一名两岁儿童因胰岛素瘤导致的高胰岛素血症。

JCEM case reports Pub Date : 2024-09-16 eCollection Date: 2024-09-01 DOI:10.1210/jcemcr/luae161
Lauren M Mitteer, Lisa States, Tricia Bhatti, N Scott Adzick, Katherine Lord, Diva D De León
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摘要

胰岛素瘤是一种罕见的分泌胰岛素的肿瘤,最常见于成年人。一名 26 个月大的儿童因严重低血糖症到当地急诊科就诊。初步检查结果与高胰岛素血症性低血糖一致。在长达 10 个月的时间里,医生试用了多种治疗高胰岛素血症(HI)的方法,但效果不明显。与高胰岛素血症相关的基因检测结果呈阴性。35 个月大时,患者转到本中心接受进一步治疗。她接受了多项影像学检查,结果显示她的胰腺上有一个胰岛素瘤病变。患者接受了手术治疗,切除了病灶。标本的组织病理学检查证实这是一个良性、圆形的胰岛素瘤。术后空腹检测证明患者已经痊愈,出院时无需再进行血糖监测。
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Hyperinsulinemic Hypoglycemia Due to an Insulinoma in a 2-Year-Old Child.

Insulinomas are rare insulin-secreting tumors that most commonly affect adults. A 26-month-old child presented to her local emergency department with severe hypoglycemia. Initial workup was consistent with hyperinsulinemic hypoglycemia. Over the course of 10 months, multiple therapies for hyperinsulinism (HI) were trialed without significant benefit. Genetic testing for genes associated with HI was negative. At age 35 months, the patient was transferred to our center for further treatment. She underwent several imaging tests that revealed a lesion on her pancreas concerning for an insulinoma. The patient underwent surgical intervention to enucleate the lesion. Histopathological review of the specimen confirmed a benign, well-circumscribed insulinoma. A postoperative fasting test proved the patient was cured and she was discharged without the need for further glucose monitoring.

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