McKinney A M, Short J, Lucato L, SantaCruz K, McKinney Z, Kim Y
Department of Radiology, University of Minnesota Medical School & Hennepin County Medical Center, Minneapolis 55415, USA.
AJNR Am J Neuroradiol. 2006 Nov-Dec;27(10):2217-20.
Inflammatory myofibroblastic tumor (IMT), Tolosa-Hunt syndrome (THS), and idiopathic hypertrophic pachymeningitis (IHP) seem to be part of a spectrum of disorders that have diverse locations but similar histologic and imaging findings. We report a case of a 50-year-old man presenting with multiple progressive cranial nerves palsies with leptomeningeal cranial nerve enhancement on MRI (II, V1-V3, and X), orbital and infraorbital masses, prominence within the left cavernous sinus, and diffuse dural enhancement. Biopsies of the orbital lesion and infraorbital nerve revealed IMT. The patient's lesions, symptoms, and dural enhancement quickly improved with steroid administration and nearly resolved over multiple subsequent scans over the next few months. This case illustrates a rare case of pseudotumor mimicking a more aggressive appearance that would usually portend a case of malignancy. There is a potential association of IMT, THS, and IHP, which may have existed in a concomitant fashion in this patient. The case also describes the unique finding of enhancement of the cisternal segments of multiple cranial nerves (simulating leptomeningeal malignant involvement), which may be related to inflammatory perineural edema or ischemic neuropathy.
炎性肌纤维母细胞瘤(IMT)、托洛萨-亨特综合征(THS)和特发性肥厚性硬脑膜炎(IHP)似乎是一系列疾病的一部分,这些疾病位置各异,但组织学和影像学表现相似。我们报告一例50岁男性病例,该患者出现多发性进行性颅神经麻痹,MRI显示软脑膜颅神经强化(II、V1-V3和X)、眼眶及眶下肿块、左侧海绵窦突出以及硬脑膜弥漫性强化。眼眶病变和眶下神经活检显示为IMT。患者的病变、症状及硬脑膜强化在给予类固醇治疗后迅速改善,在接下来几个月的多次后续扫描中几乎完全消退。该病例说明了一种罕见的假瘤病例,其表现类似更具侵袭性的病变,通常预示为恶性肿瘤。IMT、THS和IHP之间可能存在关联,在该患者中可能是以合并形式存在。该病例还描述了多个颅神经脑池段强化这一独特发现(模拟软脑膜恶性受累),这可能与炎性神经周水肿或缺血性神经病变有关。