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谨防患有斯-韦综合征患者出现静脉曲张。

Beware of varicose veins in a patient with sturge-weber syndrome.

作者信息

Mofidi R, Nagy J, Levison R A, Griffiths G D

机构信息

Department of Vascular Surgery, Ninewells Hospital, Dundee, United Kingdom.

出版信息

Ann Vasc Surg. 2007 Sep;21(5):640-4. doi: 10.1016/j.avsg.2007.03.015. Epub 2007 May 29.

Abstract

This report describes the case of a 21-year-old man with a history of Sturge-Weber syndrome and varicose veins. Examination of the left lower limb revealed the presence of significant port-wine staining, and hypertrophy. Duplex examination revealed a severely hypoplastic deep venous system with a tortuous, dilated, long saphenous vein, which was competent and responsible for a significant proportion of venous return from the left lower limb, thus confirming the diagnosis of Klippel-Trenaunay syndrome. The patient was counseled regarding the implications of the diagnosis and was treated conservatively. The association between these two rare syndromes has been previously reported in the nonvascular literature. We believe that features of the Sturge-Weber syndrome or other forms of mesodermal phakomatosis should alert a clinician to the presence of lower limb venous malformations, which will need to be investigated prior to embarking on what could be potentially detrimental venous surgery.

摘要

本报告描述了一名21岁男性患者的病例,该患者有斯-韦综合征和静脉曲张病史。对左下肢的检查发现有明显的葡萄酒色斑和肥大。双功超声检查显示深静脉系统严重发育不全,大隐静脉迂曲、扩张且冗长,该静脉功能正常且承担了左下肢相当比例的静脉回流,从而确诊为克-特综合征。已就该诊断的影响向患者提供了咨询,并给予保守治疗。这两种罕见综合征之间的关联此前已在非血管文献中有所报道。我们认为,斯-韦综合征或其他形式的中胚层错构瘤的特征应提醒临床医生注意下肢静脉畸形的存在,在进行可能有潜在危害的静脉手术之前需要对此进行调查。

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