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攻克隐匿性黑桃:心尖部变异型肥厚型心肌病的诊断、随访、预后及各种关联综述

"Acing" the Hidden Spade: Review of Diagnosis, Follow-up, Prognosis, and Various Associations of Apical Variant Hypertrophic Cardiomyopathy.

作者信息

Patel Hiren, Ko Ko Nway L, Kumar Sundeep, Gros Bernard

机构信息

Internal Medicine, University of Central Florida College of Medicine, Orlando, USA.

出版信息

Cureus. 2019 Jan 29;11(1):e3979. doi: 10.7759/cureus.3979.

DOI:10.7759/cureus.3979
PMID:30967979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6440565/
Abstract

Apical variant hypertrophic cardiomyopathy (AHCM) is a known entity since its first introduction by Sakamoto and Yamaguchi. However, unlike classical hypertrophic cardiomyopathy (HCM), it is less explored in terms of its associated diagnosis and long-term outcomes. Through this case presentation, we aim to have an in-depth review to help physicians identify and better understand several aspects of AHCM. Given the increased availability and utilization of high precision cardiac imaging modalities, apical septal hypertrophic cardiomyopathy will increasingly be recognized as a distinct, clinically significant variant of classical HCM. Contrast echocardiogram is the most effective and diagnostic study when performed in the right setting with high suspicion on clinical examination findings and typical electrocardiogram (EKG) findings. Cardiac magnetic resonance imaging (MRI) has equal diagnostic yield as a contrast echocardiogram. It is associated with a wide spectrum of presentation ranging from asymptomatic course with incidental findings on imaging to rarely being associated with ventricular arrhythmia. The question of utility of implantable defibrillators in individuals, particularly without any underlying arrhythmias, remains unexplained and needs further evidence-based guidance.

摘要

自从坂本和山口首次提出心尖部变异型肥厚型心肌病(AHCM)以来,它已是一个已知的病症。然而,与经典肥厚型心肌病(HCM)不同,在其相关诊断和长期预后方面,对它的研究较少。通过本病例报告,我们旨在进行深入回顾,以帮助医生识别并更好地理解AHCM的几个方面。鉴于高精度心脏成像模式的可及性和应用增加,心尖部间隔肥厚型心肌病将越来越被视为经典HCM的一种独特的、具有临床意义的变异型。当在临床检查结果和典型心电图(EKG)结果高度可疑的合适情况下进行时,对比超声心动图是最有效和最具诊断性的检查。心脏磁共振成像(MRI)的诊断率与对比超声心动图相当。它的表现范围广泛,从影像学检查偶然发现的无症状病程到很少与室性心律失常相关。植入式除颤器在个体中的效用问题,特别是在没有任何潜在心律失常的个体中,仍然无法解释,需要进一步基于证据的指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e4c/6440565/2319884516bb/cureus-0011-00000003979-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e4c/6440565/13287d46aa6f/cureus-0011-00000003979-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e4c/6440565/2319884516bb/cureus-0011-00000003979-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e4c/6440565/13287d46aa6f/cureus-0011-00000003979-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e4c/6440565/2319884516bb/cureus-0011-00000003979-i02.jpg

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本文引用的文献

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Enlarged left atrium, atrial fibrillation and adverse outcome in hypertrophic cardiomyopathy: is there a difference between apical and non-apical phenotype?
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Impact of atrial fibrillation on the clinical course of apical hypertrophic cardiomyopathy.心房颤动对心尖肥厚型心肌病临床病程的影响。
Heart. 2017 Oct;103(19):1496-1501. doi: 10.1136/heartjnl-2016-310720. Epub 2017 Apr 20.
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Apical Hypertrophic Cardiomyopathy Among Non-Asians: A Case Series and Review of the Literature.非亚洲人群中的肥厚型心肌病:病例系列及文献综述
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Apical hypertrophic cardiomyopathy presenting as acute coronary syndrome.表现为急性冠状动脉综合征的肥厚型心肌病
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Hypertrophic cardiomyopathy apical variant.肥厚型心肌病心尖部变异型
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Risk of death in long-term follow-up of patients with apical hypertrophic cardiomyopathy.心尖肥厚型心肌病患者长期随访的死亡风险。
Am J Cardiol. 2013 Jun 15;111(12):1784-91. doi: 10.1016/j.amjcard.2013.02.040. Epub 2013 Mar 27.
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2012 ACCF/AHA/HRS focused update incorporated into the ACCF/AHA/HRS 2008 guidelines for device-based therapy of cardiac rhythm abnormalities: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines and the Heart Rhythm Society.2012年美国心脏病学会基金会/美国心脏协会/心律学会重点更新内容纳入《2008年美国心脏病学会基金会/美国心脏协会/心律学会心脏节律异常器械治疗指南》:美国心脏病学会基金会/美国心脏协会实践指南工作组及心律学会报告
J Am Coll Cardiol. 2013 Jan 22;61(3):e6-75. doi: 10.1016/j.jacc.2012.11.007. Epub 2012 Dec 19.
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Apical hypertrophic cardiomyopathy with apical aneurysm in an African-American male.一名非裔美国男性患伴有心尖部动脉瘤的肥厚型心肌病。
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