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Published on: February 22, 2013
The Simultaneity of Coronary Artery Ectasia and Intracranial Arterial Dolichoectasia: A Rare Case Report
Harith Adnan Alataby1, George Freg1, Rana Alzakhari1
1Department of Medicine, Richmond University Medical Center, Staten Island, NY 10310, USA.
Insights
This case study highlights the rare co-occurrence of coronary artery ectasia (CAE) and intracranial arterial dolichoectasias (IADEs). Management focuses on conservative treatment of risk factors and antiplatelet/anticoagulant agents.
Area of Science:
- Cardiology
- Neurology
- Vascular Medicine
Background:
- Coronary artery ectasia (CAE) involves abnormal coronary artery dilatation, potentially leading to ischemia and thrombosis.
- Intracranial arterial dolichoectasias (IADEs) are dilatations and elongations of cerebral arteries, causing neurological complications.
- Coexistence of CAE and IADEs is exceptionally rare.
Observation:
- A 60-year-old female presented with chest pain and later dizziness.
- Coronary angiography revealed severe ectasia and stenosis in multiple coronary arteries.
- Head CT angiography demonstrated severe IADEs in the vertebrobasilar system and intracranial arteries.
Findings:
- The patient exhibited severe, multifocal CAE and IADEs.
- Pathological mechanisms may involve medial elastic tissue rarefaction and internal elastic lamina degeneration.
- Management was primarily conservative, addressing risk factors and utilizing antiplatelet/anticoagulant therapy.
Implications:
- This case underscores the importance of considering systemic vascular abnormalities.
- Conservative management is typical, but interventional options like angioplasty may be considered.
- Further research into the shared pathophysiology of CAE and IADEs is warranted.
Abstract:
In the present study, we report a case of multiple coronary artery ectasias (CAE) and multiple intracranial arterial dolichoectasias (IADEs). A 60-year-old female presented to the emergency department twice with chest pain and mild elevation of troponin and T-wave changes. Peripheral coronary angiography showed severe ectasia and stenosis of certain segments of the left main coronary artery (LMCA), left anterior descending (LAD), first obtuse marginal (OM1), distal left circumflex (LCX), and bilateral subclavian arteries. The patient was treated medically. Two weeks later, she presented with dizziness. Head computerized tomography (CT) angiography showed severe IADE involving the vertebrobasilar system, intracranial internal carotid arteries, and bilateral middle cerebral arteries. No neurovascular intervention was performed due to the complexity of the findings. CAE is an abnormal dilatation of a coronary artery segment of at least 1.5 times the size of a normal coronary artery. The slow flow phenomenon may lead to ischemia and thrombosis, which can result in acute coronary syndrome. IADE comprises a dilatation and elongation of the arteries that affects both the anterior and posterior cerebral circulation, often causing neurological complications such as ischemic stroke, intracranial hemorrhage, or compression of surrounding neural structures. We report this case due to the rarity of coexisting IADE and CAE. A rarefaction of elastic tissue of the media with degeneration of the internal elastic lamina, in addition to matrix metalloproteinase dysfunction, is a common pathological mechanism for this condition. The management of CAE and IADE is mostly conservative, essentially treating the risk factors and administering antiplatelet and anticoagulant agents. In some patients, angioplasty vs. surgical treatment may be applied.
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