Literature DB >> 24570509

Percutaneous coronary intervention in a case of afibrinogenemia.

Homa Falsoleiman1, Mehdi Hasanzadeh Daloee, Mashalla Dehghani, Atoosheh Rohani, Baktash Bayani.   

Abstract

Congenital afibrinogenemia is a rare autosomic recessive blood disorder. A 30-year-old lady, known to have congenital afibrinogenemia, presented with acute anterior myocardial infarction. We managed her with dual antiplatelet therapy and atorvastatin, but her chest pain did not subside and she was transferred to the catheterization laboratory. A proximal left anterior descending artery occlusion was crossed with a floppy wire. Angioplasty was performed successfully with a bare metal stent, and her symptoms resolved completely.

Entities:  

Keywords:  Afibrinogenemia; angioplasty; blood coagulation disorders; inherited; myocardial infarction; stents

Mesh:

Substances:

Year:  2013        PMID: 24570509     DOI: 10.1177/0218492312455180

Source DB:  PubMed          Journal:  Asian Cardiovasc Thorac Ann        ISSN: 0218-4923


  2 in total

1.  Combined life-threatening thromboses and hemorrhages in a patient with afibrinogenemia and antithrombin deficiency.

Authors:  S Le Quellec; A Desjonqueres; L Rugeri; H Desmurs Clavel; F Farhat; L Mechtouff; Y Dargaud
Journal:  Thromb J       Date:  2018-04-04

2.  Endovascular Treatment for Lower-extremity Arterial Thrombosis in a Patient with Congenital Afibrinogenemia and a History of Bleeding Complications.

Authors:  Daisuke Hiramatsu; Yoshito Ogihara; Takeshi Matsumoto; Kei Sato; Akihiro Takasaki; Tairo Kurita; Ryuji Okamoto; Hideo Wada; Kaoru Dohi
Journal:  Intern Med       Date:  2021-07-30       Impact factor: 1.271

  2 in total

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