Department of Radiology, Mayo Clinic, Charlton Building North, 1st Floor, 200 First Street SW, Rochester, MN, 55905, USA.
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA.
Skeletal Radiol. 2020 Jan;49(1):109-114. doi: 10.1007/s00256-019-03264-3. Epub 2019 Jul 2.
To examine the CT and MRI characteristics of extraneural perineuriomas.
With IRB approval, our institutional imaging database was retrospectively reviewed for cases of pathologically proven extraneural perineuriomas. CT and MRI features were recorded, correlative imaging analyzed, and the electronic medical record cross-referenced.
We identified ten patients [(seven males, three females, mean age 49.4 ± 18.3 years (range, 16-70 years)]. All cases were pathologically confirmed. Nine cases were conventional soft tissue extraneural perineuriomas, including one with "reticular" features and one with histologic features of malignancy; the tenth case contained admixed Schwann cells (hybrid perineurioma/schwannoma). Six out of ten patients underwent CT and ten of ten MRI evaluation. Nine out of ten MRIs were performed with IV contrast. Five lesions were subcutaneous, four intermuscular, and one intramuscular. Mean lesion diameter was 4.3 ± 2.7 cm (range, 0.9-10.2 cm). Nine out of ten lesions were well circumscribed; one had irregular margins. On CT, five of six were hypodense and one isodense compared to skeletal muscle. Most lesions were T1 isointense (5/10) or hypointense (4/10) and T2 hyperintense (7/10) relative to skeletal muscle, and demonstrated solid enhancement (6/9). There was no evidence of muscular denervation on any MRI exam, and a nerve of origin was identified in two out of ten cases.
Extraneural perineuriomas have a distinctly different imaging appearance from intraneural perineuriomas, manifesting as rounded or ovoid soft tissue masses, without evidence of muscular denervation, and usually without an apparent nerve of origin. Because these features mimic other benign and malignant soft tissue lesions, including sarcomas, biopsy or excision is needed for definitive diagnosis.
研究神经外膜周围细胞瘤的 CT 和 MRI 特征。
经机构审查委员会批准,我们对经病理证实的神经外膜周围细胞瘤病例的影像数据库进行了回顾性分析。记录 CT 和 MRI 特征,分析相关影像学表现,并与电子病历进行交叉核对。
共纳入 10 例患者[7 例男性,3 例女性,平均年龄 49.4±18.3 岁(范围 16-70 岁)]。所有病例均经病理证实。9 例为常规软组织神经外膜周围细胞瘤,其中 1 例具有“网状”特征,1 例具有恶性组织学特征;第 10 例为混合性雪旺细胞瘤(神经外膜周围细胞瘤/神经鞘瘤混合瘤)。10 例患者中有 6 例行 CT 检查,10 例行 MRI 检查,其中 9 例行静脉对比增强扫描。10 个病灶中有 5 个位于皮下,4 个位于肌肉间,1 个位于肌肉内。病灶平均直径为 4.3±2.7cm(范围 0.9-10.2cm)。10 个病灶中 9 个边界清楚,1 个边界不规则。CT 上,6 个病灶中有 5 个呈低信号,1 个等信号,与骨骼肌相比。大多数病灶 T1 等信号(5/10)或低信号(4/10),T2 高信号(7/10),实性强化(6/9)。所有 MRI 检查均未见肌肉失神经支配,10 例中有 2 例可识别起源神经。
神经外膜周围细胞瘤的影像学表现与神经内周围细胞瘤明显不同,表现为圆形或卵圆形软组织肿块,无肌肉失神经支配表现,通常无明显起源神经。由于这些特征类似于其他良性和恶性软组织病变,包括肉瘤,因此需要进行活检或切除以明确诊断。