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首页> 外文期刊>The Tohoku Journal of Experimental Medicine >A case of traumatic high thoracic myelopathy presenting dissociated impairment of rostral sympathetic innervations and isolated segmental sweating on otherwise anhidrotic trunk.
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A case of traumatic high thoracic myelopathy presenting dissociated impairment of rostral sympathetic innervations and isolated segmental sweating on otherwise anhidrotic trunk.

机译:一例外伤性高胸脊髓病,表现为解散的鼻交感神经支配性损伤,以及原发性无汗主干上的孤立的节段性出汗。

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摘要

A 3 year-old boy developed flaccid paraplegia, anesthesia below T3 and impaired vesical control immediately after a car accident. Three months later, the pupils and their pharmacological reactions were normal. Thermal sweating was markedly reduced on the right side of the face, neck, and shoulder and on the bilateral upper limbs, and was absent below T3 except for band like faint sweating on T7 sensory dermatome. The left side of the face, neck and shoulder showed compensatory hyperhidrosis. Facial skin temperature was higher on the sweating left side. Cervico-thoracic MRI suggested almost complete transection of the cord at the levels of T2 and T3 segments. We discussed the pathophysiology of the dissociated impairment of rostral sympathetic innervations and isolated segmental sweating on otherwise anhidrotic trunk.
机译:一名3岁男孩在车祸后立即发展为松弛性截瘫,T3以下麻醉并损害了膀胱控制。三个月后,学生及其药理反应正常。在面部,颈部和肩膀的右侧以及双侧上肢的热汗明显减少,并且在T3以下不存在热汗,除了在T7感觉皮刀上出现带状的淡汗。脸,颈部和肩膀的左侧显示代偿性多汗症。出汗的左侧面部皮肤温度较高。颈胸MRI显示T2和T3节段水平几乎完全切断了脊髓。我们讨论了分离的鼻交感神经支配性损伤和原发性无汗主干的孤立节段性汗液的病理生理。

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