Moattari A R, Cho K, Vinik A I
Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor.
Surgery. 1990 Sep;108(3):581-7.
After an acute episode of pancreatitis, a 63-year-old man was found to have a pancreatic glucagonoma. The tumor was resected without evidence of metastases. Three years later he had symptoms of uncontrolled diabetes, no skin lesions, and diarrhea and was found to have a pancreatic pseudocyst and multiple hepatic metastases. Glucagon concentrations were raised but were suppressible by glucose and somatostatin and responded to arginine stimulation. He was treated for 6 months with octreotide (Sandostatin), which reduced his symptoms; the pseudocyst resolved, but liver metastases continued to grow. Although spontaneous resolution of the pseudocyst is possible, this case appears to illustrate differences in sensitivity of endocrine and exocrine tissues to suppression by Sandostatin.
在一次急性胰腺炎发作后,一名63岁男性被发现患有胰腺高血糖素瘤。肿瘤被切除,未发现转移迹象。三年后,他出现了糖尿病控制不佳的症状,无皮肤病变,伴有腹泻,并且发现有胰腺假性囊肿和多处肝转移。高血糖素浓度升高,但可被葡萄糖和生长抑素抑制,并对精氨酸刺激有反应。他接受了6个月的奥曲肽(善宁)治疗,症状有所减轻;假性囊肿消退,但肝转移继续发展。虽然假性囊肿有可能自行消退,但该病例似乎说明了内分泌和外分泌组织对善宁抑制的敏感性差异。