6533b7d9fe1ef96bd126cde6
RESEARCH PRODUCT
Arrhythmic sudden cardiac death in a 3-year-old child with intimal fibroplasia of coronary arteries, aorta, and its branches
Gaspare BecchinaRita PassantinoElisabetta OrlandoGabriella OttoveggioEmiliano MaresiMidulla Rsubject
Malemedicine.medical_specialtyHeart VentriclesFibromuscular dysplasiaPathology and Forensic MedicineSudden cardiac deathPolypsAdventitiaInternal medicinemedicine.arterymedicineFibromuscular DysplasiaHumansVimentinMesenteric arteriesAortaAortabusiness.industryMyocardiumArrhythmias CardiacGeneral Medicinemedicine.diseaseCoronary VesselsImmunohistochemistryActinsCoronary arteriesDeath Sudden CardiacAtheromamedicine.anatomical_structureChild Preschoolcardiovascular systemCardiologyDesminTunica IntimaCardiology and Cardiovascular Medicinebusinessdescription
Abstract We report an unusual case of “arrhythmic” sudden cardiac death in a 3-year-old child who died of ischemic myocardial lesions as a result of intimal fibroplasia of the coronary arteries. Also affected were the aorta and its major branches, whereas renal and mesenteric arteries, celiac trunk, and systemic veins were normal. Histopathologic examination showed severe concentric thickening of intima because of a proliferation of spindle-shaped cells (mesenchymal cells) set in an abundant extracellular matrix. In some vascular segments the intima was densely fibrotic and hyalinized. No significant inflammation, foam cells, cholesterol clefts, or other evidence of atheroma were present. The intimal lesions did not involve the media and/or the adventitia. Immunohistochemical staining of intima showed the proliferating mesenchimal cells to be myofibroblastic. Reactions for vimentin and smooth muscle actin were positive, while those for desmin, myosin, CD34, and Factor VIII were negative.
year | journal | country | edition | language |
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2001-05-10 | Cardiovascular Pathology |