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持续性孤立性瞳孔散大作为颈内动脉夹层的早期征象:普尔富尔杜·迪·佩蒂综合征。

Persistent isolated mydriasis as an early sign of internal carotid artery dissection: Pourfour du petit syndrome.

作者信息

Sánchez-de la Torre José Ramón, Drake-Pérez Marta, Casado Alfonso, Palacio-Portilla Enrique Jesús, Revilla Marian, Vázquez-Higuera José Luis, Infante Jon

机构信息

Service of Neurology, University Hospital "Marqués de Valdecilla" - IDIVAL - University of Cantabria. Santander, Spain.

Service of Radiology, University Hospital "Marqués de Valdecilla" - IDIVAL, Santander,Spain.

出版信息

Clin Neurol Neurosurg. 2019 Jul;182:70-72. doi: 10.1016/j.clineuro.2019.04.030. Epub 2019 May 1.

Abstract

BACKGROUND

The dissection of the internal carotid artery (ICA) is commonly associated with miosis in Bernard-Horner syndrome (BHS). The presence of mydriasis is exceptional but can occur in the context of Pourfour du Petit syndrome (PDPS), a rare entity opposite of BHS accompanied by eyelid retraction and hyperhidrosis and caused by hyperactivity of the sympathetic cervical chain.

AIM

To report on a case of PDPS as the first manifestation of an ICA dissection.

METHOD

A 54-year-old man presented with isolated left mydriasis with no other abnormalities in the examination. Six months later, he suffered an ischemic stroke in the left middle cerebral artery territory secondary to a left ICA dissection.

RESULTS

The initial study with Intracranial computed tomographic angiography and brain magnetic resonance imaging ruled out compressive cause of the third cranial nerve or structural lesion in the midbrain. The absence of hypersensitivity to Pilocarpine discarded postganglionic parasympathetic involvement.

CONCLUSIONS

In the presence of unilateral mydriasis and once common causes are ruled out an imaging examination of the supra-aortic trunks should be completed, since it could represent the first sign of carotid pathology in the context of PDPS.

摘要

背景

颈内动脉(ICA)夹层常与伯纳德 - 霍纳综合征(BHS)中的瞳孔缩小相关。瞳孔散大的情况较为罕见,但可发生在普尔富尔·迪·佩蒂综合征(PDPS)的背景下,这是一种与BHS相反的罕见病症,伴有眼睑退缩和多汗症,由颈交感神经链亢进引起。

目的

报告一例以PDPS为ICA夹层首发表现的病例。

方法

一名54岁男性出现孤立性左侧瞳孔散大,检查无其他异常。6个月后,他继发于左侧ICA夹层,在左侧大脑中动脉区域发生缺血性卒中。

结果

最初的颅内计算机断层血管造影和脑磁共振成像检查排除了动眼神经受压原因或中脑结构病变。对毛果芸香碱无超敏反应排除了节后副交感神经受累。

结论

在存在单侧瞳孔散大且排除常见病因后,应完成主动脉弓干的影像学检查,因为这可能是PDPS背景下颈动脉病变的首个迹象。

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