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异构综合征中心房形态和窦房结形态的特征:基于 41 例尸检(1950-2008 年)的研究。

Characterization of atrial morphology and sinus node morphology in heterotaxy syndrome: an autopsy-based study of 41 cases (1950-2008).

机构信息

Mayo Medical School, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Cardiovasc Pathol. 2012 Sep-Oct;21(5):421-7. doi: 10.1016/j.carpath.2011.12.007. Epub 2012 Jan 28.

Abstract

BACKGROUND

Heterotaxy syndrome affects the sidedness of heart, lungs, and abdominal viscera, and is associated with complex congenital heart disease. Cardiac sidedness is defined by the position of the morphological right atrium and may be normal, mirror-image, or isomeric. The sinus node has been reported to be present bilaterally in right isomerism and absent bilaterally in left isomerism, although exceptions may occur.

OBJECTIVE

Our aim was to evaluate bilaterally the presence or absence of sinus node tissue in autopsy-derived hearts from patients with heterotaxy and to correlate the findings with the sidedness of the two atria.

METHODS

Autopsy and clinical records were reviewed from 41 cases with heterotaxy. From the cardiac specimens, tissue was collected bilaterally from expected sinus node sites. Sinus node tissue was categorized microscopically as normal, hypoplastic, indeterminate, or absent.

RESULTS

In hearts thought to show right atrial isomerism, sinus node tissue was detected bilaterally in 54%, was absent on one side in 43%, and was absent on both sides in 3%. For cases with apparent left atrial isomerism, a single sinus node was present in the left-sided atrium in 75% of cases and was absent bilaterally in 25%.

CONCLUSIONS

Bilateral sinus nodes were observed in only 54% of cases with right isomerism, and bilateral absence of sinus nodes was documented in only 25% of cases with left isomerism. Thus, our findings indicate that the sinus node is not a morphologically right-sided structure, and its presence therefore is not consistently related to the sidedness of the atria.

摘要

背景

异构综合征会影响心脏、肺部和腹部内脏的偏侧性,并与复杂的先天性心脏病有关。心脏偏侧性由形态右心房的位置定义,可能正常、镜像或同型。尽管可能存在例外情况,但据报道,右同型性中双测存在窦房结,而左同型性中双侧窦房结缺失。

目的

我们旨在评估异构患者尸检心脏中窦房结组织是否双侧存在,并将发现与两心房的偏侧性相关联。

方法

对 41 例异构患者的尸检和临床记录进行了回顾。从心脏标本中,双侧采集预期窦房结部位的组织。窦房结组织通过显微镜分类为正常、发育不良、不确定或缺失。

结果

在被认为表现为右心房同型性的心脏中,窦房结组织双侧存在的比例为 54%,单侧缺失的比例为 43%,双侧缺失的比例为 3%。对于明显的左心房同型性,75%的病例左侧心房有单个窦房结,25%的病例双侧窦房结缺失。

结论

只有 54%的右同型性病例观察到双侧窦房结,只有 25%的左同型性病例记录到双侧窦房结缺失。因此,我们的发现表明窦房结不是形态上的右侧结构,其存在因此与心房的偏侧性不一致。

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