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肥厚型心肌病与年轻人猝死:心肌缺血的病理证据

Hypertrophic cardiomyopathy and sudden death in the young: pathologic evidence of myocardial ischemia.

作者信息

Basso C, Thiene G, Corrado D, Buja G, Melacini P, Nava A

机构信息

Department of Pathology, University of Padua Medical School, Italy.

出版信息

Hum Pathol. 2000 Aug;31(8):988-98. doi: 10.1053/hupa.2000.16659.

Abstract

The mechanism underlying cardiac arrest in patients with hypertrophic cardiomyopathy (HC) is intriguing. In the clinical setting, myocardial ischemia has long been incriminated, particularly in the young. Among 274 cardiovascular sudden deaths in the young (< or = 35 years), 19 (7.0%), 14 males and 5 females, median age 23 years, had HC. Familial occurrence of HC was ascertained in 3 (16%). SD occurred on effort in 6 (31%). Previous syncope occurred in 5 and palpitations in 3. Basal electrocardiogram (ECG) was abnormal in 7 of 8 available cases. Hypertrophy was septal asymmetric in 14. Gross examination showed large isolated or multiple septal scars in 11 (58%); at histomorphometry, the mean percent area of fibrosis of the septal myocardium was 18.6 +/- 6. Four showed a deep intramyocardial course of the left anterior descending coronary artery. At histology, myocardial disarray involved 30 +/- 16% of the septal myocardium; evidence of acute-subacute myocardial necrosis was present in 14 (74%), 1 of them with a regional acute myocardial infarction. By comparing hearts with (n = 11) and without (n = 8) areas of scar-type fibrosis, we found a statistically significant difference in terms of age (25.5 +/- 5.4 v 15.5 +/- 12.4 years, P = .04), septal thickness (25.4 +/- 5.4 v 15.4 +/- 4.9 mm, P < .001), percent increase of septal thickness versus normal value for age and sex (46.2 +/- 15 v 25.2 +/- 13.6%, P < .01) and mean score of small vessel disease (1.7 +/- 0.4 v 1.2 +/- 0.4, P = .04). Linear regression analysis showed a positive correlation of percent area of replacement fibrosis with septal thickness (P = .01) and with mean score of small vessel disease (P < .01). In conclusion, our pathologic findings of ischemic damage, either acute-subacute or in the form of fibrotic scars, support the clinical evidence that ischemia occurs in the natural history of HC and may contribute to life-threatening electrical instability.

摘要

肥厚型心肌病(HC)患者心脏骤停的潜在机制很有趣。在临床环境中,心肌缺血长期以来一直被认为是原因之一,尤其是在年轻人中。在274例年轻(≤35岁)心血管性猝死病例中,19例(7.0%)患有HC,其中男性14例,女性5例,中位年龄23岁。3例(16%)有HC家族史。6例(31%)猝死发生在运动时。5例曾有晕厥,3例有心悸。8例可获取的病例中,7例基础心电图(ECG)异常。14例为不对称性室间隔肥厚。大体检查显示,11例(58%)有单个或多个较大的室间隔瘢痕;组织形态计量学显示,室间隔心肌纤维化的平均面积百分比为18.6±6。4例显示左前降支冠状动脉走行于心肌深层。组织学检查显示,心肌排列紊乱累及30±16%的室间隔心肌;14例(74%)有急性-亚急性心肌坏死证据,其中1例有区域性急性心肌梗死。通过比较有(n = 11)和无(n = 8)瘢痕型纤维化区域的心脏,我们发现年龄(25.5±5.4对15.5±12.4岁,P = 0.04)、室间隔厚度(25.4±5.4对15.4±4.9mm,P < 0.001)、室间隔厚度相对于年龄和性别的正常值增加百分比(46.2±15对25.2±13.6%,P < 0.01)以及小血管疾病平均评分(1.7±0.4对1.2±0.4,P = 0.04)方面存在统计学显著差异。线性回归分析显示,替代纤维化面积百分比与室间隔厚度(P = 0.01)和小血管疾病平均评分(P < 0.01)呈正相关。总之,我们关于急性-亚急性缺血性损伤或纤维化瘢痕形式的病理学发现,支持了临床证据,即缺血发生在HC的自然病程中,并可能导致危及生命的电不稳定。

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