Data di Pubblicazione:
2009
Abstract:
Heart without HDL.
A 37-year-old man was referred to our lipid clinic because of profound plasma lipid alteration.
He presented large and orange tonsils, hepatosplenomegaly. No corneal opacities
or other ocular abnormalities as well as no nervous system abnormalities were evident.
Haematologic alterations included thrombocytopenia and stomatocytes. HDL and
apolipoprotein A-I concentrations were 4 and 3.9 mg/dL, respectively. Because of a severe
coronary atherosclerosis documented by coronary angiography, he underwent percutaneous
revascularization. Nine months later, he experienced restenosis of the proximal
anterior descending coronary artery and was referred for CABG. The patient was diagnosed
with Tangier disease on the basis of the pathognomonic triad of the disease: HDL
deficiency, low plasma cholesterol concentration accompanied by normal (or even elevated)
triglyceride levels and hyperplastic orange tonsils.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
High density lipoprotein; polidistrectual atherosclerosis; Tangier disease
Elenco autori:
Puntoni, Mariarita
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