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小儿Mulibrey纳米病中的心包缩窄和心肌受限:一种伴有舒张功能障碍的复杂疾病

Pericardial Constriction and Myocardial Restriction in Pediatric Mulibrey Nanism: A Complex Disease With Diastolic Dysfunction.

作者信息

Sarkola Taisto, Lipsanen-Nyman Marita, Jalanko Hannu, Jokinen Eero

机构信息

Division of Cardiology, Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Minerva Foundation Institute for Medical Research, Helsinki, Finland.

出版信息

CJC Open. 2021 Aug 30;4(1):28-36. doi: 10.1016/j.cjco.2021.08.012. eCollection 2022 Jan.

Abstract

BACKGROUND

Mulibrey nanism (MUL) is a rare condition with profound growth delay. Congestive heart failure is a major determinant of prognosis. The aim was to delineate pericardial constriction and myocardial functional abnormalities in a pediatric MUL sample.

METHODS

A total of 23 MUL patients and 23 individually sex- and age-matched healthy control subjects were prospectively assessed in a cross-sectional study with echocardiography.

RESULTS

Clinical signs of heart failure were present in 7 MUL patients, with severe congestive heart failure in 2. Significant diastolic dysfunction, mainly related to constriction, was found in MUL patients without pericardiectomy (N = 18)-septal bounce, pronounced hepatic vein atrial reversal and right heart inflow-outflow variations, and decreased inferior vena cava collapse during respiration. The appearance of the pericardium was not different from that of control subjects. Longitudinal diastolic myocardial velocities were similar to those in control subjects, suggesting an absence of significant myocardial restriction. Right ventricular free wall longitudinal systolic strain and bilateral longitudinal myocardial systolic velocities were decreased in MUL patients, indicating mild biventricular systolic dysfunction. Myocardial motion abnormalities and persistent congestive heart failure were common (in 3 of 6) in MUL patients with a history of pericardiectomy. Cardiac dimensions were similar between MUL patients and control subjects when adjusting for body size, except for smaller biventricular volumes.

CONCLUSIONS

MUL disease presents with significant constriction-related diastolic dysfunction and mild bilateral systolic dysfunction. Constriction-restriction assessments during follow-up could be of benefit in decision-making regarding pericardiectomy in MUL disease. Myocardial abnormalities were prevalent among MUL patients who had undergone pericardiectomy and are consistent with progression of myocardial disease in a significant proportion of patients.

摘要

背景

穆利布雷侏儒症(MUL)是一种罕见的伴有严重生长发育迟缓的疾病。充血性心力衰竭是预后的主要决定因素。目的是在儿科MUL样本中明确心包缩窄和心肌功能异常情况。

方法

在一项采用超声心动图的横断面研究中,对23例MUL患者和23例性别及年龄匹配的健康对照者进行了前瞻性评估。

结果

7例MUL患者出现心力衰竭临床体征,其中2例为严重充血性心力衰竭。在未行心包切除术的MUL患者(N = 18)中发现明显的舒张功能障碍,主要与缩窄有关——室间隔跳动、明显的肝静脉心房反流及右心流入流出变化,以及呼吸时下腔静脉塌陷减少。心包外观与对照者无异。纵向舒张期心肌速度与对照者相似,提示无明显心肌受限。MUL患者右心室游离壁纵向收缩期应变及双侧纵向心肌收缩速度降低,表明存在轻度双心室收缩功能障碍。有过心包切除术病史的MUL患者中,心肌运动异常和持续性充血性心力衰竭很常见(6例中有3例)。调整体型后,MUL患者与对照者的心脏尺寸相似,但双心室容积较小。

结论

MUL病表现为与缩窄相关的明显舒张功能障碍和轻度双侧收缩功能障碍。随访期间进行缩窄 - 受限评估可能有助于MUL病心包切除术的决策制定。心肌异常在接受心包切除术的MUL患者中普遍存在,且在相当比例的患者中与心肌疾病进展一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5a3/8767125/71bde42a5480/gr1.jpg

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