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在恶性神经内分泌肿瘤中开始使用生长抑素类似物后隐匿性胰岛素瘤的发现

Unmasking insulinoma following commencement of somatostatin analogues in malignant neuroendocrine tumours.

作者信息

Gamage Isuru, Boehm Emma, Ghosh Gaurav, Kong Grace, Michael Michael, Wong HuiLi, Piercey Oliver, Sachithanandan Nirupa

机构信息

Department of Internal Medicine, Peter MacCallum Cancer Centre, Melbourne, Australia.

ENETS Centre of Excellence, Peter MacCallum Cancer Centre, Melbourne, Australia.

出版信息

Endocr Oncol. 2025 Jul 19;5(1):e250005. doi: 10.1530/EO-25-0005. eCollection 2025 Jan.

Abstract

OBJECTIVE

Somatostatin analogues (SSA) are used in the management of patients with metastatic gastroenteropancreatic neuroendocrine tumours (GEP-NET) to control hormone secretion and tumour growth. SSA can paradoxically worsen or unmask hypoglycaemia in patients with insulinoma by inhibiting counter-regulatory hormones such as glucagon and growth hormone.

DESIGN AND METHODS

We present two cases of SSA use in patients with initially presumed non-functioning GEP-NET unmasking insulinoma. We review the use of SSA in GEP-NET and the management of refractory hypoglycaemia in metastatic insulinoma.

RESULTS

A 62-year-old female with metastatic grade 2 GEP-NET was commenced on monthly lanreotide 10 weeks after diagnosis. She presented 1 week following the second dose with refractory hypoglycaemia and inappropriate hyperinsulinism, requiring inpatient dextrose infusion. SSA was stopped; however, she remained dextrose dependent despite the addition of diazoxide and dexamethasone. Peptide receptor radionuclide therapy (PRRT) with Lu-DOTA-Octreotate was given, resulting in resolution of hypoglycaemia after two cycles. The second case is a 57-year-old female with metastatic grade 2 GEP-NET. Four months post commencement of lanreotide, she presented with radiological disease progression and symptomatic hypoglycaemia. A 72 h fast confirmed hyperinsulinaemic hypoglycaemia. SSA was stopped. A trial of diazoxide was not tolerated, and a prednisolone trial was ineffective. The patient underwent inpatient PRRT with euglycaemia achieved shortly afterwards.

CONCLUSIONS

SSA can unmask hypoglycaemia secondary to insulinoma. Detection of new-onset hypoglycaemia requires careful clinical vigilance when commencing SSA in patients with GEP-NET initially presumed to be non-functional. Hypoglycaemia from metastatic insulinoma requires multidisciplinary management incorporating nutritional, medical and oncologic therapy. PRRT can be effective in managing refractory hypoglycaemia.

LEARNING POINTS

SSA use can unmask insulinoma in a NET presumed to be non-functional.SSA can paradoxically worsen hypoglycaemia in insulinoma due to suppression of counter-regulatory hormones.There are currently no biomarkers in routine clinical use to predict which patients will experience a worsening of hypoglycaemia after SSA initiation. Detection of new-onset hypoglycaemia requires clinical vigilance and education of patients to report symptoms early to enable prompt investigation and management.Symptomatic hypoglycaemia in metastatic insulinoma is challenging to manage and requires a multidisciplinary approach considering diet, medical therapy and urgent initiation or escalation of oncologic therapy.PRRT is a safe and effective strategy to achieve hormonal and oncologic control in metastatic insulinoma. Caution should be practised regarding flare of insulin release, and inpatient administration with expert endocrinology, nuclear medicine and oncology input should be considered.

摘要

目的

生长抑素类似物(SSA)用于治疗转移性胃肠胰神经内分泌肿瘤(GEP-NET)患者,以控制激素分泌和肿瘤生长。然而,SSA可通过抑制胰高血糖素和生长激素等反调节激素,反常地加重或暴露胰岛素瘤患者的低血糖症状。

设计与方法

我们报告了2例最初被推测为无功能GEP-NET的患者在使用SSA后暴露胰岛素瘤的病例。我们回顾了SSA在GEP-NET中的应用以及转移性胰岛素瘤难治性低血糖的治疗。

结果

一名62岁转移性2级GEP-NET女性患者在确诊后10周开始每月注射兰瑞肽。在第二次注射后1周,她出现难治性低血糖和不适当的高胰岛素血症,需要住院静脉输注葡萄糖。停用了SSA;然而,尽管加用了二氮嗪和地塞米松,她仍依赖葡萄糖。给予镥[177Lu]奥曲肽肽受体放射性核素治疗(PRRT),两个周期后低血糖症状缓解。第二例是一名57岁转移性2级GEP-NET女性患者。在开始使用兰瑞肽4个月后,她出现影像学疾病进展和症状性低血糖。72小时禁食证实为高胰岛素血症性低血糖。停用了SSA。二氮嗪试验未耐受,泼尼松龙试验无效。该患者接受了住院PRRT治疗,随后很快实现了血糖正常。

结论

SSA可暴露继发于胰岛素瘤的低血糖症状。对于最初被认为无功能的GEP-NET患者,在开始使用SSA时,检测新发低血糖需要临床密切监测。转移性胰岛素瘤所致低血糖需要多学科管理,包括营养、药物和肿瘤治疗。PRRT可有效治疗难治性低血糖。

学习要点

使用SSA可使被认为无功能的神经内分泌肿瘤暴露胰岛素瘤。由于反调节激素的抑制,SSA可反常地加重胰岛素瘤患者的低血糖症状。目前常规临床使用中没有生物标志物可预测哪些患者在开始使用SSA后会出现低血糖恶化。检测新发低血糖需要临床监测,并对患者进行教育,使其尽早报告症状,以便及时进行检查和处理。转移性胰岛素瘤的症状性低血糖治疗具有挑战性,需要多学科方法,考虑饮食、药物治疗以及紧急启动或加强肿瘤治疗。PRRT是在转移性胰岛素瘤中实现激素和肿瘤控制的安全有效策略。应注意胰岛素释放的激增,可考虑在住院期间给予治疗,并由内分泌学、核医学和肿瘤学专家提供支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f65/12281627/d89f72612e61/EO-25-0005fig1.jpg

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