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一名年轻无症状重度高血压患者的副神经节瘤:病例报告及文献综述

Paraganglioma in a young patient with asymptomatic severe hypertension: a case report and review of the literature.

作者信息

Koumaras Ch, Anagnostis P, Tzimou M, Giavanidis I, Gossios Th, Antoniadis A, Athyros V G, Karagiannis A

出版信息

Hippokratia. 2010 Oct;14(4):300-2.

Abstract

We present a case of a 19-year old woman who was admitted to our department with a recently, and incidentally, diagnosed severe hypertension [220/140 mmHg systolic/diastolic blood pressure (BP)]. The patient was asymptomatic. The laboratory investigation demonstrated both elevated plasma norepinephrine (1807 pg/ml, normal range 120-350 pg/ml) and 24h urinary free catecholamines (483 µg/24h, normal range <150 µg/24h), making the diagnosis of a catecholamineproducing tumor highly probable. Although magnetic resonance imaging of the abdomen showed normal adrenal glands, it revealed a mass (4x4 cm) anterior to the inferior vena cava. The diagnosis of paraganglioma was confirmed by the (131)Imeta- iodobenzylguanidine scintigraphy. Preoperatively, α- and β-adrenergic receptor blockers were administered. After successful resection of the tumor, the patient's BP was restored to normal and remained stable during the 3-month follow up. Plasma and 24h urinary catecholamine levels were also normalized. In conclusion, it is important to consider paragangliomas as a possible cause of secondary hypertension and proceed to diagnosis and treatment as described above, since surgical removal of the tumor, especially in sporadic cases, may cure the patient.

摘要

我们报告一例19岁女性患者,她因近期偶然诊断出的重度高血压[收缩压/舒张压220/140 mmHg]入住我科。患者无症状。实验室检查显示血浆去甲肾上腺素升高(1807 pg/ml,正常范围120 - 350 pg/ml)以及24小时尿游离儿茶酚胺升高(483 µg/24小时,正常范围<150 µg/24小时),这使得儿茶酚胺产生肿瘤的诊断极有可能。尽管腹部磁共振成像显示肾上腺正常,但发现下腔静脉前方有一个肿块(4×4 cm)。间碘苄胍闪烁扫描术证实为副神经节瘤。术前给予α和β肾上腺素能受体阻滞剂。成功切除肿瘤后,患者血压恢复正常,在3个月的随访期间保持稳定。血浆和24小时尿儿茶酚胺水平也恢复正常。总之,将副神经节瘤视为继发性高血压的可能病因并按上述方法进行诊断和治疗很重要,因为手术切除肿瘤,尤其是散发性病例,可能治愈患者。

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本文引用的文献

1
Adrenal incidentaloma: a diagnostic challenge.肾上腺偶发瘤:一项诊断挑战。
Hormones (Athens). 2009 Jul-Sep;8(3):163-84. doi: 10.14310/horm.2002.1233.
7
Phaeochromocytoma.嗜铬细胞瘤
Lancet. 2005;366(9486):665-75. doi: 10.1016/S0140-6736(05)67139-5.
9
Current approaches and recommended algorithm for the diagnostic localization of pheochromocytoma.
J Clin Endocrinol Metab. 2004 Feb;89(2):479-91. doi: 10.1210/jc.2003-031091.

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