Marty Cécile, Bennet Antoine, Bayle Paule, Danjoux Marie, Lalande Thibaud, Marguery Marie-Claude, Bazex Jacques
Service de Dermatologie, CHU Purpan, place du Docteur-Baylac, TSA 40031, 31059 Toulouse Cedex 9.
Ann Med Interne (Paris). 2003 Dec;154(8):552-6.
We report a case of glucagonoma syndrome, revealed by a necrolytic migratory erythema that had developed for four Years, associated with anorexia, severe weight loss, anemia, hypoprotidemia, and hypoaminoacidemia. The fasting blood glucose level tended paradoxically to be low (0.6 g/l). Elevated plasma glucagon levels confirmed our diagnosis. The absence of diabetes was explained by an independent insulin secretion derived from this composite pancreatic tumor, authenticated by the histological analysis and the proinsulin level. This level was similar to those typically observed in insulinomas. Six Months after a complete surgical exeresis, symptoms disappeared and biological results returned to normal values.
我们报告一例胰高血糖素瘤综合征病例,患者出现坏死性游走性红斑4年,伴有厌食、严重体重减轻、贫血、低蛋白血症和低氨基酸血症。空腹血糖水平反常地偏低(0.6克/升)。血浆胰高血糖素水平升高证实了我们的诊断。无糖尿病是由该复合性胰腺肿瘤独立分泌胰岛素所致,经组织学分析和胰岛素原水平证实。该水平与胰岛素瘤中通常观察到的水平相似。完整手术切除6个月后,症状消失,生物学检查结果恢复正常。