活组织检查证实遗传性甲状腺转蛋白Ala117Ser心脏淀粉样变性的二膦酸亚甲基显像阴性1例

Q4 Medicine Cardiology Plus Pub Date : 2023-07-01 DOI:10.1097/cp9.0000000000000058
Zejia Wu, Shuang Xia, Dunliang Ma, Liwen Li
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引用次数: 0

摘要

99m tc -焦磷酸显像(99m Tc-PYP)对转甲状腺素型心脏淀粉样变性(atr - ca)的诊断具有高度的敏感性和特异性。常用的替代示踪剂有99m tc -3,3-二膦-1,2-丙二羧酸(99m Tc-DPD)和99m tc -二膦酸羟亚甲基(99m Tc-HMDP)。一位61岁的中国男性表现出左心室肥厚的迹象。基因检测显示为杂合型转甲状腺素Ala117Ser突变。使用99m tc -二膦酸亚甲基显像未能显示心肌摄取。五个月后,患者接受了永久性心脏起搏器植入手术。不定期使用他法米地,患者于2年后死亡。99m tc -二膦酸亚甲基可能不适合用于甲状腺转视蛋白Ala117Ser突变的atr - ca患者的诊断。
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Negative methylene diphosphonate scintigraphy in biopsy-confirmed hereditary transthyretin Ala117Ser cardiac amyloidosis: a case report
99m Tc-pyrophosphate ( 99m Tc-PYP) scintigraphy is highly sensitive and specific for the diagnosis of transthyretin cardiac amyloidosis (ATTR-CA). Commonly used alternative tracers included 99m Tc-3,3-diphosphono-1,2-propanodicarboxylic acid ( 99m Tc-DPD) and 99m Tc-hydroxymethylene diphosphonate ( 99m Tc-HMDP). A 61-year-old Chinese man presented with signs indicative of left ventricular hypertrophy. Genetic testing revealed heterozygous transthyretin Ala117Ser mutation. Scintigraphy using 99m Tc-methylene diphosphonate failed to show myocardial uptake. Five months later, the patient underwent permanent pacemaker implantation. Tafamidis was used irregularly, and the patient died 2 years later. 99m Tc-methylene diphosphonate may not be appropriate for diagnostic use in ATTR-CA patient with transthyretin Ala117Ser mutation.
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CiteScore
0.50
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0.00%
发文量
24
审稿时长
32 weeks
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