复发性嗜铬细胞瘤合并胰高血糖素瘤。病例报告。
Recurrent pheochromocytoma associated with glucagonoma. A case report.
作者信息
Yao H, Fukiyama K, Kawano Y, Mizumoto K, Toyoshima S, Omae T
出版信息
Endocrinol Jpn. 1983 Apr;30(2):163-6. doi: 10.1507/endocrj1954.30.163.
PMID:6139277
Abstract
We treated a hypertensive patient with recurrent pheochromocytoma (paraganglioma) associated with glucagonoma. No clinical symptom of glucagonoma was found and it could be detected only by a slight elevation of plasma immunoreactive glucagon (IRG) while the extirpated pancreatic tumor contained much IRG. This case could not be classified as either multiple endocrine neoplasia (MEN) type I or type II.
摘要
我们治疗了一名患有复发性嗜铬细胞瘤（副神经节瘤）并伴有胰高血糖素瘤的高血压患者。未发现胰高血糖素瘤的临床症状，仅通过血浆免疫反应性胰高血糖素（IRG）略有升高才能检测到，而切除的胰腺肿瘤含有大量IRG。该病例不能归类为I型或II型多发性内分泌肿瘤（MEN）。
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