Normal catecholamine production in a patient with a paroxysmally secreting phaeochromocytoma.

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作者信息

Sinclair D, Shenkin A, Lorimer A R

机构信息

Institute of Biochemistry, Royal Infirmary, Glasgow, UK.

出版信息

Ann Clin Biochem. 1991 Jul;28 ( Pt 4):417-9. doi: 10.1177/000456329102800420.

DOI:10.1177/000456329102800420

PMID:1892355

Abstract

摘要

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引用本文的文献

Current Diagnostic Status of Pheochromocytomaand Future Perspective: A Mini Review.嗜铬细胞瘤的当前诊断现状与未来展望：一篇综述短文

Iran J Pathol. 2017 Summer;12(3):313-322. Epub 2017 Jul 1.

A Rare Case of Adrenal Pheochromocytoma with Unusual Clinical and Biochemical Presentation:  A Case Report and Literature Review.一例肾上腺嗜铬细胞瘤伴不寻常临床和生化表现的罕见病例：病例报告及文献综述

Oman Med J. 2015 Sep;30(5):382-90. doi: 10.5001/omj.2015.76.

Successful pregnancy outcome in a case of pheochromocytoma presenting as severe pre-eclampsia with normal urinary catecholamine level.一例表现为重度子痫前期且尿儿茶酚胺水平正常的嗜铬细胞瘤患者成功妊娠结局。

Indian J Endocrinol Metab. 2013 May;17(3):540-1. doi: 10.4103/2230-8210.111696.

Pheochromocytoma: rediscovery as a catecholamine-metabolizing tumor.嗜铬细胞瘤：作为一种儿茶酚胺代谢肿瘤的重新发现。

Endocr Pathol. 2003 Fall;14(3):193-212. doi: 10.1007/s12022-003-0012-4.

An intra-abdominal tumour.腹腔内肿瘤。

Postgrad Med J. 1997 Jun;73(860):353-5. doi: 10.1136/pgmj.73.860.353.

Biochemical diagnosis of phaeochromocytoma: two instructive case reports.嗜铬细胞瘤的生化诊断：两例指导性病例报告

J Clin Pathol. 1993 Mar;46(3):280-2. doi: 10.1136/jcp.46.3.280.

Lack of uniformity in the clinical approach to the interpretation of urinary catecholamines and their metabolites.在尿儿茶酚胺及其代谢产物解读的临床方法上缺乏一致性。

Ir J Med Sci. 1995 Apr-Jun;164(2):146-50. doi: 10.1007/BF02973283.

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