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胰腺神经内分泌肿瘤——非糖尿病性严重低血糖的诊断陷阱:文献综述与病例报告

Pancreatic Neuroendocrine Tumors-Diagnostic Pitfalls of Non-Diabetic Severe Hypoglycemia: Literature Review and Case Report.

作者信息

Popa Simona Georgiana, Golli Andreea Loredana, Matei Cristina Florentina, Sonei Alexandra Nicoleta, Vere Cristin, Cimpeanu Radu, Munteanu Marian, Munteanu Alexandru

机构信息

Department of Diabetes, Nutrition and Metabolic Diseases, University of Medicine and Pharmacy, 200349 Craiova, Romania.

Department of Public Health and Healthcare Management, University of Medicine and Pharmacy, 200349 Craiova, Romania.

出版信息

Diagnostics (Basel). 2025 Jan 31;15(3):337. doi: 10.3390/diagnostics15030337.

DOI:10.3390/diagnostics15030337
PMID:39941267
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11816404/
Abstract

: Hypoglycemia in the case of persons without diabetes is a rare event, being usually, initially misinterpreted based on the symptoms that can mimic various diseases, especially of a neuro-psychiatric nature. In the case of the identification of insulin-mediated hypoglycemia, the evaluation of pancreatic neuroendocrine tumors, which represent the most common and worrisome causes of non-diabetic insulin-mediated hypoglycemia, must be considered. : We present the case of a 57-year-old patient, hospitalized for a history of approximately one month of recurrent episodes of symptoms suggestive for severe hypoglycemia. The biological evaluation performed during an episode of hypoglycemia showed a plasma glucose value of 44 mg/dL, insulinemia 16.3 µU/mL, C peptide 3.72 ng/mL, HbA1c 4.99%, absence of urinary ketone bodies and anti-insulin antibodies <0.03 U/mL. The CT and MRI examination showed a 15.3/15 mm rounded tumor in the pancreatic corporeo-caudal region. The pancreatic tumor formation was enucleated and the histopathological and immunohistochemical analysis confirmed the diagnosis of the pancreatic neuroendocrine tumor with a positive reaction for chromogranin A, synaptophysin and insulin, without malignancy features (Ki 67 positive in 1% of the tumor cells). The postoperative evolution was favorable, without episodes of hypoglycemia, the fasting insulinemia one day after surgery being 4.1 µU/mL and HbA1c at three weeks postoperatively being 5.51%. : The management of patients with hyperinsulinemic hypoglycemia secondary to insulinoma involves multidisciplinary collaboration with an important role in recognizing symptoms suggestive of hypoglycemia in a person without diabetes, initiating biological and imaging evaluation, establishing the optimal therapeutic option and histopathological confirmation.

摘要

对于非糖尿病患者而言,低血糖是一种罕见事件,通常一开始会基于可能类似各种疾病(尤其是神经精神性疾病)的症状而被误诊。在确诊胰岛素介导的低血糖时,必须考虑对胰腺神经内分泌肿瘤进行评估,因为这类肿瘤是导致非糖尿病性胰岛素介导低血糖最常见且最令人担忧的原因。

我们报告一例57岁患者,因约一个月来反复出现提示严重低血糖的症状而住院。在一次低血糖发作期间进行的生物学评估显示,血糖值为44mg/dL,胰岛素水平为16.3µU/mL,C肽为3.72ng/mL,糖化血红蛋白(HbA1c)为4.99%,尿酮体阴性,抗胰岛素抗体<0.03U/mL。CT和MRI检查显示在胰体尾区域有一个15.3/15mm的圆形肿瘤。将胰腺肿瘤切除,组织病理学和免疫组织化学分析证实为胰腺神经内分泌肿瘤,嗜铬粒蛋白A、突触素和胰岛素呈阳性反应,无恶性特征(Ki 67在1%的肿瘤细胞中呈阳性)。术后恢复良好,未再出现低血糖发作,术后一天的空腹胰岛素水平为4.1µU/mL,术后三周的糖化血红蛋白为5.51%。

对于胰岛素瘤继发的高胰岛素血症性低血糖患者的管理,需要多学科协作,这在识别非糖尿病患者提示低血糖的症状、启动生物学和影像学评估、确定最佳治疗方案以及组织病理学确诊方面发挥着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e0/11816404/16a2fc2d5c14/diagnostics-15-00337-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e0/11816404/6c769ff28394/diagnostics-15-00337-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e0/11816404/16a2fc2d5c14/diagnostics-15-00337-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e0/11816404/6c769ff28394/diagnostics-15-00337-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e0/11816404/16a2fc2d5c14/diagnostics-15-00337-g002.jpg

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Genetic disorders and insulinoma/glucagonoma.遗传性疾病与胰岛素瘤/胰高血糖素瘤。
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Transformation of pancreatic nonfunctioning neuroendocrine tumor into metastatic insulinoma: A rare case report.胰腺无功能神经内分泌肿瘤转化为转移性胰岛素瘤:一例罕见病例报告。
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J Clin Endocrinol Metab. 2024 Mar 15;109(4):1109-1118. doi: 10.1210/clinem/dgad641.
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Investigation and Causes of Spontaneous (Non-Diabetic) Hypoglycaemia in Adults: Pitfalls to Avoid.成人自发性(非糖尿病性)低血糖症的调查与病因:需避免的陷阱
Diagnostics (Basel). 2023 Oct 22;13(20):3275. doi: 10.3390/diagnostics13203275.
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