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Clinical, arteriographic and histopathologic analysis of 13 patients with thromboangiitis obliterans and coronary
Insights
Thromboangiitis obliterans (TAO), or Buerger's disease, rarely affects the coronary arteries, even in smokers. Young patients with coronary artery disease (CAD) and smoking as a primary risk factor should be evaluated for TAO.
Area of Science:
- Vascular Surgery
- Cardiology
- Pathology
Background:
- Thromboangiitis obliterans (TAO), also known as Buerger's disease, is a rare inflammatory condition affecting small and medium-sized arteries, predominantly in the limbs.
- While smoking is a known risk factor for TAO and arteriosclerosis, its association with coronary artery disease (CAD) is infrequently reported.
Observation:
- A literature review identified 12 cases of TAO with coronary involvement between 1966 and 2012.
- An additional case presented with central nervous system, myocardial, and large-artery involvement, bringing the total to 13 cases.
- Common symptoms included lower limb claudication and acute thoracic pain.
Findings:
- Histological examination revealed thrombosis with an intact internal elastic lamina and granulocytic infiltration of the intima.
- Coronary angiography demonstrated significant involvement of the left anterior descending and right coronary arteries.
- Treatment strategies comprised coronary bypass, angioplasty, smoking cessation, and anticoagulation, with a 50% complete therapeutic response rate.
Implications:
- This review highlights the uncommon clinical association between TAO and CAD.
- Young patients (<40 years) presenting with CAD and significant smoking history, but lacking other major cardiovascular risk factors, warrant investigation for Buerger's disease.
Abstract:
Smoking is a risk factor for thromboangiitis obliterans (TAO, Buerger's disease) and arteriosclerosis, but there are few cases of coronary heart disease (CAD)-associated Buerger's disease. A literature search for articles in English, Spanish and French published between 1966 and 2012 on patients with coronary involvement and TAO revealed 12 patients. We describe an additional case with involvement of the central nervous system, myocardium and large-diameter proximal arteries. The main clinical manifestations in these 13 cases were lower limb claudication and acute thoracic pain. The histologic findings showed thrombosis with unbroken internal elastic lamina and intimal clusters of granulocytes; coronary angiography revealed predominant involvement of the left anterior descending and right coronary artery. Treatment included coronary bypass procedures, coronary angiopiasty, smoking cessation, and anticoagulant therapy. A complete therapeutic response was observed in half the patients. This review of all published cases of TAO patients with coronary symptoms, together with our patient, demonstrates the rarity of this clinical association. Patients under age 40 with CAD but no prominent cardiovascular risk factors besides smoking should be evaluated for the presence of Buerger's disease.
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