HYPERTENSION IN CASES OF CONGENITAL POLYCYSTIC KIDNEY
HYPERTENSION IN CASES OF CONGENITAL POLYCYSTIC KIDNEY
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先天性多囊肾病例中的高血压
DOI：
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发表时间：
1931
期刊：
影响因子：
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通讯作者：
F. W. Schacht
中科院分区：
文献类型：
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作者：
F. W. Schacht
先天性多囊肾患者是否存在持续性高血压一直是文献中的争议点。许多研究者1已经引起了人们对与这种情况相关的高血压发病率的关注。1928年，Bell和Clawson在回顾了文献和对8个病例的研究后得出结论：“现有的信息强烈反对先天性肾脏囊性疾病伴有持续性高血压的观点。1914年，Veil 3研究了三个在临床检查中确诊为多囊肾的病例。患者为女性，年龄在42至50岁之间。在每种情况下，心脏都没有扩大，但血压升高。Veil坚持认为，没有心脏肥大是对持续性高血压的反对，因为没有明显的肾功能不全，他不认为高血压可能是肾源性的。中
The presence of persistent hypertension in cases of congenital polycystic kidney has been a disputed point in the literature. Various investigators 1 have called attention to the high incidence of hypertension associated with this condition. In 1928, Bell and Clawson, 2 after a review of the literature and a study of eight cases, concluded: "The available information is strongly against the view that congenital cystic disease of the kidneys is accompanied by persistent hypertension." In 1914, Veil 3 studied three cases in which a definite diagnosis of polycystic kidney had been made at a clinical examination. The patients were women, aged between 42 and 50. In each case the heart was not enlarged, but the blood pressure was elevated. Veil maintained that the absence of cardiac hypertrophy was against persistent hypertension, and because there was not marked renal insufficiency, he did not think that the hypertension could be of renal origin. In a