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GLUCAGONOMA SYNDROME WITH INCREASED LACTATE DEHYDROGENASE ISOENZYMES: OCTREOTIDE TREATMENT

 

作者: Gregory M. Siller,   Geoffrey M. Strutton,   Geoffrey A. Moore,   David M. Kanowski And,   Judith A. Nedwich,  

 

期刊: Australasian Journal of Dermatology  （WILEY Available online 1994）
卷期: Volume 35, issue 1  

页码: 11-14

 

ISSN:0004-8380

 

年代: 1994

 

DOI:10.1111/j.1440-0960.1994.tb01792.x

 

出版商: Blackwell Publishing Ltd

 

关键词: Glucagonoma Syndrome;Octreotide;Lactate dehydrogenase;Multiple Endocrine Neoplasia

 

数据来源: WILEY

 

摘要:

SUMMARYGlucagonoma Syndrome is a rare syndrome comprising hyperglucagonemia, diabetes mellitus, necrolytic migratory erythema and hypoaminoacidemia in the setting of a glucagon producing, alpha cell tumour of the pancreas. We report a case of Glucagonoma Syndrome palliatively treated successfully with octreotide. In addition to classical clinical and biochemical findings, this patient also had a Glomus Jugulars tumour, and Empty Sella Syndrome and demonstrated an unusual pattern of plasma lactate dehydrogenase isoenzymes, features not previously reported in this syndrome.

 

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