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左心室心肌致密化不全:14例病例的病理学研究

Left ventricular noncompaction: a pathological study of 14 cases.

作者信息

Burke Allen, Mont Erik, Kutys Robert, Virmani Renu

机构信息

Department of Cardiovasular Pathology, Armed Forces Institute of Pathology, Washington, DC 20306, USA.

出版信息

Hum Pathol. 2005 Apr;36(4):403-11. doi: 10.1016/j.humpath.2005.02.004.

Abstract

Left ventricular noncompaction (LVNC) has been recently proposed as a specific form of cardiomyopathy. There have been few pathological series describing gross and microscopic findings of this entity, especially in children. We present findings of 14 hearts (13 autopsy and 1 explant) with LVNC (isolated and associated with congenital heart disease), defined by poorly developed left ventricular (LV) papillary muscles and a noncompact inner LV myocardial layer comprising more than 50% of the LV thickness. The mean age at death/explant was 3.6 years (median, 2.5 months); there were 6 boys and 8 girls. The symptoms were sudden unexpected death (10) and heart failure (4). The diagnosis was suspected before death in only 1 of 13 autopsy cases. Right ventricular involvement (> 75% ventricular thickness comprised of noncompacted area with recess adjacent to tricuspid valve) was seen in 6 of 14 hearts. One patient had a sibling with pulmonary stenosis, but there was no other known familial cardiomyopathy. Endocardial fibroelastosis was a characteristic histological feature, as well as anastomosing or polypoid endocardial trabeculations, which resulted in staghorn-shaped, endocardial-lined recesses. There was a high rate of other cardiac anomalies, which often coexisted and were not clearly related to the LVNC, present in 8 cases (nonisolated LVNC): ventricular septal defect (4/14), anomalous venous pulmonary veins (1/14), coronary ostial stenosis (1/14), histiocytoid cardiomyopathy (1/14), polyvalvar dysplasia (2/14), and pulmonary stenosis (2/14). In the 6 isolated LVNC, there were 2 malformed atrioventricular valves (1 mitral and 1 tricuspid), which appeared part of the ventricular maldevelopment. There were no differences in histological or gross patterns of the noncompacted regions between the isolated and nonisolated LVNC. LVNC is frequently associated with other cardiac defects, especially when causing sudden death in infants and children. A clear-cut morphological distinction between "isolated" and "secondary" LVNC was not apparent. The pathologist should be aware of the entity because the diagnosis is often first established at autopsy.

摘要

左心室心肌致密化不全(LVNC)最近被认为是一种特殊形式的心肌病。描述该实体大体和微观表现的病理系列报道很少,尤其是在儿童中。我们展示了14例患有LVNC(孤立性及合并先天性心脏病)心脏的研究结果(13例尸检和1例心脏外植体),其定义为左心室(LV)乳头肌发育不良,且左心室内层心肌致密化不全层厚度超过左心室厚度的50%。死亡/心脏外植体时的平均年龄为3.6岁(中位数为2.5个月);其中6例为男孩,8例为女孩。症状包括猝死(10例)和心力衰竭(4例)。13例尸检病例中仅有1例在死亡前被怀疑患有该病。14例心脏中有6例可见右心室受累(超过75%的心室厚度由紧邻三尖瓣的致密化不全区域组成)。1例患者有1名患肺动脉狭窄的同胞,但无其他已知的家族性心肌病。心内膜弹力纤维增生症是一种特征性组织学表现,还有吻合状或息肉状心内膜小梁,形成鹿角状、内衬心内膜的隐窝。其他心脏异常发生率很高,常并存且与LVNC无明显关联,8例(非孤立性LVNC)存在:室间隔缺损(4/14)、肺静脉异位引流(1/14)、冠状动脉开口狭窄(1/14)、组织细胞样心肌病(1/14)、多瓣膜发育异常(2/14)和肺动脉狭窄(2/14)。在6例孤立性LVNC中,有2例房室瓣畸形(1例二尖瓣和1例三尖瓣),似乎是心室发育异常的一部分。孤立性和非孤立性LVNC的致密化不全区域在组织学或大体形态上无差异。LVNC常与其他心脏缺陷相关联,尤其是在导致婴幼儿猝死时。“孤立性”和“继发性”LVNC之间没有明显的形态学区别。病理学家应了解该实体,因为诊断通常首先在尸检时确立。

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