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本文引用的文献

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Neuroleptic malignant syndrome versus serotonin syndrome: the search for a diagnostic tool.神经阻滞剂恶性综合征与血清素综合征:寻找诊断工具。
Ann Pharmacother. 2011 Sep;45(9):e50. doi: 10.1345/aph.1P787. Epub 2011 Aug 30.
2
Phaeochromocytoma: diagnostic challenges for biochemical screening and diagnosis.嗜铬细胞瘤:生化筛查和诊断的挑战。
J Clin Pathol. 2010 Aug;63(8):669-74. doi: 10.1136/jcp.2009.071647. Epub 2010 Jun 14.
3
Radiation dose associated with common computed tomography examinations and the associated lifetime attributable risk of cancer.与常见计算机断层扫描检查相关的辐射剂量及相关的终生可归因癌症风险。
Arch Intern Med. 2009 Dec 14;169(22):2078-86. doi: 10.1001/archinternmed.2009.427.
4
False positive test results for pheochromocytoma from 2000 to 2008.2000年至2008年嗜铬细胞瘤的假阳性检测结果。
Exp Clin Endocrinol Diabetes. 2010 Oct;118(9):577-85. doi: 10.1055/s-0029-1237699. Epub 2009 Dec 8.
5
The catatonia syndrome: forgotten but not gone.紧张症综合征:被遗忘却未消逝。
Arch Gen Psychiatry. 2009 Nov;66(11):1173-7. doi: 10.1001/archgenpsychiatry.2009.141.
6
Catatonia: a syndrome appears, disappears, and is rediscovered.紧张症:一种综合征反复出现、消失又被重新发现。
Can J Psychiatry. 2009 Jul;54(7):437-45. doi: 10.1177/070674370905400704.
7
Malignant catatonia accompanied by high urinary catecholamine levels mimicking the presentation of pheochromocytoma.恶性紧张症伴高尿儿茶酚胺水平,酷似嗜铬细胞瘤的表现。
Psychiatry Clin Neurosci. 2009 Jun;63(3):428-9. doi: 10.1111/j.1440-1819.2009.01962.x.
8
The protean manifestations of pheochromocytoma.嗜铬细胞瘤的多种表现。
Horm Metab Res. 2009 Sep;41(9):658-63. doi: 10.1055/s-0028-1128139. Epub 2009 Feb 25.
9
Advances in biochemical screening for phaeochromocytoma using biogenic amines.利用生物胺进行嗜铬细胞瘤生化筛查的进展
Clin Biochem Rev. 2009 Feb;30(1):3-17.
10
Delirious mania and malignant catatonia: a report of 3 cases and review.谵妄性躁狂与恶性紧张症:3例报告及文献复习
Psychiatr Q. 2009 Mar;80(1):23-40. doi: 10.1007/s11126-009-9091-9. Epub 2009 Feb 6.

模仿嗜铬细胞瘤的恶性紧张症。

Malignant catatonia mimicking pheochromocytoma.

作者信息

Wong Sophia, Hughes Barbara, Pudek Morris, Li Dailin

机构信息

Department of Pathology and Laboratory Medicine, University of British Columbia, 855 West 12th Avenue, Vancouver, BC, Canada V5Z 1M9.

出版信息

Case Rep Endocrinol. 2013;2013:815821. doi: 10.1155/2013/815821. Epub 2013 Oct 22.

DOI:10.1155/2013/815821
PMID:24251048
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3819819/
Abstract

Malignant catatonia is an unusual and highly fatal neuropsychiatric condition which can present with clinical and biochemical manifestations similar to those of pheochromocytoma. Differentiating between the two diseases is essential as management options greatly diverge. We describe a case of malignant catatonia in a 20-year-old male who presented with concurrent psychotic symptoms and autonomic instability, with markedly increased 24-hour urinary levels of norepinephrine at 1752 nmol/day (normal, 89-470 nmol/day), epinephrine at 1045 nmol/day (normal, <160 nmol/day), and dopamine at 7.9  μ mol/day (normal, 0.4-3.3  μ mol/day). The patient was treated with multiple sessions of electroconvulsive therapy, which led to complete clinical resolution. Repeat urine collections within weeks of this presenting event revealed normalization or near normalization of his catecholamine and metanephrine levels. Malignant catatonia should be considered in the differential diagnosis of the hypercatecholamine state, particularly in a patient who also exhibits concurrent catatonic features.

摘要

恶性紧张症是一种罕见且致死率很高的神经精神疾病,其临床和生化表现可能与嗜铬细胞瘤相似。由于两种疾病的治疗方法差异很大,因此进行鉴别诊断至关重要。我们报告一例20岁男性恶性紧张症患者,该患者同时出现精神病性症状和自主神经功能不稳定,24小时尿去甲肾上腺素水平显著升高,达1752 nmol/天(正常范围89 - 470 nmol/天),肾上腺素水平为1045 nmol/天(正常范围<160 nmol/天),多巴胺水平为7.9 μmol/天(正常范围0.4 - 3.3 μmol/天)。该患者接受了多次电休克治疗,临床症状完全缓解。在此次发病数周内再次收集尿液显示,其儿茶酚胺和甲氧基肾上腺素水平恢复正常或接近正常。在鉴别诊断高儿茶酚胺状态时,应考虑恶性紧张症,尤其是在同时伴有紧张症特征的患者中。