Nakajima Rikako, Sato Daisuke, Togashi Ichirota, Idesawa Hiroto, Ito Jun, Ito Kei, Fujii Masanao, Yagyu Hiroaki
Department of Endocrinology and Metabolism, Tsukuba University Hospital Mito Clinical Education and Training Center, Mito Kyodo General Hospital, Mito, Ibaraki, Japan.
Endocrinol Diabetes Metab Case Rep. 2024 Aug 12;2024(3). doi: 10.1530/EDM-24-0062. Print 2024 Jul 1.
An 89-year-old woman presented with a 6-year history of occasional episodes of impaired consciousness that were relieved by ingestion of a snack. Three months before presenting to our hospital, she had been hospitalized in a local hospital with subdural hematoma caused by a head contusion, where previously unrecognized hypoglycemia was discovered. Fasting plasma glucose concentration was 37 mg/dL, with a relatively high serum level of insulin (34.9 µU/mL). Computed tomography showed a 14 mm hyperenhancing tumor in the tail of the pancreas and she was referred to our hospital for further investigation. A prolonged fasting test revealed the plasma glucose concentration reduced to 43 mg/dL (2.4 mmol/L) at 8 h after the last meal. Serum insulin, proinsulin, and C-peptide concentrations were 21.1 µU/mL, 16.9 pmol/L, and 2.72 ng/mL, respectively. Subsequent intravenous administration of 1 mg of glucagon increased the plasma glucose concentration to 76 mg/dL (4.2 mmol/L). Moreover, the insulin-to-C-peptide molar ratio was 0.14. These data indicated the presence of insulinoma. Interestingly, serum anti-insulin antibodies were elevated (21.1 U/mL), although she had no history of taking exogenous insulin injection, alpha lipoic acid, or sulfhydryl group-containing agents. Human leukocyte antigen (HLA) typing revealed HLA-DRB10407 and HLA-DRB11405 alleles. Treatment with diazoxide prevented hypoglycemia, but was discontinued due to weight gain and leg edema. Elevated serum anti-insulin antibodies persisted almost 1 year after the diagnosis of insulinoma. We present a rare case of insulinoma concomitant with serum anti-insulin antibodies.
Insulinoma presenting with concomitant anti-insulin antibodies appears rare. Insulin/C-peptide molar ratio and serum insulin concentration are useful for differentiating insulinoma and autoimmune syndrome. Flash glucose monitoring systems appear suitable for evaluating treatment outcomes.
一名89岁女性有6年偶尔意识障碍发作史,进食零食后可缓解。在我院就诊前3个月,她因头部挫伤导致硬膜下血肿入住当地医院,在那里发现了此前未被识别的低血糖。空腹血糖浓度为37mg/dL,胰岛素血清水平相对较高(34.9µU/mL)。计算机断层扫描显示胰腺尾部有一个14mm的强化肿瘤,她被转诊至我院进一步检查。延长禁食试验显示,最后一餐8小时后血浆葡萄糖浓度降至43mg/dL(2.4mmol/L)。血清胰岛素、胰岛素原和C肽浓度分别为21.1µU/mL、16.9pmol/L和2.72ng/mL。随后静脉注射1mg胰高血糖素使血浆葡萄糖浓度升至76mg/dL(4.2mmol/L)。此外,胰岛素与C肽的摩尔比为0.14。这些数据表明存在胰岛素瘤。有趣的是,尽管她没有注射外源性胰岛素、α硫辛酸或含巯基药物的病史,但血清抗胰岛素抗体升高(21.1U/mL)。人类白细胞抗原(HLA)分型显示HLA-DRB10407和HLA-DRB11405等位基因。用二氮嗪治疗可预防低血糖,但因体重增加和腿部水肿而停药。胰岛素瘤诊断后,血清抗胰岛素抗体升高持续了近1年。我们报告了一例罕见的伴有血清抗胰岛素抗体的胰岛素瘤病例。
伴有抗胰岛素抗体的胰岛素瘤似乎很罕见。胰岛素/C肽摩尔比和血清胰岛素浓度有助于区分胰岛素瘤和自身免疫综合征。动态血糖监测系统似乎适合评估治疗效果。