医学
转甲状腺素
心脏淀粉样变性
淀粉样变性
核医学
放射科
病理
作者
Ali Kibar,Kübra Şahin,Barış İkitimur,Sait Sağer,Haluk Sayman
标识
DOI:10.1097/rlu.0000000000005380
摘要
Amyloidosis is a protein misfolding disorder characterized by the extracellular deposition of insoluble amyloid fibrils, derived from abnormally folded proteins. These fibrils disrupt tissue structure and function, leading to organ dysfunction. The condition encompasses various subtypes, each associated with distinct precursor proteins and clinical manifestations. 99mTc-PYP scintigraphy is used widely and holds significant importance for diagnosis. 68Ga-FAPI is also a promising radiotracer for various diseases. To our knowledge, this is the first case of a patient with hereditary transthyretin amyloidosis with cardiac involvement, which FAPI PET showed diffuse increased myocardial uptake.
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