Incidental High-Grade Sellar Solitary Fibrous Tumor Mimicking Non-Functioning Pituitary Adenoma: A Case Report and Literature Review.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Michele Persico, Brent D Weinberg, Stewart G Neill, Hui-Kuo Shu, Jim Zhong
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引用次数: 0

Abstract

BACKGROUND Sellar solitary fibrous tumors (SFT) are uncommon brain tumors belonging to the fibroblastic and myofibroblastic category of the 2021 World Health Organization (WHO) Classification of Central Nervous System (CNS) Tumors. Twenty-two instances of sellar WHO grade II and III SFT (SFT II/III) have been reported since 1983. SFTs II/III clinical and imaging findings resemble non-functioning pituitary adenomas (NFPAs). We report a 62-year-old woman with encephalopathy and an incidental WHO grade III sellar SFT presenting as a non-functioning pituitary mass. CASE REPORT A 62-year-old woman with encephalopathy and urosepsis was transferred for evaluation of an incidentally detected sellar mass. An endocrine workup was unremarkable and a presumed diagnosis of NFPA was made. A partial adenectomy was then performed through a trans-nasal trans-sphenoidal approach. Pathological analysis revealed a mesenchymal neoplasm with haphazardly arranged spindled to epithelioid cells, collagenized background, tortuous vasculature, high mitotic index, and Signal Transducer and Activator of Transcription 6 (STAT6) positivity. According to the 2016 CNS WHO guidelines, the diagnosis was an anaplastic hemangiopericytoma WHO grade III, now termed an SFT under the 2021 CNS WHO guidelines. Proton therapy to the dose of 59.4 gray given in 33 fractions was implemented adjuvantly. The residual tumor demonstrated shrinkage 1.5 years after proton therapy, and absence of recurrent disease after 3 years. CONCLUSIONS Sellar SFTs II/III can present as incidentalomas and be considered in the differential diagnosis of sellar masses. While some cause symptoms by local expansion mimicking NFPA presentations, local invasion and metastasis are reported. Surgical excision and pathologic confirmation guide management.

模仿无功能垂体腺瘤的偶发高级别ellar孤立性纤维瘤:病例报告和文献综述。
鞍区孤立性纤维性肿瘤(SFT)是2021年世界卫生组织(WHO)中枢神经系统(CNS)肿瘤分类中属于成纤维细胞和肌成纤维细胞类别的罕见脑肿瘤。自1983年以来已报告了22例世卫组织II级和III级SFT (SFT II/III)病例。SFTs II/III的临床和影像学表现类似于无功能垂体腺瘤(nfpa)。我们报告一个62岁的女性脑病和偶发的世卫组织III级鞍区SFT表现为无功能的垂体肿块。病例报告一名患有脑病和尿脓毒症的62岁妇女被转移以评估偶然发现的鞍块。内分泌检查无明显异常,推测诊断为NFPA。然后经鼻蝶入路行部分腺切除术。病理分析显示为间质肿瘤,梭形上皮样细胞杂乱排列,胶原背景,血管弯曲,有丝分裂指数高,转录信号传导和激活因子6 (STAT6)阳性。根据2016年CNS WHO指南,诊断为WHO III级间变性血管外皮细胞瘤,现在根据2021年CNS WHO指南称为SFT。质子治疗的剂量为59.4灰色,分33份给予辅助。残余肿瘤在质子治疗后1.5年缩小,3年后无复发。结论鞍区SFTs II/III可作为偶发瘤出现,可作为鞍区肿块的鉴别诊断依据。虽然一些引起症状的局部扩张模仿NFPA表现,局部侵袭和转移的报道。手术切除和病理确认指导治疗。
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来源期刊
American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
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