左侧运动根C7硬膜内-髓外海绵状血管瘤1例报告及文献更新。

J Rachinger, R Buslei, T Engelhorn, A Doerfler, C Strauss
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引用次数: 18

摘要

目的:脊柱硬膜内-髓外海绵状瘤是一种罕见的病变,迄今为止仅报道了21例。由于其罕见性和特殊性,诊断往往很困难。我们报告一个额外的病例硬膜内-髓外海绵瘤的脊柱。患者:56岁男性,入院前两周出现左肩疼痛和累及整个脊柱的急性疼痛。无运动障碍,但右侧远端c8 -皮节有感觉减退。MRI显示硬膜内-髓外,C6水平的扩张性病变,在T(1)和T(2)加权图像上表现为高信号。铁血黄素边缘和对比增强均未见。结果:手术中,左运动根C7附着的血肿和红色浆果样肿瘤被切除。没有新的神经功能障碍,手术后几周内肩部和背部疼痛消失。组织病理学诊断为海绵状血管瘤。结论:患者的症状是由直接神经压迫和脊髓出血引起的,最可能是脊髓SAH。由于没有特征性的含铁血黄素环,并且在T(1)和T(2)加权MR扫描中表现为高强度,因此很难对出血进行放射诊断和病变分类。尽管它们很少见,但在有自发性症状的患者中,脊髓SAH和/或神经压迫综合征海绵状血管瘤必须被认为是一个潜在的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intradural-extramedullary cavernous hemangioma of the left motor root C7--case report and update of the literature.

Objective: Intradural-extramedullary cavernomas of the spine are rare lesions with only 21 published cases to date. Due to their rareness and special characteristics diagnosis often is difficult. We report on an additional case of an intradural-extramedullary cavernoma of the spine.

Patient: A 56-year-old male presented with left shoulder pain and acute onset of pain affecting the whole spinal column two weeks prior to admission. There were no motor deficits, but a hypesthesia corresponding to the right distal C8-dermatome. MRI revealed an intradural-extramedullary, expansive lesion at the level of C6 with a hyperintense appearance in both T (1)- and T (2)-weighted images. Neither a hemosiderin rim nor contrast enhancement was visible.

Results: During surgery a hematoma and a reddish, berry-like tumor adherent to the left motor root C7 were removed. There were no new neurological deficits, and shoulder and back pain resolved within a few weeks after surgery. Histopathologically a cavernous hemangioma was diagnosed.

Conclusions: The patient's symptoms were caused both by direct nerve compression and by spinal hemorrhage, most likely spinal SAH. As there was no characteristic hemosiderin rim and due to the hyperintense appearance in T (1)- and T (2)-weighted MR scans, a radiological diagnosis of hemorrhage and classification of the lesion was difficult. Despite their rareness, in patients with signs of spontaneous, spinal SAH and/or nerve compression syndromes cavernous hemangiomas have to be considered as a potential cause.

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Zentralblatt Fur Neurochirurgie
Zentralblatt Fur Neurochirurgie 医学-神经科学
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