Lefebvre J, Lelièvre G, Dalle-Furnari M A, Proye C, Mazzuca M, Garraud J C, Luyckx A, Linquette M
Diabete Metab. 1982 Sep;8(3):191-5.
Diabetic ketoacidosis is an extremely rare manifestation of glucagonoma. We report such a case in a 72-year-old woman known to be diabetic for seven years. The patient was admitted with diabetic ketoacidosis and associated necrolytic migratory erythrema which suggested the diagnosis of glucagonoma. Plasma glucagon levels were increased (569 to 2298 pg/ml). A vascular tumor of the head of the pancreas without obvious hepatic metastases was visualised by angiography. Duodeno-pancreatectomy including the head of the pancreas led to complete recovery of the mucocutaneous lesions and the plasma glucagon level fell (229 pg/ml). The tumor had several histological characteristics suggesting malignancy and a high glucagon content on extraction. Electron microscopy showed multiple A cells and a few isolated B cells. Most of the cells showed immunoreactivity with anti-glucagon and anti-glicentine antibodies. Three months after surgery, the diabetes was again required treatment with insulin. Plasma glucagon level was again increased and chemotherapy with dimethyltriazenimidazolecarboxamide was undertaken.
糖尿病酮症酸中毒是胰高血糖素瘤极为罕见的一种表现形式。我们报告了一例72岁女性患者,该患者已知患有糖尿病七年。患者因糖尿病酮症酸中毒及相关的坏死松解性游走性红斑入院,这提示了胰高血糖素瘤的诊断。血浆胰高血糖素水平升高(569至2298皮克/毫升)。血管造影显示胰腺头部有一个无明显肝转移的血管性肿瘤。包括胰腺头部的十二指肠-胰腺切除术使皮肤黏膜病变完全恢复,血浆胰高血糖素水平下降(229皮克/毫升)。该肿瘤具有若干提示恶性的组织学特征,提取时胰高血糖素含量较高。电子显微镜检查显示有多个A细胞和一些孤立的B细胞。大多数细胞与抗胰高血糖素和抗甘丙肽抗体呈免疫反应。术后三个月,糖尿病再次需要胰岛素治疗。血浆胰高血糖素水平再次升高,遂进行了二甲基三氮烯咪唑甲酰胺化疗。