对接受无症状变异 TTR 携带者肝脏的家族性 ATTR 淀粉样变性患者进行早期诊断和管理。
Early diagnosis and management of patients with familial ATTR amyloidosis receiving livers from asymptomatic variant TTR carriers.
出版信息
Amyloid. 2011 Sep;18(3):172-3. doi: 10.3109/13506129.2011.594822. Epub 2011 Jul 21.
PMID:21774739
Abstract
The possibility of a patient with familial ATTR amyloidosis receiving a liver from an asymptomatic variant TTR carrier is remote [corrected].However, in 2008, it was reported that this unlikely event occurred in a patient in Portugal. We report our protocol for early diagnosis and management of this entity.
摘要
携带无症状变异 TTR 蛋白的家族性 ATTR 淀粉样变性患者接受肝脏移植的可能性极小[已更正]。然而，2008 年有报道称，葡萄牙的 1 例患者发生了这种不太可能的事件。我们报告了这种疾病的早期诊断和管理方案。
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