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一例由转移性涎腺肌上皮癌引起的非胰岛细胞瘤性低血糖症

A Case of Nonislet Cell Tumor Hypoglycemia Due to Metastatic Salivary Myoepithelial Carcinoma.

作者信息

Slack Margaret C, Sovich Samantha, Sachs Chana R, Martinez Dorothy, Yu Run

机构信息

Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California.

Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California.

出版信息

AACE Clin Case Rep. 2024 Jun 18;10(5):184-187. doi: 10.1016/j.aace.2024.06.002. eCollection 2024 Sep-Oct.

Abstract

BACKGROUND/OBJECTIVE: Nonislet cell tumor hypoglycemia (NICTH) is an uncommon cause of hypoglycemia due to a relative surplus of insulin-like growth factor 2 (IGF-2) or its precursor molecule. The diagnosis is confirmed by an elevated ratio of IGF-2 to insulin-like growth factor 1 (IGF-1). Myoepithelial carcinoma (MECA) is a rare and aggressive salivary gland cancer that has not been previously associated with NICTH.

CASE REPORT

A 63-year-old female with a past medical history of metastatic salivary MECA, type 2 diabetes mellitus previously on metformin, hypertension, and hypothyroidism presented to her oncologist for chemotherapy and was found to have a serum glucose of 30 mg/dL (reference: 65-99). She was admitted for further diagnostic work-up which revealed an insulin level of <1 μU/mL (reference: 3-25), C-peptide <0.5 ng/mL (reference: 1.1-4.3), IGF-1 of 15 ng/mL (reference: 41-279), and IGF-2 of 147 ng/mL (reference: 180-580) with an IGF-2:IGF-1 molar ratio of 10, consistent with NICTH. The patient's hypoglycemia unfortunately was quite resistant to treatment, requiring a combination of corticosteroids, continuous dextrose infusion, and somatostatin injections. The patient died 3 weeks after presenting with hypoglycemia.

DISCUSSION

Salivary MRCAs commonly contain pleomorphic adenoma gene 1 oncogene rearrangements which are associated with increased IGF-2 production and may predispose patients to hypoglycemia.

CONCLUSION

This case demonstrates that NICTH can be associated with metastatic salivary MECA. The hypoglycemia in this scenario is challenging to manage and is associated with poor prognosis.

摘要

背景/目的:非胰岛细胞瘤性低血糖症(NICTH)是一种罕见的低血糖病因,由胰岛素样生长因子2(IGF-2)或其前体分子相对过剩所致。通过IGF-2与胰岛素样生长因子1(IGF-1)的比值升高来确诊。肌上皮癌(MECA)是一种罕见且侵袭性强的唾液腺癌,此前未发现其与NICTH有关。

病例报告

一名63岁女性,既往有转移性唾液腺MECA病史、曾服用二甲双胍治疗的2型糖尿病史、高血压病史及甲状腺功能减退病史,因化疗就诊于肿瘤内科医生,发现其血糖为30mg/dL(参考范围:65 - 99)。她因进一步诊断检查入院,检查发现胰岛素水平<1μU/mL(参考范围:3 - 25),C肽<0.5ng/mL(参考范围:1.1 - 4.3),IGF-1为15ng/mL(参考范围:41 - 279),IGF-2为147ng/mL(参考范围:180 - 580),IGF-2:IGF-1摩尔比为10,符合NICTH。不幸的是,该患者的低血糖对治疗相当抵抗,需要联合使用皮质类固醇、持续葡萄糖输注和生长抑素注射治疗。该患者在出现低血糖3周后死亡。

讨论

唾液腺MRCAs通常含有多形性腺瘤基因1癌基因重排,这与IGF-2产生增加有关,可能使患者易患低血糖症。

结论

本病例表明NICTH可能与转移性唾液腺MECA有关。这种情况下的低血糖症治疗具有挑战性,且预后较差。

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