Shomal Zadeh Firoozeh, Azhideh Arash, Mantilla Jose G, Kosaraju Vijaya, Venugopal Nitin, Gaskin Cree M, Pooyan Atefe, Alipour Ehsan, Chalian Majid
Division of Musculoskeletal Imaging and Intervention, Department of Radiology, University of Washington, Seattle, WA 98915, USA.
Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA 98915, USA.
Diagnostics (Basel). 2023 May 2;13(9):1610. doi: 10.3390/diagnostics13091610.
To characterize the imaging features of patients with pathologically confirmed intraosseous schwannoma (IOS), institutional pathology and imaging databases were searched for IOS cases over a period of 17 years. A musculoskeletal radiologist evaluated all imaging studies. Additionally, a literature search was performed to identify IOS cases that had imaging findings of at least two modalities. Six patients (one female, five males, mean age of 50 ± 14 years) with IOS were identified, with all lesions localized to the lumbosacral region. Radiographic imaging was available in four patients, while all patients underwent CT and MR imaging. Radiographs depicted lytic lesions, and CT depicted heterogeneous expansile lesions with centrally hypodense areas and peripheral sclerosis. All cases involved extra-osseous extension, producing a mass effect on adjacent soft tissues and nerve roots. On MRI, the neoplasms displayed iso- to- slightly- low signal intensity on T1-weighted images and hyperintense signal intensity on T2-weighted images with heterogeneous enhancement. The literature review resulted in 102 IOS cases, which to the best of our knowledge, is the largest review on IOS, and the imaging findings of the previously published cases were the same as our cases. IOSs are rare benign neoplasms that should be considered in the differential diagnosis of well-defined expansile lytic lesions with sclerotic borders. This is particularly important in middle-aged adults with mandibular, sacral, or vertebral body mass.
为了描述经病理证实的骨内施万细胞瘤(IOS)患者的影像学特征,我们在机构病理和影像学数据库中搜索了17年间的IOS病例。一位肌肉骨骼放射科医生评估了所有影像学检查。此外,还进行了文献检索,以确定具有至少两种影像学检查结果的IOS病例。共识别出6例IOS患者(1例女性,5例男性,平均年龄50±14岁),所有病变均位于腰骶部。4例患者有X线片影像资料,所有患者均接受了CT和MR成像检查。X线片显示溶骨性病变,CT显示不均匀的膨胀性病变,中央低密度区和周边硬化。所有病例均累及骨外扩展,对相邻软组织和神经根产生占位效应。在MRI上,肿瘤在T1加权图像上呈等信号至略低信号强度,在T2加权图像上呈高信号强度,增强不均匀。文献综述共纳入102例IOS病例,据我们所知,这是关于IOS的最大规模综述,且既往发表病例的影像学表现与我们的病例相同。IOS是罕见的良性肿瘤,在鉴别诊断具有硬化边界的明确膨胀性溶骨性病变时应予以考虑。这在患有下颌骨、骶骨或椎体肿物的中年成年人中尤为重要。