嗜铬粒蛋白A
嗜铬细胞瘤
神经内分泌肿瘤
医学
类癌
内分泌系统
甲状腺癌
肺
多发性内分泌肿瘤
类癌
神经母细胞瘤
内科学
病理
内分泌学
甲状腺
生物
免疫组织化学
生物化学
遗传学
激素
基因
细胞培养
作者
Piotr Glinicki,Wojciech Jeske
出处
期刊:Postępy Nauk Medycznych
[Borgis, Ltd.]
日期:2014-11-07
摘要
Summary Chromogranin A (CgA) is a main nonspecific neuroendocrine tumour (NET) marker. Currently few commercial assays are available: RIA, IRMA, ELISA, CLIA, TRACE. There are many factors: in vivo, in vitro and coexisting diseases which can influence the CgA blood concentration. Elevated CgA levels in blood can be usually detected in: gastroenteropancreatic neuroendocrine tumours (GEP-NET), pheochromocytoma, neuroblastoma, MEN syndromes, bronchopulmonary NETs, medullary thyroid carcinoma, small-cell lung carcinoma, and some other very rare NETs. CgA measurement became a routine investigation in the diagnosis of GEP-NET, but is especially helpful in monitoring the effects of their treatment. CgA can be considered as a complementary investigation in the diagnostic procedure of pheochromocytoma. In patients with multiple endocrine neoplasia (MEN) investigation of CgA level may be used in monitoring eventual coexistence or appearance with time of carcinoid, pancreatic neuroendocrine tumour or pheochromocytoma.
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