ArticleJournal of cardiology cases2025
Left main compression syndrome caused by pulmonary hypertension due to peripheral pulmonary artery stenosis complicated with moyamoya disease.
Article in Journal of cardiology cases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed, 1 synthesis or guideline pooled it.
- Extracranial vascular association of moyamoya disease: a systematic review and machine learning analysis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026Pooled it
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Authors and funding
8 authors.
Funding
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Abstract
Left main compression syndrome (LMCS) is a disease in which the ostium of the left main coronary artery is compressed between a dilated pulmonary artery and the sinus of Valsalva associated with pulmonary hypertension (PH). The major etiology of LMCS is secondary PH due to congenital heart disease. However, no reports exist regarding LMCS caused by PH due to peripheral pulmonary artery stenosis complicated with moyamoya disease (MMD). We report a case of LMCS caused by PH due to peripheral pulmonary artery stenosis complicated with MMD in a 41-year-old woman who was treated with percutaneous coronary intervention. Learning objective: Left main compression syndrome (LMCS) is a condition in which the main trunk of the left coronary artery is compressed between the dilated pulmonary artery and aorta due to pulmonary hypertension. This paper reports the first case of LMCS due to peripheral pulmonary artery stenosis complicated with moyamoya disease.
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