Halpin Kelsee, McDonough Ryan, Alba Patria, Halpin Jared, Singh Vivekanand, Yan Yun
Division of Endocrinology and Diabetes, Children's Mercy Hospital, 2401 Gillham Rd, Kansas City, MO 64108 USA.
Department of Radiology, Saint Luke's Hospital, 4401 Wornall Rd, Kansas City, MO 64111 USA.
Int J Pediatr Endocrinol. 2016;2016:14. doi: 10.1186/s13633-016-0032-8. Epub 2016 Jul 29.
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.
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.
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.
胰岛素瘤在普通人群中是一种罕见的诊断,估计每年每25万人中会有1例。这些胰岛细胞瘤在儿童和青少年中的报道更为罕见。胰岛素瘤导致的慢性低血糖常伴有神经低血糖症状,很容易被忽视,尤其是在青少年中,非特异性症状很常见。这可能导致诊断延迟,低血糖长期未得到治疗并引发相关并发症。小儿胰岛素瘤的罕见性、症状表现的模糊性以及肿瘤定位的挑战性,使胰岛素瘤成为临床医生真正的诊断难题。
在本报告中,我们介绍了一名15岁女性,她因间歇性精神状态改变(包括疲劳、易怒和注意力不集中)就诊于初级保健医生。她的门诊治疗包括常规实验室检查、药物筛查、脑电图(EEG)、开始使用丙戊酸、腹部CT扫描以及内镜超声检查,并记录了低血糖情况,但结果均无定论。在初次评估8个月后,该患者因严重难治性低血糖入住一家三级儿童医院。采集了血清关键样本并进行了腹部磁共振成像(MRI)检查,证实存在胰腺肿块,最终确诊为胰岛素瘤。她随后接受了肿瘤手术切除,低血糖及相关症状完全缓解。
在本报告中,我们证明了即使患者表现出疲劳、易怒或注意力不集中等非特异性症状,也要警惕胰岛素瘤继发的空腹低血糖的重要性。如果这些神经低血糖症状未被注意到或误诊,患有潜在可治愈疾病的患者会因严重低血糖未得到治疗而面临神经损伤甚至死亡的风险。