Objective: To summarize the clinical features and therapeutic outcomes of patients with hyperinsulinemic hypoglycemia (HH) auxiliarily diagnosed by 18F-DOPA positron emission tomography (PET) CT scanning. Methods: The clinical data of 123 patients who were diagnosed with hyperinsulinemic hypoglycemia by comprehensive clinical diagnostic procedures in the Department of Pediatric Endocrinology and Inherited Metabolic Diseases, Children's Hospital of Fudan University between January 2016 and December 2020 were retrospectively analyzed. Clinical data such as gender, age of onset, province, concurrent serum insulin level measured during hypoglycemia, lesion type of pancreas by 18F-DOPA-PET CT scanning, genetic test results, and treatment were collected successively. The clinical features and therapeutic outcomes were compared between patients with focal and diffuse pancreatic lesions. T test, Rank sum test, and χ² test were used for comparison between groups. Results: A total of 123 patients with hyperinsulinemic hypoglycemia (72 males and 51 females), whose average age of onset was 3 days (ranging from 1 day to 4 860 days), were recruited from 24 provinces. The concurrent serum insulin level was 7.1 (0.4-303.0) mU/L during hypoglycemia. 18F-DOPA-PET CT scanning identified focal lesions in 25.2% (31/123) and diffuse lesions in 74.8% (92/123) of the patients; 64.2% (79/123) of the HH cases were found to have pathogenic gene variants, in which 88.6% (70/79) were found to have KATP channel related genes (61 in ABCC8 and 9 in KCNJ11 mutations). Thirty-seven patients (17 focal and 20 diffuse) received surgical treatment with a success rate of 67.6% (25/37). The effective rate of diazoxide for children with diffuse type was significantly higher than that of children with focal group (28.3% (26/92) vs. 9.7% (3/31), χ²=10.31, P=0.001). Conclusions: 18F-DOPA-PET CT scan can improve the success rate of surgery. Comprehensive diagnosis of the etiology of hyperinsulinemic hypoglycemia by genetic analysis and 18F-DOPA-PET CT scanning can result in better treatment and prognosis.
目的: 总结经18氟-多巴正电子发射断层扫描CT(18F-DOPA-PET CT)辅助诊断的高胰岛素血症性低血糖(HH)患儿的临床特征和治疗转归。 方法: 回顾性分析2016年1月至2020年12月复旦大学附属儿科医院内分泌遗传代谢科采用综合临床诊断流程诊断的123例HH患儿的临床资料,依次收集患儿的性别、发病年龄等一般情况,低血糖时同步测定的血清胰岛素水平,18F-DOPA-PET CT胰腺扫描的病灶类型,基因检测结果,治疗等临床资料。比较胰腺局灶型和弥漫型两组不同类型病灶患儿的临床特征和治疗转归。组间比较采用t检验、秩和检验和χ²检验。 结果: 123例HH患儿(男72例、女51例)发病年龄为3(1~4 860)日龄,分别来自24个省份,低血糖时同步血清胰岛素水平7.1(0.4~303.0)mU/L。18F-DOPA-PET CT扫描显示25.2%(31/123)为局灶型病变,74.8%(92/123)为弥漫型病变。64.2%(79/123)的HH患儿发现相关基因致病性变异,其中88.6%(70/79)为KATP相关通道基因(61例ABCC8基因致病性变异,9例KCNJ11基因致病性变异)。37例(17例局灶型、20例弥漫型)接受了手术治疗,手术成功率为67.6%(25/37)。弥漫型患儿二氮嗪治疗有效率显著高于局灶型患儿[28.3%(26/92)比9.7%(3/31),χ²=10.31,P=0.001]。 结论: 18F-DOPA-PET CT扫描能提高手术成功率。遗传学分析联合18F-DOPA-PET CT扫描对HH患儿进行全面的病因诊断将有助于更好地治疗和预后。.