两名尼日利亚成年男性的害羞-Drager综合症

C. A. Ukoh
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摘要

压力感受器敏感性随年龄增长和全身性高血压而降低。因此,血液循环对体位变化的快速调节可能会受损,从而发生体位性低血压。其中一个很好的例子就是希-德尔格综合征,多系统萎缩伴自主神经衰竭,以体位性低血压为特征。虽然是一种罕见的疾病,但由于诊断和治疗的困难,美国国家神经疾病和中风研究所(NINDS)最近对它产生了很大的兴趣。虽然相关病例比比皆是,但在尼日利亚文献中尚未报道典型的施德综合征病例。以下是两名尼日利亚成年男子的病例报告。第一个病例是一名70岁的比尼族男子,已知患有高血压,因良性前列腺肥大(BPH)、麻痹和偶尔的定向障碍而接受治疗。后来,他被诊断为希-德格综合症。第二个病例是一名52岁的比尼族男子,因反复晕厥发作而丧失行为能力。两人均对醋酸氢化可的松治疗反应良好。这在我们的环境中是非常罕见的。关键词:施德氏综合征;尼日利亚,男性,成人。生物医学科学年鉴Vol. 2 (1) 2003: pp. 54-58
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Shy –Drager Syndrome In Two Nigerian Male Adults
Baroreceptor sensitivity decreases with advancing age and systemic hypertension. In consequence, rapid adjustment of the circulation to changes in posture may be impaired so that postural hypotension occurs. One such condition where this is well demonstrated is the Shy-Drager Syndrome, multiple system atrophy with autonomic failure characterized by postural hypotension. Though a rare disease, a lot of interest has recently been focused on it by the National Institute of Neurological Disease and Stroke (NINDS) because of difficulties in diagnosis and treatment. Typical cases of Shy-Drager Syndrome have not been reported in the Nigerian literature although related cases abound. The following are case reports of two adult Nigerian males. The first is that of a 70-year-old Bini man, a known hypertensive who was being managed for benign prostatic hypertrophy (BPH), parapareisis and occasional disorientation. He was later diagnosed as a case of Shy-Drager Syndrome. The second is that of a 52-year-old Bini man who became incapacitated by recurrent syncopal attacks. Both responded well to treatment with fludrocortisone acetate. A very rare condition in our environment. The need for its awareness is hereby emphasized Keywords : Shy-Drager Syndrome; Nigerian, Male, Adult. Annals of Biomedical Science Vol. 2 (1) 2003: pp. 54-58
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