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继发于压迫性颅咽管瘤的左旋多巴反应性帕金森综合征:一例报告

Levodopa-Responsive Parkinsonian Syndrome Secondary to a Compressive Craniopharyngioma: A Case Report.

作者信息

Rodriguez Wilson, Fedorova Margarita, Chand Pratap

机构信息

Neurology, Saint Louis University School of Medicine, Saint Louis, USA.

出版信息

Cureus. 2023 Feb 28;15(2):e35621. doi: 10.7759/cureus.35621. eCollection 2023 Feb.

DOI:10.7759/cureus.35621
PMID:37007394
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10065367/
Abstract

Parkinsonism is a rare manifestation of brain tumors that has most commonly been reported in association with gliomas and meningiomas. In this paper, we describe a unique case of secondary Parkinsonism that was precipitated by a craniopharyngioma. A 42-year-old female presented with resting tremors, rigidity, and bradykinesia. Her past medical history was significant for a craniopharyngioma resection four months prior. The postoperative course was complicated by severe delirium, panhypopituitarism, and diabetes insipidus. Notably, she was taking haloperidol and aripiprazole daily for four months to manage her delirium and psychotic episodes. Her preoperative brain MRI showed a compressive effect of the craniopharyngioma on the midbrain and nigrostriatum. Drug-induced Parkinsonism was initially suspected given extended treatment with antipsychotics. Haloperidol and aripiprazole were stopped, and benztropine was started with no improvement. Consequently, the patient was treated with carbidopa/levodopa with symptomatic improvement. A dopamine transporter (DaT) scan was done after starting carbidopa/levodopa and showed asymmetric decreased uptake in dopamine transporter in the striatum. Only one other case of Parkinsonism following craniopharyngioma resection was found in the literature review. Unlike our example, the symptoms resolved following surgical intervention and did not require a long-term treatment with carbidopa/levodopa. The purpose of our case report is to highlight brain tumors as a potential cause of secondary Parkinsonism in younger patients for an early surgical intervention can be curative.

摘要

帕金森综合征是脑肿瘤的一种罕见表现,最常见于与胶质瘤和脑膜瘤相关的报道中。在本文中,我们描述了一例由颅咽管瘤引发的继发性帕金森综合征的独特病例。一名42岁女性出现静止性震颤、僵硬和运动迟缓。她的既往病史中,四个月前有过颅咽管瘤切除术,术后过程并发严重谵妄、全垂体功能减退和尿崩症。值得注意的是,她连续四个月每天服用氟哌啶醇和阿立哌唑来控制谵妄和精神症状。她术前的脑部MRI显示颅咽管瘤对中脑和黑质纹状体有压迫作用。鉴于使用抗精神病药物进行了长期治疗,最初怀疑是药物性帕金森综合征。停用了氟哌啶醇和阿立哌唑,并开始使用苯海索,但没有改善。因此,患者接受了卡比多巴/左旋多巴治疗,症状有所改善。开始使用卡比多巴/左旋多巴后进行了多巴胺转运体(DaT)扫描,结果显示纹状体中多巴胺转运体摄取不对称减少。在文献综述中仅发现另一例颅咽管瘤切除术后发生帕金森综合征的病例。与我们的病例不同,该病例的症状在手术干预后得到缓解,不需要长期使用卡比多巴/左旋多巴治疗。我们病例报告的目的是强调脑肿瘤是年轻患者继发性帕金森综合征的潜在原因,因为早期手术干预可能治愈。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4def/10065367/8afbe1663082/cureus-0015-00000035621-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4def/10065367/7f2c3b623fb7/cureus-0015-00000035621-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4def/10065367/8afbe1663082/cureus-0015-00000035621-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4def/10065367/7f2c3b623fb7/cureus-0015-00000035621-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4def/10065367/8afbe1663082/cureus-0015-00000035621-i02.jpg

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本文引用的文献

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Brain Tumor Presenting with Parkinsonism.以帕金森综合征为表现的脑肿瘤
Case Rep Neurol. 2021 Sep 13;13(3):595-597. doi: 10.1159/000518198. eCollection 2021 Sep-Dec.
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Craniopharyngioma.颅咽管瘤。
Nat Rev Dis Primers. 2019 Nov 7;5(1):75. doi: 10.1038/s41572-019-0125-9.
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Molecular Imaging of the Dopamine Transporter.多巴胺转运体的分子影像学研究
Cells. 2019 Aug 10;8(8):872. doi: 10.3390/cells8080872.
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Parkinsonism: a rare manifestation of craniopharyngioma.帕金森症:颅咽管瘤的一种罕见表现。
Electron Physician. 2015 Jun 5;7(2):1027-31. doi: 10.14661/2015.1027-1031. eCollection 2015 Apr-Jun.
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Pathophysiology of parkinsonism.帕金森病的病理生理学
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The descriptive epidemiology of craniopharyngioma.颅咽管瘤的描述性流行病学。
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