特发性脊柱侧凸患者猝死1例

Fumiko Satoh (MD, PhD) , Masaki Q. Fujita (MD, PhD) , Yoshihisa Seto , Akio Tsuboi , Sanae Takeichi (MD, PhD)
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引用次数: 3

摘要

我们报告一个尸检病例猝死在一个36岁的工匠特发性脊柱侧凸。医生在他13岁时确诊了他的脊柱侧弯,他接受了三年的医疗护理,直到他不再看医生。他在车站行走时晕倒,在心肺骤停状态下被送往急诊室,尽管进行了一个多小时的心肺复苏术,但仍被宣布死亡。双侧眼睑结膜可见大量瘀点,嘴唇呈紫绀。除了在脸上观察到的小擦伤外,没有特别的伤害。背部因胸中侧凸(Cobb角73°)显示右肋隆起,右半胸变形,前方显示漏斗胸外观。右胸腔容积明显减小。右肺间质纤维化广泛,肺泡结构几乎未见正常,肺小动脉壁内侧肥大。由于这些肺部改变导致的右心室肥厚和其他器官充血,表明本病例的死亡原因是肺动脉高压引起的肺心病。这是一个罕见的病例致命的结果,晚期特发性脊柱侧凸没有医疗护理,尽管早期发现通过大规模筛查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sudden death in a patient with idiopathic scoliosis

We report an autopsy case of sudden death in a 36-year-old craftsman with idiopathic scoliosis. The doctor identified his scoliosis at the age of thirteen, and he was under medical care for three years until he stopped consulting the doctor. He collapsed while walking at the station and was sent to an emergency room in cardiopulmonary arrest state, where he was declared dead in spite of more than an hour of CPR. Numbers of petechiae were seen on the bilateral palpebral conjunctivae and the lips were cyanotic. There were no particular injuries except for small abrasions observed on the face. The back showed right rib hump owing to midthoracic scoliosis (with 73° of Cobb’s angle) and right hemithorax was deformed showing an appearance of pectus excavatum in the front. The volume of the right thoracic cavity was significantly decreased. In the right lung, there was extensive stromal fibrosis, leaving almost no normal alveolar structures, and medial hypertrophy of pulmonary arteriolar walls. Hypertrophy of the right heart ventricle due to these pulmonary changes and the congestion of other organs suggested that the cause of death in this case was cor pulmonale due to pulmonary hypertension. This was a rare case of fatal outcome of advanced idiopathic scoliosis without medical care in spite of early detection through mass screening.

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