Screening for fibromuscular dysplasia after spontaneous coronary artery dissection unmasks a massive right renal artery aneurysm requiring ex vivo surgical resection and autotransplantation.

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Tác giả: Robert Graham, Munish Heer, Nikhil Mahajan, Lucy McGrath-Cadell

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: England : BMJ case reports , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 708684

 Spontaneous coronary artery dissection (SCAD) is an increasingly recognised cause of acute coronary syndrome predominantly affecting women (>
 90% of cases) that is frequently associated with other arteriopathies, such as fibromuscular dysplasia (FMD) and migraine. We present a case of multi-vessel SCAD in a woman in her 40s presenting with myocardial infarction in whom incidental widespread FMD was found, including a massive right renal artery aneurysm requiring ex vivo resection, repair and autotransplantation. The case underscores the need for routine angiographic screening for FMD, which has a shared genetic risk with SCAD, and is associated with aneurysms, stenoses and hypertension.
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