Department of Radiology, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Medicine (Baltimore). 2022 Oct 21;101(42):e31355. doi: 10.1097/MD.0000000000031355.
Solitary fibrous tumor (SFT) is a rare mesenchymal spindle cell tumor. SFT in the central nervous system (CNS) is rare. This case reports rare magnetic resonance imaging (MRI) findings of intracranial SFT (ISFT).
We report a 47-year-old female patient who was found to have weakness in her right limb with walking instability 2 months before the visit.
Based on imaging, the provisional diagnosis was meningioma. Postsurgical histopathological diagnosis confirmed World Health Organization (WHO) grade I SFT/hemangiopericytoma (HPC).
The lesion was totally excised. The patient improved remarkably after the operation, without any signs of associated limb movement disorder.
No local recurrence or metastases were observed in the follow-up 3 months after the surgery.
Intracranial SFT is a rare mesenchymal tumor. Due to different tumor components, imaging manifestations are diverse and lack of characteristics, so preoperative diagnosis is challenging. Our case provides a rare ISFT with significantly decreased signal intensity in T2 weighted images (T2WI), which is an important supplement to the rare imaging findings of intracranial SFT.
孤立性纤维瘤(SFT)是一种罕见的间叶性梭形细胞肿瘤。中枢神经系统(CNS)中的 SFT 较为罕见。本病例报告了颅内 SFT(ISFT)罕见的磁共振成像(MRI)表现。
我们报告了 1 例 47 岁女性患者,其在就诊前 2 个月出现右侧肢体无力伴行走不稳。
根据影像学表现,初步诊断为脑膜瘤。术后组织病理学诊断证实为世界卫生组织(WHO)I 级 SFT/血管外皮细胞瘤(HPC)。
病变完全切除。术后患者显著改善,无肢体运动障碍相关迹象。
术后 3 个月随访未见局部复发或转移。
颅内 SFT 是一种罕见的间叶性肿瘤。由于不同的肿瘤成分,影像学表现多样且缺乏特征,因此术前诊断具有挑战性。我们的病例提供了一个罕见的 ISFT,其在 T2 加权图像(T2WI)上信号强度显著降低,这是对颅内 SFT 罕见影像学表现的重要补充。