Isolated right ventricular noncompaction in an adult woman with severe pulmonary hypertension following at the intensive care unit

M. Yıldız, Yasemin Ozsahin, H. Yılmaz Ak, D. Oksen
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Abstract

Pulmonary hypertension is defined by a mean pulmonary artery pressure ≥25 mmHg at rest, measured during right heart catheterization. Ventricular noncompaction is a genetic cardiomyopathy which mostly effects left ventricle. It is related with deterioration of myocardial embryogenesis and commonly together with other cardiac diseases (1). Isolated ventricular non-compaction is characterized by modified morphology of myocardial wall, increased trabeculation in ventricular cavity and deep intertrabecular recesses. A 43-year-old woman presented exercise induced dyspnea and atypical chest pain. She has not any medical history prior. On admission, her 12 lead ECG showed complete righ bundle branch block, her blood pressure was 120/80 and pulse rate 80 per minutes. Transthoracic 2D echocardiogram and magnetic resonance imaging showed dilated and hypertrophied right ventricle with non-compaction of the right ventricular apex. The systolic pulmonary arterial pressure was 80 mmHg on the Doppler echocardiography. The coronary angiography revealed normal coronary arteries. The catheterization was showed pulmonary hypertension, right ventricle non-compaction and negative pulmonary vasoreactivity testing. Ventricular noncompaction, especially right ventricular noncompaction, complicated by severe pulmonary hypertension is exceptional. Only a few isolated right ventricular noncompaction has been reported but inclusion of pulmonary hypertesion cases are rare subsets . Diagnosis of pulmonary hypertension may be a consequence of increased pulmonary venous pressures caused by systolic and diastolic ventricular dysfunction secondary to right ventricular noncompaction. Widespread usage of cardiac magnetic resonance imaging, may enhance visual quality and evaluation of ventricular morphology, probably this will provide prevalance increment and clinical outcome improvements. Early diagnosis would bring better results.
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孤立的右心室不压实在一个成年妇女与严重肺动脉高压后,在重症监护病房
肺动脉高压的定义是静息时平均肺动脉压≥25 mmHg,在右心导管插入术中测量。心室非压实性心肌病是一种主要影响左心室的遗传性心肌病。它与心肌胚胎发生的恶化有关,并常与其他心脏疾病一起发生(1)。孤立性心室不压实的特征是心肌壁形态改变,室腔小梁增加,小梁间凹陷深。一位43岁的女性表现为运动引起的呼吸困难和非典型胸痛。她之前没有任何病史。入院时,12导联心电图显示右束支完全阻滞,血压120/80,脉率80 /分钟。经胸二维超声心动图和磁共振成像显示右心室扩张和肥厚,右心室心尖不致密。多普勒超声心动图显示肺动脉收缩压80 mmHg。冠状动脉造影显示冠状动脉正常。导管检查显示肺动脉高压,右心室不压实,肺血管反应性阴性。心室压实不全,尤其是右心室压实不全,合并严重肺动脉高压是罕见的。只有少数孤立的右心室不压实已被报道,但包括肺动脉高压病例是罕见的亚群。肺动脉高压的诊断可能是继发于右心室不压实的收缩期和舒张期心室功能障碍引起的肺静脉压力升高的结果。心脏磁共振成像的广泛应用,可能会提高视觉质量和心室形态学的评估,这可能会提供患病率的增加和临床结果的改善。早期诊断会带来更好的结果。
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