Literature DB >> 11668374

Rare manifestation of abdominal aortic aneurysm and popliteal aneurysm in a patient with Marfan's syndrome: a case report.

B Wolfgarten1, I Krüger, M Gawenda.   

Abstract

A 37-year-old patient with back pain and somatomegaly was found to have a penetrating aneurysm of sections IV and V of the abdominal aorta. Results of a family history and clinical examination confirmed suspicions of Marfan's syndrome. Further angiologic studies depicted an aneurysmatic dilatation of the left popliteal artery. Aneurysmatic dilatations are primarily located in sections I and II of the thoracic aorta, whereas aneurysms in sections IV and V are much rarer. The rare combination of an abdominal aortic aneurysm and left-sided popliteal aneurysm accompanying Marfan's syndrome is presented.

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Year:  2001        PMID: 11668374     DOI: 10.1177/153857440103500118

Source DB:  PubMed          Journal:  Vasc Surg        ISSN: 0042-2835


  7 in total

1.  Endothelial dysfunction and compromised eNOS/Akt signaling in the thoracic aorta during the progression of Marfan syndrome.

Authors:  A W Y Chung; K Au Yeung; S F Cortes; G G S Sandor; D P Judge; H C Dietz; C van Breemen
Journal:  Br J Pharmacol       Date:  2007-03-05       Impact factor: 8.739

2.  Abdominal aortic aneurysms, or a relatively large diameter of non-aneurysmal aortas, increase total and cardiovascular mortality: the Tromsø study.

Authors:  Signe Helene Forsdahl; Steinar Solberg; Kulbir Singh; Bjarne K Jacobsen
Journal:  Int J Epidemiol       Date:  2009-11-05       Impact factor: 7.196

3.  Patient with Marfan Syndrome and a Novel Variant in FBN1 Presenting with Bilateral Popliteal Artery Aneurysm.

Authors:  Ahmed Mohammad; Haytham Helmi; Paldeep S Atwal
Journal:  Case Rep Genet       Date:  2018-03-29

4.  Ruptured popliteal artery aneurysm in a patient with a clinical diagnosis of Marfan syndrome.

Authors:  Gabriel Paiva Duarte; Jorge Ribeiro da Cunha
Journal:  J Vasc Bras       Date:  2020-10-16

5.  Autosomal dominant Marfan syndrome caused by a previously reported recessive FBN1 variant.

Authors:  Eline Overwater; Rifka Efrat; Daniela Q C M Barge-Schaapveld; Phillis Lakeman; Marjan M Weiss; Alessandra Maugeri; J Peter van Tintelen; Arjan C Houweling
Journal:  Mol Genet Genomic Med       Date:  2018-11-28       Impact factor: 2.183

6.  Successful repair of a popliteal aneurysm with saphenous vein graft in a patient with Marfan syndrome.

Authors:  Kate Xin Peng; Victor J Davila; Richard J Fowl
Journal:  J Vasc Surg Cases Innov Tech       Date:  2019-09-17

7.  A Case of an Abdominal Aortic Dissection in a Hemodynamically Stable Marfan Syndrome Patient Presenting without Pain.

Authors:  Hussein Al-Mohamad; Kara Stout; Taryn Bolling; Ronald Walsh
Journal:  Case Rep Cardiol       Date:  2020-02-23
  7 in total

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