青少年胰岛素瘤的模糊神经性低血糖症状伪装诊断1例。

Kelsee Halpin, Ryan McDonough, Patria Alba, Jared Halpin, Vivekanand Singh, Yun Yan
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引用次数: 8

摘要

背景:胰岛素瘤在普通人群中是一种罕见的诊断,估计每年25万人中有1人患有胰岛素瘤。这些胰岛细胞瘤的报道在儿童和青少年中更为罕见。胰岛素瘤引起的慢性低血糖通常表现为容易被忽视的神经低血糖症状,特别是在非特异性主诉常见的青少年中。这可能导致诊断延迟,并伴有长期未经治疗的低血糖和相关并发症。小儿胰岛素瘤的罕见性、表现症状的模糊性和肿瘤定位的挑战使胰岛素瘤成为临床医生真正的诊断困境。病例介绍:在本报告中,我们报告了一名15岁的女性,她去看她的初级保健提供者,抱怨间歇性的精神状态改变,包括疲劳、易怒和注意力不集中。她的门诊管理包括常规实验室检查、药物筛查、脑电图、丙戊酸起始、腹部CT扫描和内镜超声检查,有低血糖记录,但其他结果不确定。患者在初步评估后8个月因严重难治性低血糖入住三级儿童医院。获得血清临界样本并进行腹部磁共振成像(MRI),证实胰腺肿块的存在,最终确定为胰岛素瘤。她继续手术切除肿瘤,导致她的低血糖和相关症状完全解决。结论:在本报告中,我们证明了对继发于胰岛素瘤的空腹低血糖保持警惕的重要性,即使患者出现非特异性症状,如疲劳、易怒或注意力不集中。如果这些神经性低血糖疾病的主诉被忽视或误诊,具有潜在可治愈疾病的患者就会因未经治疗的严重低血糖而面临神经损伤甚至死亡的风险。
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Vague neuroglycopenic complaints camouflage diagnosis of adolescent insulinoma: a case report.

Background: Insulinoma is a rare diagnosis in the general population with estimates of 1 in 250,000 people per year. Reports of these pancreatic islet cell tumors are even more unusual in children and adolescents. Chronic hypoglycemia due to an insulinoma often presents with neuroglycopenic symptoms that can easily be overlooked, especially in adolescents where nonspecific complaints are common. This may result in delayed diagnosis with prolonged periods of untreated hypoglycemia and associated complications. The rarity of pediatric insulinoma, vagueness of presenting symptoms, and challenge of tumor localization make insulinoma a true diagnostic quandary for clinicians.

Case presentation: In this report, we present a 15-year-old female who visited her primary care provider complaining of intermittent episodes of altered mental status including fatigue, irritability, and poor concentration. Her outpatient management included routine laboratory studies, drug screening, electroencephalogram (EEG), valproic acid initiation, CT scan of the abdomen, and endoscopic ultrasound with documentation of hypoglycemia, but otherwise inconclusive results. The patient was admitted to a tertiary children's hospital with severe refractory hypoglycemia 8 months after the initial evaluation. A serum critical sample was obtained and magnetic resonance imaging (MRI) of the abdomen performed which confirmed the presence of a pancreatic mass ultimately identified as an insulinoma. She went on to have surgical resection of her tumor resulting in complete resolution of her hypoglycemia and associated symptoms.

Conclusion: Within this report we demonstrate the importance of being vigilant for fasting hypoglycemia secondary to insulinoma even when the patient presents with nonspecific symptoms such as fatigue, irritability, or problems with concentration. If these neuroglycopenic complaints are unnoticed or misdiagnosed, patients with a potentially curable disease are put at risk of neurologic injury, or even death, due to untreated severe hypoglycemia.

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