thrombi
1.21
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