Literature DB >> 21397438

A unique presentation of Takayasu's arteritis in a 39-year-old male with chest pain, vertigo, and blindness.

Mustafa D Nazzal1, Mouchammed Agko, Karen Zingale, Masia Hamdan, Jonathan A Higgins, Paul Clark.   

Abstract

Takayasu's arteritis is a rare form of aortic vasculitis, typically described in young Asian females. In this article, we report a unique presentation of type V Takayasu's arteritis in a Hispanic male. To the best of our knowledge, this is the first case of Takayasu's arteritis presenting with the triad of angina, amaurosis fugax, and subclavian steal syndrome. On diagnostic imaging, he was found to have left subclavian and axillary artery stenosis requiring balloon angioplasty. The patient responded to the combination of medical and surgical treatment with full recovery. Published by Mosby, Inc.

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Year:  2011        PMID: 21397438     DOI: 10.1016/j.jvs.2010.12.059

Source DB:  PubMed          Journal:  J Vasc Surg        ISSN: 0741-5214            Impact factor:   4.268


  1 in total

Review 1.  Amaurosis as an initial presentation of Takayasu arteritis in children.

Authors:  Beatriz Bayardo-Gutiérrez; Marco Antonio Yamazaki-Nakashimada; Ana Luisa Rodríguez-Lozano; Gilberto Gómez-Garza; Francisco Eduardo Rivas-Larrauri; José Alonso Gutiérrez-Hernández; Selma Cecilia Scheffler-Mendoza
Journal:  Rheumatol Int       Date:  2022-04-02       Impact factor: 2.631

  1 in total

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