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一名遗尿男孩在服用丙咪嗪诱发高血压后被诊断为嗜铬细胞瘤。

Pheochromocytoma diagnosed in an enuretic boy after imipramine-induced hypertension.

作者信息

Birkebaek N H, Perrild B D

机构信息

Department of Paediatrics, Herning Hospital, Denmark.

出版信息

Pediatr Hematol Oncol. 1986;3(3):283-5. doi: 10.3109/08880018609031228.

DOI:10.3109/08880018609031228
PMID:3153240
Abstract

A pheochromocytoma was diagnosed in a 14-year-old boy developing hypertension after treatment with imipramine for primary nocturnal enuresis. The mechanism of action is assumed to be an inhibition of the neuronal uptake of catecholamines being released in large quantities from the tumor. The diagnosis of pheochromocytoma should be considered in patients developing hypertension during treatment with cyclic antidepressants.

摘要

一名14岁男孩在用丙咪嗪治疗原发性夜间遗尿症后出现高血压,被诊断为嗜铬细胞瘤。其作用机制被认为是抑制了从肿瘤大量释放的儿茶酚胺的神经元摄取。在用环类抗抑郁药治疗期间出现高血压的患者应考虑嗜铬细胞瘤的诊断。

相似文献

1
Pheochromocytoma diagnosed in an enuretic boy after imipramine-induced hypertension.一名遗尿男孩在服用丙咪嗪诱发高血压后被诊断为嗜铬细胞瘤。
Pediatr Hematol Oncol. 1986;3(3):283-5. doi: 10.3109/08880018609031228.
2
Case records of the Massachusetts General Hospital. Case 16-2005. A nine-year-old girl with headaches and hypertension.马萨诸塞州总医院病例记录。病例16 - 2005。一名患有头痛和高血压的9岁女孩。
N Engl J Med. 2005 May 26;352(21):2223-31. doi: 10.1056/NEJMcpc059011.
3
Pheochromocytoma unmasked by imipramine in an 8-year-old girl.一名8岁女孩因丙咪嗪引发的嗜铬细胞瘤
Pediatr Emerg Care. 2003 Jun;19(3):174-7. doi: 10.1097/01.pec.0000081243.98249.e9.
4
Imipramine-provoked paradoxical pheochromocytoma crisis: a case of cardiogenic shock.丙咪嗪诱发的矛盾性嗜铬细胞瘤危象:一例心源性休克病例
Am J Emerg Med. 1994 Mar;12(2):190-2. doi: 10.1016/0735-6757(94)90245-3.
5
[13-YEAR-OLD GIRL WITH PHEOCHROMOCYTOMA PRESENTING WITH SECONDARY NOCTURNAL ENURESIS].[13岁患嗜铬细胞瘤的女孩出现继发性夜间遗尿症]
Harefuah. 2021 Dec;160(12):818-821.
6
[Pheochromocytoma in children. Two case reports].
Ann Urol (Paris). 2002 Mar;36(2):87-94. doi: 10.1016/s0003-4401(01)00079-1.
7
Clinical imaging rounds: hypertension in a postpartum patient.临床影像病例讨论:产后患者的高血压
N J Med. 1993 Jun;90(6):469-72.
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Hemorrhagic pheochromocytoma presenting as severe hypertension with myocardial infarction.表现为严重高血压并伴有心肌梗死的出血性嗜铬细胞瘤。
Ann Endocrinol (Paris). 2017 Feb;78(1):54-56. doi: 10.1016/j.ando.2016.10.004. Epub 2016 Dec 15.
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[Pheochromocytoma: a hypertensive tumor].
Rev Infirm. 2003 Dec(96):29.
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[Diagnosis and therapy of hypertension due to pheochromocytoma].[嗜铬细胞瘤所致高血压的诊断与治疗]
Zentralbl Chir. 1969 Feb 8;94(6):177-87.

引用本文的文献

1
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.
2
Understanding catecholamine metabolism as a guide to the biochemical diagnosis of pheochromocytoma.将儿茶酚胺代谢作为嗜铬细胞瘤生化诊断的指导依据。
Rev Endocr Metab Disord. 2001 Aug;2(3):297-311. doi: 10.1023/a:1011572617314.