首页> 美国卫生研究院文献>The Pan African Medical Journal >Syndrome canalaire du pied révélant un schwannome du nerf fibulaire superficiel: résultat d’un traitement chirurgical conservateur
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Syndrome canalaire du pied révélant un schwannome du nerf fibulaire superficiel: résultat d’un traitement chirurgical conservateur

机译:根管综合征显示浅表腓神经神经鞘瘤:保守手术治疗的结果

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摘要

We report the case of a 61-year old patient with no particular previous history who complained of pain with paraesthesias at the level of the anterolateral compartment of the left leg irradiating to the dorsal side of the ankle and the foot which lasted over six months. These pains were made worse by effort. Clinical examination showed partial sensitivity deficit and positive Tinel’s sign in the territory of the superficial peroneal nerve (A). Electromyography (EMG) confirmed peroneal nerve involvement with decreased amplitude of sensory potentials. X-ray ruled out the presence of an underlying osteo articular cause (B). Ultrasound objectified well-defined homogeneous tissue formation (C) while MRI showed fusiform mass centered on the nerve with contrast-enhanced T1-weighted hyposignal and T2-weighted hypersignal (D). Conservative surgical resection with sparing of nerve fascicles (E,F) and anatomopathological examination confirmed the diagnosis of benign schwannoma (G). At 1-month follow-up, symptoms had disappeared with sensitivity conservation in the territory of this nerve. The diagnosis of schwannoma is difficult due to the absence of swelling and because schwannoma may mimic entrapment neuropathy, as in the case of our patient. Schwannomas are resectable peripheral nerve tumors. Their prognosis is excellent after adapted surgical treatment with sparing of nerve fascicles.
机译:我们报道了一个没有特定病史的61岁患者,该患者抱怨疼痛持续到六个月以上,感觉异常在左腿的前外侧室水平照射到脚踝和足的背侧。努力使这些痛苦变得更糟。临床检查显示在腓浅神经(A)区域存在部分敏感性不足和Tinel征阳性。肌电图(EMG)证实腓神经受累,感觉电位幅度降低。 X射线检查排除了潜在的骨关节炎原因(B)。超声检查明确定义了均匀的均匀组织形成(C),而MRI显示梭形肿块集中在神经上,同时增强了T1加权的低信号和T2加权的高信号(D)。保守手术切除并保留神经束(E,F)和解剖病理学检查证实了良性神经鞘瘤的诊断(G)。在1个月的随访中,该敏感性区域内的症状消失并保持了敏感性。由于没有肿胀,并且由于神经鞘瘤可能像我们的病人一样,模仿神经鞘神经病,因此很难诊断为神经鞘瘤。神经鞘瘤是可切除的周围神经肿瘤。经过适当的手术治疗并保留神经束后,它们的预后极好。

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