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Acute coronary syndrome with severe coronary calcification in a patient with pseudo-pseudohypoparathyroidism
Keiichiro Endo1, Takeshi Shimizu1, Yuki Muto1
1Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan.
Insights
Pseudo-pseudohypoparathyroidism (PPHP) can cause severe coronary artery calcification, leading to acute coronary syndrome. This case highlights PPHP as a potential cause of premature heart disease in patients with characteristic physical findings.
Area of Science:
- Endocrinology
- Cardiology
- Genetics
Background:
- Pseudo-pseudohypoparathyroidism (PPHP) is a genetic disorder characterized by physical features and ectopic calcifications.
- Coronary artery disease (CAD) is a significant health concern, often associated with traditional risk factors.
Abstract:
A 40-year-old female with a history of steroid therapy for juvenile rheumatoid arthritis was brought to our hospital because of chest pain. A diagnosis of non-ST elevation myocardial infarction was made, and emergency coronary angiography revealed stenotic lesions with severe calcification in the left anterior descending artery and the right coronary artery. Percutaneous coronary intervention with rotational atherectomy followed by a drug-coated balloon was performed to the lesion in the left anterior descending artery. The patient had characteristic physical findings including short stature, a round face, and 'knuckle-dimple sign'. Whole-body computed tomography showed many ectopic calcifications, indicating Albright's hereditary osteodystrophy. Ellsworth-Howard test revealed that urinary cyclic adenosine monophosphate response was positive, thus a diagnosis of pseudo-pseudohypoparathyroidism (PPHP) was made. Here, we describe a rare case of PPHP complicated by acute coronary syndrome with severely calcified coronary arteries.
Learning Objective:
Pseudo-pseudohypoparathyroidism (PPHP) presents with several characteristic physical findings and ectopic calcifications. Since PPHP involves coronary artery calcification as in the present case, it may be considered as a cause of coronary artery disease.
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