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嗜铬细胞瘤的模拟——孟乔森综合征。

Simulation of a pheochromocytoma--Munchausen syndrome.

作者信息

Spitzer D, Bongartz D, Ittel T H, Sieberth H G

机构信息

Medizinische Klinik II, Universitätsklinikum der RWTH Aachen, Pauwelsstrasse 30, D-52074 Aachen, Germany.

出版信息

Eur J Med Res. 1998 Dec 16;3(12):549-53.

PMID:9889174
Abstract

A 46-year old female nursing sister was admitted to three different hospitals because of blood pressure crises of 300/150 mmHg which occurred up to six times a day. The rises in blood pressure were accompanied by headache, tachycardia and outbreaks of sweating. Raised catecholamine concentrations were repeatedly measured in the 24-hour urine and in the blood. The diagnosis of pheochromocytoma could therefore be regarded as confirmed. The investigations to establish the localization (including MIBG scintigrams carried out several times) showed negative results. Octreotide scintigraphy finally revealed a raised concentration of nuclides in the right adrenals. Selective venous blood samples showed markedly raised concentrations of adrenaline and noradrenaline in all regions investigated. After removing the right adrenal, which was of normal histological appearance, there was an improvement for six months. Afterwards, up to six blood pressure crises per day were observed once more. Fresh determination of catecholamines at various levels demonstrated the highest concentrations in the left iliac vein. It was then shown that the patient injected catecholamines intravaginally even during the angiographic investigation. A search of the patient s room revealed several ampoules containing noradrenaline and adrenaline as well as syringes and needles. - This case shows that in clinical pictures with typical clinical symptoms and negative results of repeated investigations a factitious disorder must be considered in terms of differential diagnosis especially when female patients with medical knowledge who have ready access to drugs are involved with a history comprising several stays in hospital which have not produced any clarification of their condition.

摘要

一名46岁的女性护士因每天出现多达6次的300/150 mmHg血压危机而被送往三家不同的医院。血压升高伴有头痛、心动过速和出汗发作。24小时尿液和血液中多次检测到儿茶酚胺浓度升高。因此,嗜铬细胞瘤的诊断可被视为得到证实。确定肿瘤位置的检查(包括多次进行的间碘苄胍闪烁扫描)结果均为阴性。奥曲肽闪烁扫描最终显示右肾上腺核素浓度升高。选择性静脉血样显示,在所有检测区域,肾上腺素和去甲肾上腺素的浓度均显著升高。切除组织学外观正常的右肾上腺后,病情有六个月的改善。之后,再次观察到每天出现多达6次的血压危机。对不同水平的儿茶酚胺进行重新检测发现,左髂静脉中的浓度最高。随后发现,即使在血管造影检查期间,该患者仍通过阴道内注射儿茶酚胺。搜查患者病房时发现了几个装有去甲肾上腺素和肾上腺素的安瓿以及注射器和针头。——该病例表明,对于具有典型临床症状且多次检查结果为阴性的临床情况,在鉴别诊断时必须考虑人为障碍,尤其是当涉及有医学知识且能轻易获取药物的女性患者,且其病史包括多次住院但病情仍未明确时。

相似文献

1
Simulation of a pheochromocytoma--Munchausen syndrome.嗜铬细胞瘤的模拟——孟乔森综合征。
Eur J Med Res. 1998 Dec 16;3(12):549-53.
2
The catecholamine concentration in central veins of hypertensive patients--an aid not without problems in locating phaeochromocytoma.高血压患者中心静脉中儿茶酚胺的浓度——这在定位嗜铬细胞瘤时并非没有问题的一种辅助手段。
Acta Chir Scand Suppl. 1986;530:67-71.
3
[Personal experience in diagnosis and localization of pheochromocytoma].[嗜铬细胞瘤诊断与定位的个人经验]
Srp Arh Celok Lek. 2002 Jul;130 Suppl 2:14-9.
4
[Test with clonidine for diagnosing pheochromocytoma].
Pol Tyg Lek. 1991;46(35-36):641-5.
5
[Rare cases of pheochromocytoma. A report of two cases].
Hinyokika Kiyo. 1985 Aug;31(8):1427-32.
6
[Usefulness of determining conjugated amine catecholamines in blood platelets for diagnosis of pheochromocytoma].
Pol Tyg Lek. 1991;46(35-36):646-8.
7
Plasma neuropeptide Y immunoreactivity influences left ventricular mass in pheochromocytoma.血浆神经肽Y免疫反应性影响嗜铬细胞瘤患者的左心室质量。
Clin Chim Acta. 2004 Jul;345(1-2):43-7. doi: 10.1016/j.cccn.2004.01.027.
8
Localization of pheochromocytoma by selective venous catheterization and assay of plasma catecholamines.通过选择性静脉插管和血浆儿茶酚胺测定对嗜铬细胞瘤进行定位。
Can Med Assoc J. 1979 Mar 3;120(5):539-42.
9
Catecholamine release after physical exercise. A new provocative test for early diagnosis of pheochromocytoma in multiple endocrine neoplasia type 2.
Acta Med Scand. 1987;222(4):351-9.
10
[Evaluation of the usefulness for measuring catecholamines and their principle metabolites in the diagnosis of pheochromocytoma].[评估儿茶酚胺及其主要代谢产物测定在嗜铬细胞瘤诊断中的应用价值]
Przegl Lek. 1997;54(11):793-8.

引用本文的文献

1
Münchausen Syndrome as an Unusual Cause of Pseudo-resistant Hypertension: A Case Report.孟乔森综合征作为假性难治性高血压的罕见病因:一例报告
Open Med (Wars). 2019 Nov 7;14:792-796. doi: 10.1515/med-2019-0094. eCollection 2019.
2
Factitious Cushing's Syndrome: A Diagnosis to Consider When Evaluating Hypercortisolism.假性库欣综合征:评估皮质醇增多症时需考虑的一种诊断。
Front Endocrinol (Lausanne). 2019 Mar 4;10:129. doi: 10.3389/fendo.2019.00129. eCollection 2019.
3
Severe and refractory hypertension in a young woman.一名年轻女性的重度难治性高血压
J Am Soc Hypertens. 2016 Jun;10(6):506-9. doi: 10.1016/j.jash.2016.03.193. Epub 2016 Apr 4.
4
Tachyarrythmias with elevated cardiac enzymes in Münchausen syndrome.心脏酶升高的人为性心动过速综合征。
Clin Auton Res. 2010 Aug;20(4):259-61. doi: 10.1007/s10286-010-0066-6. Epub 2010 Apr 28.
5
Pheochromocytoma or Münchausen syndrome: the masquerade is up.嗜铬细胞瘤还是孟乔森综合征:伪装已被识破。
Clin Auton Res. 2010 Aug;20(4):211-2. doi: 10.1007/s10286-010-0067-5. Epub 2010 Apr 27.
6
Adverse drug reactions in patients with phaeochromocytoma: incidence, prevention and management.嗜铬细胞瘤患者的药物不良反应:发生率、预防及管理
Drug Saf. 2007;30(11):1031-62. doi: 10.2165/00002018-200730110-00004.