血管型Ehlers-Danlos综合征2例及一家系报道并文献复习
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黄建华 E-mail:wxwlq@hotmail.com

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Vascular type Ehlers-Danlos syndrome: a report of 2 cases and a family study with literature review
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    摘要:

    目的:报告血管型Ehlers-Danlos综合征(EDS)患者2例,并总结其中1例5代家系的情况,以增进对该病的认识。
    方法:分析EDS患者的临床资料以及家系成员的特点,就其发病机制及血管型EDS的临床表现、诊断、外科治疗等方面复习文献。
    结果:例1为动脉瘤样扩张自发破裂出血患者,手术时发现血管脆弱易撕裂,术野渗血明显,术后再次出血死亡;例2为左髂动脉瘤破裂出血经介入治疗,病情暂时平稳,但术后多次复发。例2家系中5代13例发病,呈常染色体显性遗传特征。
    结论血管型EDS是一类极为罕见的先天性疾病,其血管合并症常导致患者灾难性后果;外科治疗并发症和病死率高。

    Abstract:

    Objective:To study the pathogenesis, diagnosis and treatment  of vascular Ehlers-Danlos syndrome (EDS).
    Methods:Analysis of the clinical data of 2 patients with EDS and the EDS patients occurred in a fomily. The characteristics of pathogenesis, diagnosis and surgical treatment of EDS were reveiwed.
    Results:One of the EDS patients had spontaneous rupture of aneurysm. At operation, the vessel was found to be fragile and the operative field had marked oozing of blood. Postoperative bleeding led to the patient death. Another case of  EDS underwent interventional treatment several times for thigh hematoma.but bleeding recurred quickly. Pedigree study of case 2 family showed autosomal dominant characteristics.
    Conclusions:Vascular type EDS is a very rare kind of congenital disease.Its vascular complications often lead to disastrous consequences. Surgical therapy has a  high surgical complication and mortality rate.

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王宪伟|刘光强|王伟|欧阳洋|黄建华.血管型Ehlers-Danlos综合征2例及一家系报道并文献复习[J].中国普通外科杂志,2011,20(6):594-598.
DOI:10.7659/j. issn.1005-6947.2011.06.011

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  • 收稿日期:2011-04-25
  • 最后修改日期:2011-06-15
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  • 在线发布日期: 2011-06-15