Primary intracranial sarcoma, DICER-1 mutant, with hemorrhagic presentation: A case report

B. Edelbach, Vadim Gospodarev, Ravi Raghavan, Justin Dye
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Abstract

Primary intracranial sarcomas (PIS) are rare tumors with mesenchymal origins. These tumors have a heterogeneous clinical presentation and are associated with a poor prognosis. This report highlights the complexities associated with PIS by focusing on a 26-year-old male with recurrent tumor growth facing unique challenges regarding diagnosis and treatment options . A high-grade spindle-celled neoplasm with sarcomatous features characterized the patient’s tumor. There were additional morphologic changes, including multinucleated giant cells and rare foci with eosinophilic spheroids. Genomic analysis revealed a DICER1-associated PIS. Treatment involved endovascular embolization, multiple surgical interventions, intrathecal etoposide injections, and oral pazopanib with adjuvant radiation therapy. This case additionally highlights an unusual association between PIS and anomalous hypervascularity, refractory hemorrhage, and subdural effusions, a presentation that is increasingly being reported in this type of tumor.
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原发性颅内肉瘤,DICER-1 突变,伴出血性表现:病例报告
原发性颅内肉瘤(PIS)是一种罕见的间叶源性肿瘤。本报告以一名 26 岁的男性为例,重点介绍了与原发性颅内肉瘤相关的复杂性,他的肿瘤反复生长,在诊断和治疗方案方面面临着独特的挑战。患者的肿瘤为高级别纺锤形细胞肿瘤,具有肉瘤特征。肿瘤还出现了其他形态学变化,包括多核巨细胞和罕见的嗜酸性球形病灶。基因组分析显示,这是一种与 DICER1 相关的 PIS。治疗包括血管内栓塞、多次手术干预、鞘内注射依托泊苷、口服帕唑帕尼并辅助放疗。该病例还强调了PIS与异常高血管性、难治性出血和硬膜下积液之间不寻常的关联,这种表现在此类肿瘤中的报道越来越多。
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