关键词: Dural based Grade Hemangiopericytoma Intracranial Solitary fibrous tumor

Mesh : Humans Solitary Fibrous Tumors / pathology Adult Male Female Middle Aged Brain Neoplasms / pathology diagnostic imaging Retrospective Studies Young Adult STAT6 Transcription Factor / analysis genetics Biomarkers, Tumor / analysis Immunohistochemistry Adolescent Diagnosis, Differential Meningioma / pathology diagnostic imaging diagnosis

来  源:   DOI:10.1016/j.prp.2024.155456

Abstract:
BACKGROUND: Intracranial solitary fibrous tumors (SFTs) are rare mesenchymal neoplasms, often challenging to diagnose due to their resemblance to meningiomas and other central nervous system tumors. While advancements in molecular genetics have aided in classification, diagnostic nuances and optimal management strategies remain areas of interest.
METHODS: This retrospective study analyzed 11 cases of intracranial SFTs treated at a neurosurgical centre in India between February 2020 and January 2024. Clinical data, radiological findings, histopathological features, and follow-up details were reviewed. Immunohistochemistry, particularly STAT6, facilitated diagnosis confirmation.
RESULTS: The median age of presentation was 32 years, with a male predominance. Headache was the most common presenting symptom, often leading to misdiagnosis as meningiomas on radiological imaging. Histologically, SFTs exhibited spindle to ovoid cells with staghorn vessels and collagenized stroma, posing challenges in differential diagnosis. WHO grading predominantly revealed grade 1 tumors, though recurrence occurred, emphasizing the importance of long-term follow-up. Immunohistochemistry, particularly STAT6, played a pivotal role in distinguishing SFTs from other entities.
CONCLUSIONS: Intracranial SFTs present diagnostic challenges due to overlapping features with other tumors, warranting a comprehensive approach integrating clinical, radiological, and histopathological findings. Immunohistochemistry, particularly STAT6, emerges as a valuable diagnostic tool. Long-term follow-up is essential for monitoring recurrence and potential malignant transformation. Further research is needed to delineate optimal treatment strategies, including the role of radiotherapy in SFT management.
摘要:
背景:颅内孤立性纤维性肿瘤(SFT)是罕见的间充质肿瘤,由于它们与脑膜瘤和其他中枢神经系统肿瘤相似,通常难以诊断。虽然分子遗传学的进步有助于分类,诊断细微差别和优化管理策略仍然是人们感兴趣的领域。
方法:这项回顾性研究分析了2020年2月至2024年1月在印度神经外科中心治疗的11例颅内SFT。临床数据,放射学发现,组织病理学特征,和随访细节进行了审查。免疫组织化学,特别是STAT6,促进诊断确认。
结果:就诊年龄中位数为32岁,男性占主导地位。头痛是最常见的症状,常导致影像学误诊为脑膜瘤。组织学上,SFT表现为梭形至卵形细胞,鹿角状血管和胶原基质,在鉴别诊断中提出了挑战。WHO分级主要显示1级肿瘤,虽然复发,强调长期跟进的重要性。免疫组织化学,特别是STAT6,在区分SFT与其他实体方面发挥了关键作用。
结论:颅内SFT由于与其他肿瘤的重叠特征而存在诊断挑战,保证一个综合的方法,整合临床,放射学,和组织病理学发现。免疫组织化学,特别是STAT6,成为一种有价值的诊断工具。长期随访对于监测复发和潜在的恶性转化至关重要。需要进一步的研究来描述最佳的治疗策略,包括放疗在SFT管理中的作用。
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