# Thrombolysis in spontaneous coronary artery dissection: a case report of acute catastrophic dissection requiring coronary artery bypass surgery and delayed heart transplant in a young woman with fibromuscular dysplasia

## TL;DR

A young woman with fibromuscular dysplasia experienced severe coronary artery dissection, requiring emergency surgery and a heart transplant two years later.

## Contribution

This case highlights the rare and complex progression of SCAD with FMD requiring multiple interventions, including heart transplant.

## Key findings

- SCAD involving multiple coronary arteries led to cardiogenic shock and required emergent CABG.
- The patient's prolonged course with FMD and complications ultimately necessitated a heart transplant after two years.
- This case demonstrates the need for long-term management strategies in SCAD with FMD.

## Abstract

Spontaneous coronary artery dissection (SCAD) is a rare condition characterized by a tear in the coronary artery wall and is often associated with fibromuscular dysplasia (FMD). It is unclear whether SCAD with FMD represents a progressive pathology that leads to both acute and chronic complications, including myocardial damage and advanced heart failure.

A 43-year-old woman with chest pain was initially diagnosed with ST-elevation myocardial infarction and later found to have SCAD involving the left main, left anterior descending, and left circumflex arteries. She developed cardiogenic shock requiring emergent coronary artery bypass surgery (CABG). She had a prolonged course with underlying FMD, superior mesenteric artery dissection, multiple decompensated heart failure, and cardiogenic shock ultimately requiring a heart transplant after 2 years.

Revascularization in SCAD is not well defined with limited data. The incidence of cardiogenic shock is 1.2%–15.9%. There are case reports on mechanical circulatory support (MCS), CABG, and heart transplantation. This case is unique requiring MCS and CABG with SCAD and heart transplant after 2 years.