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摘要:
The X-linked adrenoleukodystrophy (ALD) is a severe neurodegenerative disorder due to mutations in the ABCD1 gene. Objective: To report a case of a 19-year-old man with adrenal insufficiency due to adrenoleukodystrophy. Method: Case report and literature review. Result: A previously healthy 19-year-old male patient was admitted to the emergency room with nausea and vomiting for 5 days, who progressed to abdominal pain, severe asthenia, and fever (38.5°C). He referred progressive darkening of the skin, oral mucosa, tongue and nail bed of the hands and feet, observed in the last 6 years. Emergency laboratory evaluation showed severe hyponatremia and hyperkalemia, which, together with decreased plasma cortisol, directed the investigation to causes of adrenal insufficiency. High ACTH (Adrenocorticotropic hormone) and very long chain fatty acid levels closed the diagnosis. Discussion: ALD is characterized by progressive demyelination in the central and peripheral nervous system and adrenal insufficiency consequence to the accumulation of very long chain fatty acids (VLCFA) in the adrenal. The overall incidence of ALD is 1:17,000. Adrenal insufficiency may be the first symptom of ALD in boys and adults. The diagnosis is based on the measurement of VLCFA plasma levels. Allogeneic bone marrow transplantation is the only treatment that provides a permanent cure when the procedure is performed at an early stage of brain demyelination, i.e. when patients are asymptomatic, although brain magnetic resonance imaging (MRI) is abnormal. Treatment of Addison’s disease is obligatory, but does not change the course of neurological symptoms.
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篇名 Adrenal Insufficiency by Adrenoleukodystrophy
来源期刊 健康(英文) 学科 医学
关键词 ADRENOLEUKODYSTROPHY ADRENOMYELONEUROPATHY ADRENAL INSUFFICIENCY Addison’s DISEASE
年,卷(期) 2020,(1) 所属期刊栏目
研究方向 页码范围 1-13
页数 13页 分类号 R57
字数 语种
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研究主题发展历程
节点文献
ADRENOLEUKODYSTROPHY
ADRENOMYELONEUROPATHY
ADRENAL
INSUFFICIENCY
Addison’s
DISEASE
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期刊影响力
健康(英文)
月刊
1949-4998
武汉市江夏区汤逊湖北路38号光谷总部空间
出版文献量(篇)
328
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0
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0
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