Sunder Ashok, Saha Sudip, Satyanarayan Bhagyalakshmi, Kumar Manish, Sarkar Nilanjan
Department of General Medicine, Tata Main Hospital, Tata Steel, Jamshedpur, Jharkhand, India.
J Family Med Prim Care. 2022 Sep;11(9):5696-5699. doi: 10.4103/jfmpc.jfmpc_333_22. Epub 2022 Oct 14.
Insulinoma is a rare pancreatic neuroendocrine tumour (PNET) with an incidence rate of 4 per million population, and the most common cause of hypoglycaemia due to endogenous hyperinsulinism. We present the story of a 61-year-old male, who was extensively evaluated at many hospitals for his symptoms of giddiness, uneasiness and recurrent black outs for the last 3 months, his symptoms disappearing with a carbohydrate rich meal or sweets. Random sugar and fasting sugar values noted were low, with elevated insulin and C-peptide levels. Diagnosis of insulinoma was confirmed by a DOTA PET scan involving the tail of the pancreas and then surgically removed. Early detection is crucial for early surgery to allay symptoms. We describe our diagnostic and treatment plan with reference to previously published reports.
胰岛素瘤是一种罕见的胰腺神经内分泌肿瘤(PNET),发病率为百万分之四,是内源性高胰岛素血症导致低血糖的最常见原因。我们讲述一位61岁男性的病例,在过去3个月里,他因头晕、不适和反复晕厥症状在多家医院接受了全面检查,食用富含碳水化合物的食物或糖果后症状消失。随机血糖和空腹血糖值较低,胰岛素和C肽水平升高。通过涉及胰尾的DOTA PET扫描确诊为胰岛素瘤,随后进行了手术切除。早期发现对于早期手术缓解症状至关重要。我们参考先前发表的报告描述了我们的诊断和治疗方案。