Holstein Andreas, Morgenstern Thomas, Dienst Henry, Hiller Wolfgang
Department of Gastroenterology, Lippe-Detmold Hospital.
Department of Surgery, Lippe-Detmold Hospital, Detmold, Germany.
J Obstet Gynaecol Res. 2015 Nov;41(11):1848-50. doi: 10.1111/jog.12785. Epub 2015 Sep 24.
Post-partum hypoglycemia in non-diabetic women is a rare condition. We report the exceptional case of a 38-year-old obese woman who experienced recurrent neuroglycopenia 3 weeks after delivery. Corresponding to severe hypoglycemia with blood glucose levels of <30 mg/dL, there was no suppression of insulin or C-peptide. Through endoscopic ultrasound we detected a hypoechoic lesion of 8 × 9 mm localized in the head of the pancreas. Thus, the diagnosis of insulinoma was most probable. Complete surgical enucleation of the insulinoma resulted in immediate and permanent resolution of hypoglycemia. The postoperative course was complicated by recurrent episodes of pancreatitis requiring endoscopic ultrasound-guided punctures of pseudocysts and temporary stenting of the pancreatic duct. In conclusion, insulinoma is a very rare, nonetheless important, differential diagnosis of post-partum hypoglycemia.
非糖尿病女性产后低血糖是一种罕见病症。我们报告了一例特殊病例,一名38岁肥胖女性在分娩后3周出现反复性神经低血糖症。对应严重低血糖,血糖水平<30mg/dL,胰岛素或C肽未被抑制。通过内镜超声,我们在胰头检测到一个8×9mm的低回声病变。因此,最有可能的诊断是胰岛素瘤。胰岛素瘤完整手术摘除导致低血糖立即且永久缓解。术后病程因胰腺炎反复发作而复杂化,需要内镜超声引导下穿刺假性囊肿并临时置入胰管支架。总之,胰岛素瘤是产后低血糖一种非常罕见但很重要的鉴别诊断。