Literature DB >> 25297504

A case of ascending aortic dissection and rupture caused by giant cell arteritis.

Misun Pak1, Shimpei Ito, Masaki Takeda, Nobuhide Watanabe, Hirotomo Sato, Saki Ito, Tomoko Adachi, Takashi Sugamori, Akihiro Endo, Nobuyuki Takahashi, Hiroyuki Yoshitomi, Yutaka Ishibashi, Kazuaki Tanabe.   

Abstract

Giant cell arteritis (GCA) is an autoimmune disease characterized by granulomatous inflammation in the wall of medium-sized and large-sized arteries, and it usually occurs in patients over 50 years of age.(1)) Symptoms are nonspecific, and include fatigue, fever, and headache.(2)) It is occasionally combined with aortic complications, and ruptures resulting in death. These complications occur as late events, usually several years after diagnosis and often after other symptoms have subsided.(3)) Physicians should therefore be alert for complications of the large arteries in GCA. Here we present a case of GCA combined with ascending aortic dissection and rupture 3 weeks after diagnosis.

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Year:  2014        PMID: 25297504     DOI: 10.1536/ihj.14-059

Source DB:  PubMed          Journal:  Int Heart J        ISSN: 1349-2365            Impact factor:   1.862


  3 in total

1.  Aortic dissection and fever: cause or consequence.

Authors:  B Manger; G Schett
Journal:  Z Rheumatol       Date:  2017-08       Impact factor: 1.372

2.  Fever of unknown origin, giant cell arteritis, and aortic dissection.

Authors:  K Hofheinz; S Bertz; J Wacker; G Schett; B Manger
Journal:  Z Rheumatol       Date:  2017-02       Impact factor: 1.372

Review 3.  Fever of unknown origin in aortic dissection.

Authors:  S-M Yuan
Journal:  Z Rheumatol       Date:  2017-05       Impact factor: 1.372

  3 in total

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