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罕见的臂丛神经损伤:伪装成周围神经鞘瘤的血肿。

Unusual brachial plexus lesion: Hematoma masquerading as a peripheral nerve sheath tumor.

作者信息

Krisht Khaled M, Karsy Michael, Shah Lubdha M, Schmidt Meic H, Dailey Andrew T

机构信息

Department of Neurosurgery, Clinical Neurosciences Center, University of Utah, Salt Lake City, Utah 84132, USA.

Department of Radiology, University of Utah, Salt Lake City, Utah 84132, USA.

出版信息

Surg Neurol Int. 2016 Jan 25;7(Suppl 3):S64-6. doi: 10.4103/2152-7806.174889. eCollection 2016.

Abstract

BACKGROUND

Malignant peripheral nerve sheath tumors (MPNSTs) of the brachial plexus have unique radiographic and clinical findings. Patients often present with progressive upper extremity paresthesias, weakness, and pain. On magnetic resonance (MR) imaging, lesions are isointense on T1-weighted and hyperintense on T2-weighted sequences, while also demonstrating marked enhancement on MR studies with gadolinium diethylenetriamine pentaacetic acid. On the basis of their characteristic MR imaging features and rapid clinical progression, two brachial plexus lesions proved to be organizing hematomas rather than MPNST.

METHODS

A 51-year-old male and a 31-year-old female were both assessed for persistent and worsened left-sided upper extremity pain, paresthesias, and weakness. In both cases, the MR imaging of the brachial plexus demonstrated an extraspinal enhancing lesion located within the left C7-T1 neuroforamina.

RESULTS

Although the clinical and radiographic MR features for these 2 patients were consistent with MPNSTs, both lesions proved to be benign organizing hematomas.

CONCLUSIONS

These two case studies emphasize that brachial plexus hematomas may mimic MPNSTs on MR studies. Accurate diagnosis of these lesions is critical for determining the appropriate management options and treatment plans. Delaying the treatment of a highly aggressive nerve sheath tumor can have devastating consequences, whereas many hematomas resolve without surgery. Therefore, if the patient has stable findings on neurological examination and a history of trauma, surgical intervention may be delayed in favor of repeat MR imaging in 2-3 months to re-evaluate the size of the mass.

摘要

背景

臂丛神经的恶性外周神经鞘瘤(MPNST)具有独特的影像学和临床特征。患者常表现为进行性上肢感觉异常、无力和疼痛。在磁共振(MR)成像上,病变在T1加权像上呈等信号,在T2加权像上呈高信号,同时在使用钆喷酸葡胺的MR检查中显示明显强化。基于其特征性的MR成像特征和快速的临床进展,两个臂丛神经病变被证实为机化性血肿而非MPNST。

方法

一名51岁男性和一名31岁女性均因左侧上肢持续性疼痛、感觉异常和无力加重而接受评估。在这两个病例中,臂丛神经的MR成像均显示一个位于左侧C7 - T1神经孔内的椎管外强化病变。

结果

尽管这两名患者的临床和MR影像学特征与MPNST相符,但两个病变均被证实为良性机化性血肿。

结论

这两个病例研究强调,臂丛神经血肿在MR研究中可能会模仿MPNST。准确诊断这些病变对于确定合适的管理方案和治疗计划至关重要。延迟治疗高度侵袭性的神经鞘瘤可能会产生毁灭性后果,而许多血肿无需手术即可消退。因此,如果患者在神经系统检查中表现稳定且有外伤史,手术干预可能会延迟,以便在2 - 3个月后重复进行MR成像以重新评估肿块大小。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e26/4743268/55fc8f394d69/SNI-7-64-g001.jpg

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