Spontaneous coronary artery dissection in cardiac sarcoidosis

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http://hdl.handle.net/10138/309225

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Kandolin , R , Ekström , K , Simard , T , Hibbert , B , Nery , P , Lehtonen , J , Kupari , M & Birnie , D 2019 , ' Spontaneous coronary artery dissection in cardiac sarcoidosis ' , Oxford medical case reports , vol. 2019 , no. 5 , pp. 212-215 . https://doi.org/10.1093/omcr/omz033

Julkaisun nimi: Spontaneous coronary artery dissection in cardiac sarcoidosis
Tekijä: Kandolin, Riina; Ekström, Kaj; Simard, Trevor; Hibbert, Benjamin; Nery, Pablo; Lehtonen, Jukka; Kupari, Markku; Birnie, David
Muu tekijä: University of Helsinki, HUS Heart and Lung Center
University of Helsinki, Kardiologian yksikkö
University of Helsinki, Kimmo Kontula / Principal Investigator
University of Helsinki, HUS Heart and Lung Center
Päiväys: 2019-05
Kieli: eng
Sivumäärä: 4
Kuuluu julkaisusarjaan: Oxford medical case reports
ISSN: 2053-8855
URI: http://hdl.handle.net/10138/309225
Tiivistelmä: Cardiac sarcoidosis (CS) is increasingly recognized as a cause of diverse cardiac manifestations. Spontaneous coronary artery dissection (SCAD) has emerged as an important cause of acute coronary syndrome especially among young females. The prevalence of sarcoidosis in the causal spectrum of SCAD has not been described before but sarcoidosis is cited as a potential yet rare cause of SCAD. We aimed to examine the frequency and characteristics of SCAD in CS. Searching two prospective CS registries with 481 CS patients, we found only one case of manifest SCAD. She is a 61-year-old female previously diagnosed with endomyocardial biopsy confirmed CS. She presented with chest pain and elevated troponin. Coronary angiogram revealed two-vessel SCAD. Fluorodeoxyglucose positron emission tomography scan showed likely reactivation of CS. The patient was treated with dual antiplatelet therapy and immunosuppression. Repeat angiogram showed complete resolution of the coronary lesions.
Avainsanat: 3121 Internal medicine
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