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Aortic dissection

A Case of Lymphadenitis Mimicking Aortic Dissection in a Patient Diagnosed with Behçet's Disease

DOI: 
10.7727/wimj.2015.395

The Editor,

Sir,

We describe a case of inguinal lymphadenitis mimicking abdominal aortic dissection in a patient diagnosed with Behçet's disease.

Accepted: 
02 Feb, 2016
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e-Published: 31 Mar, 2016

Disclaimer

Manuscripts that are Published Ahead of Print have been peer reviewed and accepted for publication by the Editorial Board of the West Indian Medical Journal. They may appear in their original format and may not be copy edited or formatted in the style guide of this Journal. While accepted manuscripts are not yet assigned a volume, issue or page numbers, they can be cited using the DOI and date of e-publication. See our Instructions for Authors on how to properly cite manuscripts at this stage. The contents of the manuscript may change before it is published in its final form. Manuscripts in this section will be removed once they have been issued to a volume and issue, but will still retain the DOI and date of e-publication.

Rare Seagull Cooing Murmur from Acute Aortic Dissection

Issue: 
DOI: 
10.7727/wimj.2014.244
Pages: 
286–7

ABSTRACT

Accepted: 
31 Oct, 2014
PDF Attachment: 
Journal Sections: 
Journal Authors: 
e-Published: 15 Apr, 2015

Marfan’s Syndrome: Pre-pubertal Aortic Rupture with Left Coronary Artery Aneurysms and Fistulas

Issue: 
DOI: 
10.7727/wimj.2012.233
Pages: 
937–40

ABSTRACT

Aortic dissection and rupture occur in 20–40% of patients with Marfan’s syndrome. This occurs predominantly in the third and fourth decade of life, contributing to the increased morbidity and mortality of this specific group of patients. This is the first known documented case report of prepubertal left coronary sinus rupture with left coronary artery aneurysms with fistulous communication to both the superior vena cava and right superior pulmonary vein, presenting with a continuous murmur.

 

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e-Published: 24 Jun, 2013

Marfan’s Syndrome: Pre-pubertal Aortic Rupture with Left Coronary Artery Aneurysms and Fistulas

DOI: 
10.7727/wimj.2012.233

ABSTRACT


Aortic dissection and rupture occur in 20–40% of patients with Marfan's syndrome. This occurs predominantly in the third and fourth decade of life, contributing to the increased morbidity and mortality of this specific group of patients. This is the first known documented case report of pre-pubertal left coronary sinus rupture with left coronary artery aneurysms with fistulous communication to both superior vena cava and right superior pulmonary vein presenting with a continuous murmur.

PDF Attachment: 
Journal Sections: 
Journal Authors: 
e-Published: 21 Feb, 2013

Pre-published Manuscript

This manuscript has been assigned to a volume and issue but has not yet been published. It is either being edited, typeset or is in the proof stage of publication.
In the pre-published stage, this manuscript may contain statements, opinions, and information that have errors in facts, figures, or interpretation. Any final changes in this manuscript will be made at the time of publication and will be reflected in the final electronic version of the issue. The editors and authors and their respective employees are not responsible or liable for the use of any such inaccurate or misleading data, opinion or information contained in the articles in this section.

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