一系列骨闪烁扫描阴性但心内膜活检确诊阳性的转甲状腺素淀粉样变性心肌病病例。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Antoine Fraix, Emmanuel Itti, Amira Zaroui, Mounira Kharoubi, Elsa Poullot, Lionel Lerman, Soulef Guendouz, Olivier Huttin, Thibaud Damy, Arnault Galat
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引用次数: 0

摘要

背景:骨闪烁成像(BS)是诊断转甲状腺素淀粉样变性心肌病(ATTR-CM)的准确、无创方法。然而,在现实生活中,一些在 BS 中没有心脏摄取的患者却通过心脏活检确诊为 ATTR-CM。我们回顾性地纳入了在法国ATTR-CM转诊中心确诊的所有患者,这些患者都有BS和心脏活检的数据:结果:在 271 名心脏活检阳性的患者中,有 14 人(5%)在 99mTc-hydroxymethylene diphosphonate BS 检测中未发现心脏摄取。在用99m锝-3,3-二磷酸-1,2-丙二羧酸(DPD)进行第二次BS评估的7名患者中,有4人发现了心脏摄取。对 BS 数据的回顾性复查发现,有四名患者(两名使用 HMDP,两名同时使用两种放射性核素)的心脏摄取率较低。最终,在活检确诊为ATTR-CM的14例患者中,有6例未显示任何心脏放射性示踪剂摄取:结论:对于有心脏淀粉样变性的临床和影像学表现,但在BS中没有心脏放射性示踪剂摄取的患者,心内膜活检可能是确诊ATTR-CM的必要手段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A series of cases of transthyretin amyloid cardiomyopathy with negative bone scintigraphy but a confirmed positive endomyocardial biopsy.

Background: Bone scintigraphy (BS) is established as an accurate, non-invasive method for the diagnosis of transthyretin amyloid cardiomyopathy (ATTR-CM). In a real-life setting, however, some patients with no cardiac uptake on BS turn out to have cardiac-biopsy-confirmed ATTR-CM. We retrospectively included all patients diagnosed at the French Referral Center for ATTR-CM and who had data for BS and a cardiac biopsy.

Results: Of 271 patients with positive cardiac biopsy, 14 (5%) had no cardiac uptake on 99mTc-hydroxymethylene diphosphonate BS. Cardiac uptake was found in four of the seven patients who had a second BS assessment with 99mTc-3,3-diphosphono-1,2-propanodicarboxylic acid (DPD). A retrospective review of the BS data found low cardiac uptake in four patients (two with HMDP and two with both radiotracers). Ultimately, six of the 14 patients with a biopsy-confirmed diagnosis of ATTR-CM did not show any cardiac radiotracer uptake.

Conclusions: An endomyocardial biopsy may be necessary for confirming the diagnosis of ATTR-CM in patients with clinical and imaging signs of cardiac amyloidosis but no cardiac radiotracer uptake in BS.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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