Zhang M Y, Ni J W, Ge J J, Guan Y H, Pei Z, Sun C J, Wu J, Xu Z R, Yang L, Luo F H, Cheng R Q
Department of Pediatric Endocrinology and Inherited Metabolic Diseases, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai 201102, China.
PET Center, Huashan Hospital of Fudan University, Shanghai 200235, China.
Zhonghua Er Ke Za Zhi. 2021 Oct 2;59(10):853-858. doi: 10.3760/cma.j.cn112140-20210417-00326.
To summarize the clinical features and therapeutic outcomes of patients with hyperinsulinemic hypoglycemia (HH) auxiliarily diagnosed by F-DOPA positron emission tomography (PET) CT scanning. 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 F-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. 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. F-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 K 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) 9.7% (3/31), χ²=10.31, =0.001). F-DOPA-PET CT scan can improve the success rate of surgery. Comprehensive diagnosis of the etiology of hyperinsulinemic hypoglycemia by genetic analysis and F-DOPA-PET CT scanning can result in better treatment and prognosis.
总结通过F-DOPA正电子发射断层扫描(PET)CT辅助诊断的高胰岛素血症性低血糖症(HH)患者的临床特征和治疗结果。回顾性分析2016年1月至2020年12月在复旦大学附属儿科医院小儿内分泌与遗传代谢病科通过综合临床诊断程序诊断为高胰岛素血症性低血糖症的123例患者的临床资料。依次收集性别、发病年龄、省份、低血糖发作时同步检测的血清胰岛素水平、F-DOPA-PET CT扫描的胰腺病变类型、基因检测结果及治疗等临床资料。比较胰腺局灶性病变和弥漫性病变患者的临床特征及治疗结果。采用t检验、秩和检验及χ²检验进行组间比较。共纳入123例高胰岛素血症性低血糖症患者(男72例,女51例),平均发病年龄3天(范围1天至4860天),来自24个省份。低血糖发作时同步血清胰岛素水平为7.1(0.4~303.0)mU/L。F-DOPA-PET CT扫描显示25.2%(31/123)的患者为局灶性病变,74.8%(92/123)的患者为弥漫性病变;64.2%(79/123)的HH病例存在致病基因变异,其中88.6%(70/79)存在钾通道相关基因(ABCC8突变61例,KCNJ11突变9例)。37例患者(局灶性17例,弥漫性20例)接受手术治疗,成功率为67.6%(25/37)。二氮嗪治疗弥漫型患儿的有效率显著高于局灶型患儿(28.3%(26/92)对9.7%(3/31),χ² = 10.31,P = 0.001)。F-DOPA-PET CT扫描可提高手术成功率。通过基因分析和F-DOPA-PET CT扫描对高胰岛素血症性低血糖症病因进行综合诊断可获得更好的治疗及预后。