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[面部血管瘤、后颅窝畸形和颈-椎发育不全联合表现(帕斯卡-卡斯特罗维霍综合征II型):2例新病例报告]

[Joint presentation of facial hemangioma, posterior fossa malformation, and carotid-vertebral hypoplasia (Pascual-Castroviejo syndrome II): report of 2 new cases].

作者信息

Torres-Mohedas J, Verdú A, Vidal B, Jadraque R

机构信息

Unidad de Neuropediatría, Servicio de Pediatría, Hospital de Móstoles, Río Júcar, s/n. E-28935 Móstoles, Madrid.

出版信息

Rev Neurol. 2001;32(1):50-4.

Abstract

INTRODUCTION

The association of external capillary hemangiomas with intracranial malformations (vascular or nonvascular) was first described by Pascual-Castroviejo in 1978. The commonest anomalies found included: Dandy-Walker syndrome, cerebellar hypoplasia, arterial angiomas and alterations in the origin or distribution of the main cerebral arteries. In 1996 the same author named it the 'hemangiovascular complex syndrome'. The syndrome association is very similar, perhaps even identical, to that recently described in the English literature under the heading of PHACE.

CLINICAL CASES

We describe two new cases of facial hemangioma, Dandy-Walker type posterior fossa malformation and hypoplasia of the carotid-vertebral trunk ipsilateral to the facial hemangioma. The first patient, a three year old girl had needed a ventriculo-peritoneal shunt for hydrocephalus secondary to a Dandy-Walker malformation. During the third month she had severe symptoms of laryngeal obstruction due to the angiomatous lesion and was satisfactorily treated with corticosteroids. At the present time her psychomotor development seems normal on neurological examination and evaluation. The second patient, a thirteen year old boy, besides showing the characteristic features of this syndrome also had attention-deficit hyperactivity and clumsy movements. In both cases the facial hemangioma was present at birth and gradually became smaller although it did not disappear completely.

CONCLUSION

It is important to know about this neurocutaneous syndrome to avoid confusion with similar conditions such as the Sturge-Weber syndrome, so as to carry out suitable clinical investigations: cerebral magnetic resonance, angio-resonance of the intracranial vessels and supra-aortic trunks, arteriography, echocardiography and ophthalmological assessment and to prevent signs of upper respiratory tract obstruction which may be very serious.

摘要

引言

1978年,帕斯夸尔 - 卡斯特罗维霍首次描述了外部毛细血管瘤与颅内畸形(血管性或非血管性)之间的关联。发现的最常见异常包括:丹迪 - 沃克综合征、小脑发育不全、动脉血管瘤以及大脑主要动脉起源或分布的改变。1996年,同一位作者将其命名为“血管 - 血管瘤复合综合征”。该综合征关联与最近英文文献中以PHACE为题描述的综合征非常相似,甚至可能相同。

临床病例

我们描述了两例新的面部血管瘤病例,丹迪 - 沃克型后颅窝畸形以及与面部血管瘤同侧的颈 - 椎干发育不全。首例患者是一名三岁女孩,因丹迪 - 沃克畸形继发脑积水,需要进行脑室 - 腹腔分流术。在第三个月时,她因血管瘤病变出现严重的喉梗阻症状,经皮质类固醇治疗后情况良好。目前,经神经学检查和评估,她的精神运动发育似乎正常。第二例患者是一名十三岁男孩,除了具有该综合征的特征外,还患有注意力缺陷多动障碍和动作笨拙。在这两个病例中,面部血管瘤均在出生时就存在,尽管没有完全消失,但逐渐变小。

结论

了解这种神经皮肤综合征很重要,以避免与类似疾病如斯特奇 - 韦伯综合征混淆,从而进行适当的临床检查:脑部磁共振成像、颅内血管和主动脉弓干的血管磁共振成像、动脉造影、超声心动图以及眼科评估,并预防可能非常严重的上呼吸道梗阻迹象。

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