Literature DB >> 1997074

Innominate artery involvement in type IV Ehlers-Danlos syndrome.

A Valverde1, J F Tricot, B de Crepy, H Bakdach, K Djabbari.   

Abstract

We report two cases of innominate artery involvement in patients with Ehlers-Danlos syndrome. In the first patient, spontaneous dissection of the innominate artery was treated successfully. In the other, the patient died of spontaneous rupture of the innominate artery in the early postoperative course after operation for aneurysm of the celiac artery. Arterial complications occurring in Ehlers-Danlos syndrome are rare but pose difficult diagnostic and therapeutic problems for the vascular surgeon due to arterial wall fragility.

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Year:  1991        PMID: 1997074     DOI: 10.1007/BF02021776

Source DB:  PubMed          Journal:  Ann Vasc Surg        ISSN: 0890-5096            Impact factor:   1.466


  3 in total

Review 1.  Spontaneous common iliac arteries rupture in Ehlers-Danlos syndrome type IV: report of two cases and review of the literature.

Authors:  K Habib; M A Memon; D A Reid; B J Fairbrother
Journal:  Ann R Coll Surg Engl       Date:  2001-03       Impact factor: 1.891

2.  Aneurysm of the innominate artery with aberrant origin of the left carotid artery. Case report.

Authors:  O Villegas-Cabello; D A Cooley
Journal:  Tex Heart Inst J       Date:  1996

3.  Innominate truncal and arch blowout with left hemiparesis and right hemothorax followed by delayed cheese-wire perforation of innominate graft.

Authors:  Pankaj Kaul; Rodolfo Paniagua
Journal:  J Cardiothorac Surg       Date:  2013-04-23       Impact factor: 1.637

  3 in total

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