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嗜铬细胞瘤的诊断与定位

Diagnosis and localization of pheochromocytoma.

作者信息

Goldstein David S, Eisenhofer Graeme, Flynn John A, Wand Gary, Pacak Karel

机构信息

Clinical Neurocardiology Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Md 20892-1620, USA.

出版信息

Hypertension. 2004 May;43(5):907-10. doi: 10.1161/01.HYP.0000125014.56023.b8. Epub 2004 Mar 15.

DOI:10.1161/01.HYP.0000125014.56023.b8
PMID:15023935
Abstract

This Hypertension Grand Rounds shows how applying new clinical laboratory techniques helped to diagnose pheochromocytoma in a difficult case. In the setting of long-standing, sustained hypertension, the patient had a hypertensive paroxysm during anesthesia induction for surgery, leading to suspicion of a pheochromocytoma. Conventional testing, including CT scanning and fractionated urinary metanephrine test, was not diagnostic. The patient had another hypertensive paroxysm during subsequent anesthesia induction, requiring intensive care. Consistently elevated plasma levels of free normetanephrine provided the first and only biochemical evidence for a pheochromocytoma in this case. 6-[18F]Fluorodopamine positron emission tomography and 123I-metaiodobenzylguanidine scintigraphy subsequently agreed on the existence of a small left adrenal mass, which when removed surgically proved to be a pheochromocytoma. Postoperatively, plasma levels of normetanephrine normalized, and there were no further hypertensive paroxysms, although the patient remained hypertensive. This case illustrates the superiority of plasma levels of free (unconjugated) metanephrines, compared with other biochemical tests, to detect pheochromocytoma. It also confirms that functional imaging by 6-[18F]fluorodopamine or 123I-metaiodobenzylguanidine scanning can localize pheochromocytoma in difficult cases in which other imaging tests are not diagnostic.

摘要

本次高血压病例讨论会展示了如何运用新的临床实验室技术,在一例疑难病例中协助诊断嗜铬细胞瘤。在长期持续性高血压的背景下,该患者在手术麻醉诱导期间出现高血压发作,从而引发了对嗜铬细胞瘤的怀疑。包括CT扫描和尿分馏甲氧基肾上腺素检测在内的传统检查均未得出诊断结果。患者在随后的麻醉诱导过程中再次出现高血压发作,需要重症监护。游离去甲肾上腺素血浆水平持续升高,为该病例中的嗜铬细胞瘤提供了首个也是唯一的生化证据。随后,6-[18F]氟多巴胺正电子发射断层扫描和123I-间碘苄胍闪烁扫描均证实左肾上腺存在一个小肿块,手术切除后证实为嗜铬细胞瘤。术后,去甲肾上腺素血浆水平恢复正常,尽管患者仍有高血压,但未再出现高血压发作。该病例说明了游离(未结合)甲氧基肾上腺素血浆水平在检测嗜铬细胞瘤方面优于其他生化检测。它还证实,在其他影像学检查无法诊断的疑难病例中,通过6-[18F]氟多巴胺或123I-间碘苄胍扫描进行功能成像能够定位嗜铬细胞瘤。

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