Case series of rare primary cardiac sarcomas: A challenging histopathological diagnosis

Authors

  • Nguyen Van Hung Department of Pathology, Phenikaa University, Vietnam. Nguyen Trac Street, Ha Dong District, Hanoi, Viet Nam
  • Trinh Hoai Nam Department of Pathology, E Hospital. 89 Tran Cung Street, Cau Giay District, Hanoi, Viet Nam
  • Nguyen Cong Huu Cardiovascular Centre, E Hospital. 89 Tran Cung Steet, Cau Giay District, Hanoi, Viet Nam
  • Nguyen Tuan Thanh Pathological and cytopathological Centre, Bach Mai Hospital. 78, Giai Phong Street, Dong Da District, Hanoi, Viet Nam
  • Tran Ngoc Minh Pathological and cytopathological Centre, Bach Mai Hospital. 78, Giai Phong Street, Dong Da District, Hanoi, Viet Nam; Department of Pathology, Hanoi Medical University, Vietnam. 1, Ton That Tung Street, Dong Da District, Hanoi, Viet Nam
  • Nguyen Thi Nga Department of Pathology, E Hospital. 89 Tran Cung Street, Cau Giay District, Hanoi, Viet Nam
  • Nguyen Hoang Nam Cardiovascular Centre, E Hospital. 89 Tran Cung Steet, Cau Giay District, Hanoi, Viet Nam
  • Tran Van Chuong Pathological and cytopathological Centre, Bach Mai Hospital. 78, Giai Phong Street, Dong Da District, Hanoi, Viet Nam
  • Doan Minh Khuy Pathological and cytopathological Centre, Bach Mai Hospital. 78, Giai Phong Street, Dong Da District, Hanoi, Viet Nam
  • Dao Thi Luan Department of Pathology, Hanoi Medical University, Vietnam. 1, Ton That Tung Street, Dong Da District, Hanoi, Viet Nam; Department of Pathology, Hospital of Hanoi Medical University, Vietnam. 1, Ton That Tung Street, Dong Da District, Hanoi, Viet Nam
  • Hoang Thi Ngoc Mai Department of Pathology, Hospital of Hanoi Medical University, Vietnam. 1, Ton That Tung Street, Dong Da District, Hanoi, Viet Nam

DOI:

https://doi.org/10.15419/bmrat.v10i2.791

Keywords:

cardiac angiosarcoma, cardiac leiomyosarcoma, cardiac lymphoma, cardiac rhabdomyosarcoma, rare primary cardiac sarcomas

Abstract

Primary cardiac sarcomas are rare and histologically diverse, with single tumors able to demonstrate histological heterogeneity. Consequently, they are often misdiagnosed as other common cardiac tumors, such as cardiac myxoma or other metastatic malignancies. Incorrect diagnoses can result in incomplete surgeries, inadequate treatment regimens, and early recurrence. In our experience, based on the diverse histological and cytological characteristics of these tumors, immunostaining panels should be used early on to differentiate the exact tumor type. SMA, CD31, myogenin, ERG, and SOX10 panels are used to identify spindle-shaped or polymorphic cell patterns, while CK, LCA, S100, and desmin panels are used for round and monomorphic cell patterns. Using these panels can help identify the histological type of primary cardiac sarcomas, which is normally a challenge for pathologists.

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Published

2023-02-28

Issue

Section

Case report

How to Cite

Case series of rare primary cardiac sarcomas: A challenging histopathological diagnosis. (2023). Biomedical Research and Therapy, 10(2), 5530-5536. https://doi.org/10.15419/bmrat.v10i2.791

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