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首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Complete response to steroids in dural inflammatory pseudotumor associated with Still's disease
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Complete response to steroids in dural inflammatory pseudotumor associated with Still's disease

机译:对与Still病相关的硬脑膜炎性假瘤中的类固醇完全反应

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摘要

We report a unique case of a dural-based inflammatory pseudotumor (IPT) arising in the left cavernous sinus of a patient with a history of juvenile Still's disease. The patient presented with hemi-facial paresthesias, dull, constant headaches, and transient episodes of sharp pain along the temporalis region. Treatment with oral steroid therapy resulted in complete regression of the lesion and accompanied neuralgia symptoms. Because intracranial IPT can mimic meningiomas both clinically and radiographically and can be associated with systemic arthritic diseases, neurosurgeons should be familiar with this entity in order to avoid unnecessary radical surgery and alternatively consider a tapering course of steroid therapy.
机译:我们报告了硬脑膜炎性假瘤(IPT)的一个独特的案例,该病例发生在有史蒂尔氏病史的患者的左海绵窦中。患者表现出半面部感觉异常,钝痛,持续头痛以及沿颞叶区域的剧烈疼痛的短暂发作。口服类固醇激素疗法可导致病变完全消退并伴有神经痛症状。由于颅内IPT可以在临床和影像学上模拟脑膜瘤,并且可以与全身性关节炎相关联,因此神经外科医生应对此实体熟悉,以避免不必要的根治性手术,或者考虑减少类固醇疗法的疗程。

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