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Scleroderma and coronary artery disease: a case report
Jomal Mathew1, Vir Singh Negi, Jayaraman Balachander
1Department of Medicine, JIPMER, Puducherry, India. mathewjomal@yahoo.co.in
Insights
This case study highlights a rare instance of scleroderma combined with ischemic heart disease in a 35-year-old woman. The patient showed evidence of myocardial infarction and significant coronary artery disease.
Area of Science:
- Cardiology
- Rheumatology
- Internal Medicine
Background:
- Scleroderma is a chronic autoimmune disease characterized by hardening and tightening of the skin and connective tissues.
- Ischemic heart disease (IHD) encompasses conditions caused by narrowed heart arteries, leading to reduced blood flow to the heart muscle.
- The co-occurrence of scleroderma and IHD is infrequent, posing diagnostic and therapeutic challenges.
Observation:
- A 35-year-old woman presented with symptoms suggestive of cardiac compromise.
- Electrocardiogram (ECG) indicated a history of inferior wall myocardial infarction.
- Coronary angiography was performed to assess for coronary artery disease.
Findings:
- The patient was diagnosed with scleroderma, a rare autoimmune connective tissue disease.
- Significant coronary artery disease was identified during coronary angiography.
- The findings suggest a potential link between scleroderma and the development of ischemic heart disease.
Implications:
- This case underscores the importance of considering cardiovascular complications in patients with scleroderma.
- Early recognition and management of ischemic heart disease in scleroderma patients may improve outcomes.
- Further research is warranted to elucidate the pathophysiological mechanisms connecting scleroderma and coronary artery disease.
Abstract:
We present the case of a 35-year-old woman presenting with the rare combination of scleroderma and ischemic heart disease. Her ECG suggested old inferior wall myocardial infarction. Coronary angiography revealed significant coronary artery disease.
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