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首页> 外文期刊>The American Journal of the Medical Sciences >Idiopathic intracranial hypertension associated with either primary or secondary aldosteronism
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Idiopathic intracranial hypertension associated with either primary or secondary aldosteronism

机译:特发性颅内高压伴原发性或继发性醛固酮增多症

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摘要

BACKGROUND:: Idiopathic intracranial hypertension (IIH) is a syndrome consisting of headache, visual field defects and papilledema of uncertain etiology. The prospect was raised previously as to an association between aldosteronism and increased intracranial pressure in 2 middle-aged women with IIH and primary aldosteronism (PAL). Since then, 2 additional adults were identified and 2 other cases were reported from the United Kingdom, whereas 6 cases of IIH and secondary aldosteronism (SAL) in children have been reported in the English literature worldwide. METHODS:: A retrospective analysis of cases from author institutions and published literature comparing clinical features, laboratory findings and therapeutic interventions in these 12 cases. RESULTS:: The female-to-male ratio was 10:2. The mean age of the PAL patients was 49 ± 3 years - all hypertensive, with adrenal pathology in most. The mean age of the SAL patients was 11 ± 2 years - mostly normotensive, with 3 having Bartters and 2 Gitelman syndromes, and 1 renal congenital hypoplasia. Plasma aldosterone levels were elevated (31 ± 5 ng/dL) in PAL and SAL, whereas plasma renin activity was suppressed in PAL. Hypokalemia (3.2 ± 0.2 mmol/L), hypomagnesemia (1.6 ± 0.3 mg/dL) and a putative metabolic alkalosis (serum HCO3 30 ± 1 mmol/L) were observed. IIH symptoms were controlled by spironolactone in 5, amiloride in 1, correction of hypokalemia and hypomagnesemia in 2, discontinuation of nonsteroidal anti-inflammatory drugs in 2, and reduction of body weight in 1. One patient required serial lumbar punctures, 2 a ventriculoperitoneal shunt, whereas all 3 patients with adrenal adenoma underwent surgical resection. CONCLUSIONS:: An association between IIH and PAL occurs in hypertensive middle-aged women, whereas normotensive girls having an inherited renal tubular defect may have IIH with SAL. Patients with IIH should be evaluated for aldosteronism and considered for spironolactone therapy.
机译:背景:特发性颅内高压症(IIH)是一种由头痛,视野缺损和病因不明的乳头状水肿组成的综合征。先前有关醛固酮增多症与2例IIH和原发性醛固酮增多症(PAL)的中年妇女颅内压升高之间的关联的前景被提出。从那时起,英国又发现了另外2名成年人,另外2例是英国报告的,而全世界英语文献中都报告了6例IIH和儿童继发性醛固酮增多症(SAL)。方法:对来自作者机构和已发表文献的病例进行回顾性分析,比较这12例病例的临床特征,实验室检查结果和治疗干预措施。结果::男女比例为10:2。 PAL患者的平均年龄为49±3岁-全部为高血压,大多数为肾上腺病理。 SAL患者的平均年龄为11±2岁-多数为血压正常,其中3例患有Bartters综合征和2例Gitelman综合征,以及1例先天性肾发育不全。 PAL和SAL中血浆醛固酮水平升高(31±5 ng / dL),而PAL中血浆肾素活性受到抑制。低钾血症(3.2±0.2 mmol / L),低镁血症(1.6±0.3 mg / dL)和假定的代谢性碱中毒(血清HCO3 30±1 mmol / L)被观察到。 IIH症状由螺内酯5,阿米洛利1,纠正低血钾和低镁血症2,停用非甾体类抗炎药2,减轻体重1来控制。一名患者需要连续腰穿,2进行腹膜-腹膜分流,而所有3例肾上腺腺瘤患者均接受了手术切除。结论:IIH和PAL之间的关联发生在高血压的中年妇女中,而具有遗传性肾小管缺陷的血压正常的女孩可能与SAL发生IIH。 IIH患者应评估醛固酮增多症,并考虑使用螺内酯治疗。

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