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Pheochromocytoma as a rare cause of hypertension in a 46 X i(X)(q10) turner syndrome: a case report and literature review

机译:嗜铬细胞瘤是46 Xi(X)(q10)特纳综合征中高血压的罕见原因:一例病例报告和文献复习

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摘要

BackgroundCardiovascular disease (CVD) presents the most serious health problems and contributes to the increased mortality in young women with Turner syndrome. Arterial hypertension in Turner syndrome patients is significantly more prevalent than that in a general age-matched control group. The aetiology of hypertension in Turner syndrome varies, even in the absence of cardiac anomalies and obvious structural renal abnormalities. Pheochromocytoma is an extremely rare cause among various etiologies for hypertension in patients with Turner syndrome. Here, we reported a pheochromocytoma as a rare cause of hypertension in Turner syndrome patient.
机译:背景技术心血管疾病(CVD)带来了最严重的健康问题,并导致特纳综合征的年轻女性死亡率增加。 Turner综合征患者的动脉高血压明显比一般年龄匹配的对照组更为普遍。即使没有心脏异常和明显的肾脏结构异常,Turner综合征的高血压病因也有所不同。嗜铬细胞瘤是特纳综合征患者各种高血压病中极为罕见的原因。在这里,我们报道了嗜铬细胞瘤是特纳综合征患者高血压的罕见原因。

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