Lenka Nosakova, Peter Banovcin, Martin Duricek, Peter Uhrik, Janka Bozikova, Michal Demeter, Rudol Hyrdel
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引用次数: 0
Abstract
Introduction: Insulinomas are rare neuroendocrine tumors of pancreas. Clinical manifestations include various symptoms of hypoglycemia, which is the result of insulin overproduction. Symptoms of hypoglycemia are heterogenous what most probably contributes to diagnostic delay. In this study we retrospectively evaluated clinical features of hypoglycemia. We discovered that a substantial number of patients suffered from hypoglycemia unawareness.
Materials and methods: We performed retrospective analysis of prospectively collected patients with histologically confirmed insulinoma. We evaluated clinical features and signs of hypoglycemia and the duration of symptoms and performed thorough review of the patients' files in order to identify whether patients had been falsely diagnosed previously. Each patient underwent 72 hour fasting test during which levels of immunoreactive insulin (IRI), C-peptide and nadir blood glucose level were obtained. Based on the clinical findings and results of 72 hour fasting test we identified a subgroup of patients with hypoglycemia unawareness. These had an episode of clinically silent hypoglycemia. We compared IRI and C-peptide levels obtained at the time of the fasting test termination in the unawareness group and the group without hypoglycemia unawareness.
Results: Twenty two patients with insulinoma that had been hospitalized in our tertiary center were included in the analysis. Mean age was 51±16.7 years. The most common symptom reported by 63.6% of patients was fatigue, followed by increased appetite with consequent weight gain and the loss of consciousness, both reported by 40.9% of patients. Based on the review of clinical features and the results of the fasting test we identified a group of patients with hypoglycemia unawareness. We labeled the patient accordingly in case of the loss of consciousness in personal history as well as asymptomatic hypoglycemia or severe neuroglycopenic symptoms during the fasting test without any accompanying or preceding clinical signs. There were 7 patients with hypoglycemia unawareness in our cohort (31.8%). Patients with this phenomenon had significantly lower levels of both IRI (2.35±1.25 vs. 5.88±3.92ng/ml, p=0.01) and C-peptide (9.14±7.36 vs. 50±42.8 µU/ml, p=0.01) than the rest of the patients. Nadir blood glucose level during the fasting test showed no significant difference (9.4±8.2 vs. 12.2±8.2 months, p=0.28) in the unawareness group and the rest of the patients, respectively.
Conclusion: We described the phenomenon of unawareness to hypoglycemia in the patients with insulinoma. This has not been recognized in insulinoma patients yet since available evidence mostly relates to type I diabetic patients. It might lead to higher morbidity and diagnostic delay. Further studies with prospective evaluation should be performed to further confirm relatively high prevalence in patients with insulinoma.
导言胰岛素瘤是一种罕见的胰腺神经内分泌肿瘤。临床表现包括各种低血糖症状,这是胰岛素分泌过多的结果。低血糖的症状多种多样,这很可能是导致诊断延误的原因。在这项研究中,我们对低血糖的临床特征进行了回顾性评估。我们发现,相当多的患者对低血糖症一无所知:我们对前瞻性收集的经组织学证实的胰岛素瘤患者进行了回顾性分析。我们评估了低血糖的临床特征和体征以及症状持续时间,并对患者档案进行了全面审查,以确定患者之前是否曾被误诊。每位患者都接受了 72 小时的空腹测试,在测试过程中获得了免疫反应性胰岛素(IRI)、C 肽和最低血糖水平。根据临床发现和 72 小时空腹测试结果,我们确定了一个低血糖无意识患者亚群。这些患者曾发生过临床上无症状的低血糖。我们比较了无低血糖意识组和无低血糖意识组在空腹测试终止时获得的 IRI 和 C 肽水平:分析对象包括在本三级医疗中心住院治疗的 22 名胰岛素瘤患者。平均年龄为 51±16.7 岁。63.6%的患者报告的最常见症状是疲劳,其次是食欲增加导致体重增加和意识丧失,这两种症状均有40.9%的患者报告。根据临床特征和空腹测试结果,我们确定了一组低血糖无意识症患者。如果患者在个人病史中出现意识丧失、无症状性低血糖或在空腹测试中出现严重的神经性低血糖症状,但没有任何伴随或先兆临床症状,我们就会给患者贴上相应的标签。我们的队列中有 7 名低血糖无意识患者(31.8%)。与其他患者相比,有这种现象的患者的 IRI(2.35±1.25 vs. 5.88±3.92ng/ml,p=0.01)和 C 肽(9.14±7.36 vs. 50±42.8 µU/ml,p=0.01)水平明显较低。无意识组与其他患者在空腹测试期间的原始血糖水平无明显差异(9.4±8.2 vs. 12.2±8.2个月,P=0.28):我们描述了胰岛素瘤患者对低血糖不自知的现象。由于现有证据大多与 I 型糖尿病患者有关,因此这种现象尚未在胰岛素瘤患者中得到认可。这可能会导致更高的发病率和诊断延误。应进一步开展前瞻性评估研究,以进一步确认胰岛素瘤患者中相对较高的患病率。