医学
转甲状腺素
心脏淀粉样变性
淀粉样变性
闪烁照相术
淀粉样蛋白(真菌学)
内科学
病理
分布(数学)
内分泌学
心肌病
突变
淀粉样多发性神经病
心力衰竭
淀粉样纤维
作者
Yuyoung Kim,Jong-Ho Nam,Kyoungjune Pak,Jung Hyun Choi
标识
DOI:10.1097/rlu.0000000000006289
摘要
We describe a case of a 76-year-old man with genetically confirmed hereditary transthyretin amyloidosis (hATTR) due to a pathogenic TTR variant, c.97_99dup (p.Met33dup), with possible coexisting amyloid light-chain (AL) amyloidosis. Serial Technetium-99m 2,3-dicarboxypropane-1,1-diphosphonate Tc-99m DPD) scintigraphy revealed persistent grade 3 myocardial uptake but minimal extracardiac tracer accumulation in the skeletal system and intestines. Despite similar or higher heart-to-contralateral (H/CL) ratios, other patients did not exhibit this pattern, underscoring the atypical nature of the observed findings in this case. This case highlights a rare myocardial-predominant uptake phenotype, which may offer insight into the distribution of bone-avid tracers in cardiac amyloidosis.
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