柏金遜綜合症
柏金遜綜合症(Parkinsonism)是和運動機能相關的臨床綜合症,其特徵是顫抖、運動功能減退、僵硬及平衡障礙[1][2]。在柏金遜氏症(PD)患者身上會有類似徵狀(此綜合症因此而得名),而路易氏體認知障礙症(DLB)、柏金遜症性認知障礙症(PDD)等疾病也會有此徵狀。這類綜合症的病因範圍很廣,包括神經退化障礙疾病、藥物、毒素、代謝疾病,或是柏金遜氏症以外的神經性疾病[3]。
柏金遜綜合症 Parkinsonism | |
---|---|
病因 | |
分類和外部資源 | |
醫學專科 | 神經學 |
ICD-11 | 8A00 |
ICD-10 | G21、G22 |
DiseasesDB | 24212 |
MedlinePlus | 000759 |
Orphanet | 68402 |
病因
藥物引起
有柏金遜綜合症的人當中,約有7%是因為藥物的副作用而造成的,主要是因為抗精神病藥,特別是吩噻嗪(例如perphenazine及氯丙嗪)、噻噸(例如三氟噻噸及珠氯噻醇)及丁酰苯(例如氟哌啶醇),偶爾也有因為抗憂鬱藥物而造成。藥物引起柏金遜綜合症的盛行率會隨年齡而上昇。藥物引起的柏金遜綜合症一但出現,多半會維持原有的程度,不像柏金遜氏症會漸漸惡化[4]。
毒素
有發現殺蟲劑或除草劑暴露程度和柏金遜氏症之間的關聯性。若暴露在百草枯或錳乃浦/鋅錳乃浦下,風險是原來的兩倍[5]。
已證實慢性錳(Mn)暴露會造成類似柏金遜綜合症的疾病,其特徵是運動障礙,此徵狀無法用典型的柏金遜症治療方式來治療,因此推測除了典型黑質內多巴胺能損失外,包括有其他的致病途徑[6]。錳會在基底核內累積,因此造成運動障礙[7]有一種和SLC30A10基因(錳外流轉運蛋白,減少細胞內錳所必需的蛋白)有關的變異和這種類似柏金遜綜合症疾病有關[8]。在這疾病中看不到柏金遜氏症中典型的路易體[7]。
診斷
許多疾病會造成柏金遜綜合症。
- 皮質基底核退化症[9]
- 路易氏體認知障礙症[9]
- 額顳認知障礙症(匹克氏病)[10]
- 格斯特曼–斯特勞斯勒–申克綜合症[9]
- 亨丁頓舞蹈症[9]
- Lytico-bodig症(ALS complex of Guam)[9]
- 多系統萎縮(Shy–Drager綜合症)[9]
- 神經吞噬作用[9]
- 神經元蠟樣脂褐質儲積症[9]
- 少腦橋小腦萎縮[9]
- 泛酸鹽激活酵素關聯之神經退化性疾病,也稱為具有腦部鐵質積聚的神經變性(neurodegeneration with brain iron accumulation)[9]
- 帕金突變(遺傳性青少年肌張力障礙)[9]
- 柏金遜氏症[9]
- 柏金遜氏症性認知障礙症[11]
- 進行性上眼神經核麻痺症[9]
- 肝豆狀核變性[9]
- X連鎖性肌張力障礙柏金遜症(Lubag綜合症)[9]
- 藥物引發(偽柏金遜綜合症)
- 感染
- 毒素
- 番荔枝科[16]
- 一氧化碳[9]
- 二硫化碳[9]
- 氰化物[9]
- 乙醇[9]
- 己烷[17]
- 錳乃浦/鋅錳乃浦[5]
- 錳[9][6]
- 汞[9]
- 甲醇[9]
- MPTP[9][18]
- 百草枯[19][5]
- 魚藤酮[19]
- 甲苯[20](吸入濫用)[21]
- 創傷
- 血管的
- Binswanger病(皮質下白質腦病)[9]
- 血管性認知障礙症(多發梗塞性)[9]
- 其他
- 腦幹受損(特別是黑質的多巴胺能核)[22][23]或是基底核(特別是蒼白球)[24]或丘腦的受損[25]
- 甲狀腺機能低下症[9]
- 站立性顫抖症[26]
- 腫瘤伴隨綜合症:因為癌症產生的抗體引發的神經性徵狀[27]
- 快速發作的肌張力障礙性柏金遜症[28]
- 常染色體隱性遺傳性少年柏金遜症[29]
原發性震顫
參考資料
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