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Pericardial malignant solitary fibrous tumour with right atrial invasion – a case report and literature review

机译:心包侵袭性心包恶性孤立性纤维瘤-一例报告并文献复习

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摘要

Solitary fibrous tumours are unusual neoplasms that develop from mesenchymal cells, usually originating from the pleura. A pericardial solitary fibrous tumour is an extremely rare occurrence. We report a 64-year-old woman who presented to the hospital with chief complaints of dyspnoea and abdominal distension. Echocardiography and enhanced computed tomography revealed an intrapericardial tumour with local invasion to the right atrium. Histopathological examination of a biopsy specimen showed a patternless distribution of spindle-shaped cells in a collagen stroma, with a high mitosis rate. Immunohistochemistry was positive for vimentin, CD34, and Bcl-2. The final diagnosis was a pericardial malignant solitary fibrous tumour with right atrial invasion. Surgical resection of the tumour was not performed because of its invasion into the myocardium. We systematically reviewed the literature on cardiac solitary fibrous tumours up to 2019.
机译:孤立性纤维性肿瘤是从间充质细胞发展而来的罕见肿瘤,通常起源于胸膜。心包孤立性纤维性肿瘤极少发生。我们报告了一名主治呼吸困难和腹胀的主诉医院的64岁女性。超声心动图和增强型计算机断层扫描显示出心包内肿瘤,并向​​右心房局部浸润。活检标本的组织病理学检查显示胶原基质中纺锤形细胞无模式分布,有丝分裂率高。波形蛋白,CD34和Bcl-2的免疫组织化学呈阳性。最终诊断为心包恶性孤立性纤维性肿瘤伴右房侵犯。由于其侵入心肌,因此未进行手术切除。我们系统地回顾了截至2019年有关心脏孤立性纤维瘤的文献。

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