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首页> 外文期刊>Pediatrics: Official Publication of the American Academy of Pediatrics >AN AMERICAN CASE REPORT OF APPARENT TETRALOGY OF FALLOT PUBLISHED ALMOST FIFTY YEARS PRIOR TO FALLOT'S CLASSIC REPORT IN 1888
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AN AMERICAN CASE REPORT OF APPARENT TETRALOGY OF FALLOT PUBLISHED ALMOST FIFTY YEARS PRIOR TO FALLOT'S CLASSIC REPORT IN 1888

机译:在1888年Fallot的经典报告发表之前,Fallot发表了近五十年的明显四面体的美国案例报告

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In 1888 Etienne L. A. Fallot (1850-1911) gave an important but not the first account of the condition that bears his name.1 The earliest American description of a child with putative tetralogy of Fallot that I have been able to find was reported in 1842 as follows:About two years since, I was called to visit a child of Mr. S., of this town, aged two years and six months. Mrs. S. related the history of the case as follows. From birth to the age of eleven months, there was nothing unnatural in the health or appearance of the child. At this time it began to be very much afflicted by ill turns, attended with laborious respiration, palpitation and a peculiar blueness of the skin. After a few minutes the paroxysm would pass off, leaving her in a state of great exhaustion. These paroxysms continued, at regular intervals, with increasing severity, up to the time of its death, which occurred on the 14th inst.Post-mortem Examination, Sixteen Hours after Death. —Body very much emaciated; face bloated; skin blue; lungs small and dark colored; one and a half ounces of serum in pericardium; heart weighed five and a half ounces; hypertrophy of right ventricle; aorta communicated with both ventricles equally; pulmonary artery very small; its communication with the right ventricle would barely admit a common blunt-pointed probe; foramen ovate imperfectly closed. The remaining viscera natural, with the exception of color, which might be expected from the imperfect arterialization of the blood ( A. C. Smith, MD, Haverhill [ MA ], July 22, 1842 ).
机译:1888年,艾蒂安·法洛(Etienne LA Fallot,1850-1911年)给出了重要但并非首次的关于以他的名字命名的疾病的说明。1据报道,我在1842年发现了美国最早的关于法洛特四联症儿童的描述。如下所示:大约两年后,我被叫去看望这个镇上S.先生的孩子,年龄为2年零6个月。 S太太将案件的历史叙述如下。从出生到十一个月大,孩子的健康或外表没有异常。在这个时候,它开始非常受不舒服的折磨的困扰,伴随着费力的呼吸,心慌和皮肤特有的发蓝。几分钟后,发作会消失,使她处于精疲力竭的状态。这些发作持续到死后16个小时,以定期的间隔不断增加,直至死亡为止。身体非常瘦弱;脸肿了皮肤发蓝;肺小而深色;心包中有半盎司的血清;心脏重达五个半盎司;右心室肥大;主动脉与两个心室平均连通;肺动脉很小;它与右心室的交流几乎不能接受一个普通的钝头探针。卵圆孔不完全闭合。剩余的内脏是自然的,但颜色除外,这可能是由于血液的不完全动脉化所预期的(A. C. Smith,医学博士,Haverhill [MA],1842年7月22日)。

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