Carlstrom Lucas P, Graffeo Christopher S, Perry Avital, Atkinson John D, Lanzino Giuseppe, Meyer Fredric B, Morris Jonathan M
Department of Neurologic Surgery, Mayo Clinic, Rochester, MN, USA.
Department of Neurologic Surgery, Mayo Clinic, Rochester, MN, USA; Department of Radiology, Mayo Clinic, Rochester MN, USA.
J Clin Neurosci. 2020 Aug;78:128-134. doi: 10.1016/j.jocn.2020.05.051. Epub 2020 Jun 4.
Spinal solitary fibrous tumor/hemangiopericytoma (SFT/HPC) is a rare mesenchymal malignancy. Radiographically, SFT/HPCs have a mutable appearance, with irregular borders, heterogeneous contrast enhancement, and variable but frequently hypointense T2 signal. We report a series of 5 neurosurgically managed spinal SFT/HPCs treated at our institution, with particular attention to 3 lesions demonstrating marked T2-hypointensity and differential diagnosis for the unusual finding of a "T2 dark" spinal lesion. Retrospective chart review of prospectively maintained surgical database, queried by diagnosis and site codes, 2002-2017. Retrospective radiographic review, with initial screening via keyword search of MR reports for "T2" and "hypointense." Four primary and one metastatic spinal SFT/HPCs were operatively treated during the study period (median follow-up 12 months; range 10-92). Three demonstrated marked T2 hypointensity on preoperative MRI, underwent primary resection-GTR in two, STR in one-and have remained progression-free on routine postoperative surveillance. Two patients with isointense lesions recurred within the follow-up period. Radiographic review identified a host of predominantly rare T2-hypointense lesions, including arteriovenous malformation, disk fragmentations, calcific arachnoiditis, calcifying pseudoneoplasm of the neuraxis, cavernoma, cord hemorrhage/acute blood, desmoid, granulocytic sarcoma, pigmented villonodular synovitis, Edheim-Chester, extramedullary hematopoiesis, IgG4-negative inflammatory pseudotumor, idiopathic hypertrophic pachymeningitis, B-cell lymphoma, primary melanoma neoplasm, melanotic schwannoma, meningioma, opacification of the posterior longitudinal ligament, osteoblastoma, osteochondroma, osteosarcoma, and synovial cyst. T2 hypointensity is associated with SFT/HPC, and may be an indicator relative indolence. "Dark" T2 spinal lesions are rare, with a narrow differential populated predominantly by rare entities.
脊柱孤立性纤维瘤/血管外皮细胞瘤(SFT/HPC)是一种罕见的间叶性恶性肿瘤。在影像学上,SFT/HPC表现多样,边界不规则,对比增强不均匀,T2信号可变但常为低信号。我们报告了在我院接受神经外科治疗的5例脊柱SFT/HPC病例系列,特别关注3例显示明显T2低信号的病变以及对“T2暗区”脊柱病变这一不寻常发现的鉴别诊断。通过诊断和部位编码对2002年至2017年前瞻性维护的手术数据库进行回顾性图表审查。进行回顾性影像学审查,最初通过在MR报告中搜索关键词“T2”和“低信号”进行筛查。在研究期间,4例原发性和1例转移性脊柱SFT/HPC接受了手术治疗(中位随访12个月;范围10 - 92个月)。3例在术前MRI上显示明显的T2低信号,2例行初次切除 - 全切,1例行次全切,在术后常规监测中无疾病进展。2例等信号病变患者在随访期内复发。影像学审查发现了许多主要为罕见的T2低信号病变,包括动静脉畸形、椎间盘碎片、钙化性蛛网膜炎、神经轴索钙化性假肿瘤、海绵状血管瘤、脊髓出血/急性血液、硬纤维瘤、粒细胞肉瘤、色素沉着绒毛结节性滑膜炎、埃迪姆 - 切斯特病、髓外造血、IgG4阴性炎性假瘤、特发性肥厚性硬脑膜炎、B细胞淋巴瘤、原发性黑色素瘤、黑色素性神经鞘瘤、脑膜瘤、后纵韧带增厚、骨母细胞瘤、骨软骨瘤、骨肉瘤和滑膜囊肿。T2低信号与SFT/HPC相关,可能是相对惰性的一个指标。“暗区”T2脊柱病变罕见,鉴别诊断范围窄,主要由罕见实体组成。