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儿童鞍区肿瘤术后垂体功能减退合并非酒精性脂肪性肝病的临床特征分析

杜婷婷 姚辉 陈晓红 罗杰 杨禄红 丰利芳 陈晓倩 胡曼 罗娟

引用本文:
Citation:

儿童鞍区肿瘤术后垂体功能减退合并非酒精性脂肪性肝病的临床特征分析

DOI: 10.3969/j.issn.1001-5256.2023.06.013
基金项目: 

中华国际医学交流基金会 (Z-2019-41-2101-01)

伦理学声明:本研究方案于2022年5月10日经由武汉儿童医院伦理委员会审批,批号:2022R039-F01。
利益冲突声明:本文不存在任何利益冲突。
作者贡献声明:杜婷婷撰写论文;杜婷婷、姚辉、陈晓红对研究的思路及设计有关键贡献;罗杰、杨禄红、丰利芳、陈晓倩、胡曼、罗娟参与研究数据的获取和解释过程。
详细信息
    通信作者:

    姚辉,yaohui1024@sina.com (ORCID: 0000-0002-1878-0012)

Clinical features of hypopituitarism with nonalcoholic fatty liver disease after sellar tumor surgery in children

Research funding: 

China International Medical Foundation (Z-2019-41-2101-01)

More Information
  • 摘要:   目的  总结儿童鞍区肿瘤术后垂体功能减退合并非酒精性脂肪性肝病(NAFLD)的临床特征,探索儿童垂体功能减退与NAFLD之间的临床联系。  方法  回顾性分析2017年1月—2021年12月于华中科技大学同济医学院附属武汉儿童医院规律随访的鞍区肿瘤术后垂体功能减退出现NAFLD的患儿临床资料,分析临床特点。  结果  共32例规律随访且临床资料完整的鞍区肿瘤术后患者,其中10例(31.25%)出现NAFLD,其中男5例,女5例,9例为颅咽管瘤,均手术治疗,1例为生殖细胞瘤,局部放射治疗。10例患儿诊断垂体功能减退时的中位年龄为8.4(6.2~9.8)岁;诊断NAFLD的中位年龄为11.9(8.7~12.6)岁。从诊断垂体功能减退至诊断NAFLD的中位年数为2.0(1.4~4.0)年。诊断NAFLD时,10例患者均为肥胖,BMI较诊断垂体功能减退时平均增加(7.26±4.25)kg/m2;10例患者空腹血糖均正常,平均为(4.67±0.55)mmol/L,平均空腹胰岛素水平为(25.40±5.93)μIU/mL;胰岛素抵抗指数(HOMA-IR)平均为(5.26±1.29);9例患者有高甘油三酯血症,1例患者甘油三酯升高,平均为(3.08±1.09)mmol/L;6例患者有高胆固醇血症,平均为(5.67±1.25)mmol/L;8例患者有高低密度脂蛋白胆固醇血症,平均为(3.97±1.27)mmol/L。2例患者诊断NAFLD予重组人生长激素联合二甲双胍治疗,治疗后患儿BMI、HOMA-IR及甘油三酯均较治疗前下降,总胆固醇、低密度脂蛋白胆固醇均降至正常范围。  结论  鞍区肿瘤术后患儿可出现体质量增加及垂体功能减退,继而出现胰岛素抵抗及血脂异常,从而导致NAFLD的发生。对这类患儿应进行体质量管理和积极的垂体激素替代治疗,并予以常规的脂肪肝相关筛查和管理。

     

  • 表  1  10例患者诊断垂体功能减退时的临床特征

    Table  1.   Clinical features of the 10 patients when they diagnosed with hypopituitarism

    项目 病例1 病例2 病例3 病例4 病例5 病例6 病例7 病例8 病例9 病例10 正常范围
    性别
    年龄(岁) 6 8.1 11 6.3 11.5 9.4 9 8.6 7.8 5.8
    鞍区肿瘤 颅咽管瘤 颅咽管瘤 生殖细胞瘤 颅咽管瘤 颅咽管瘤 颅咽管瘤 颅咽管瘤 颅咽管瘤 颅咽管瘤 颅咽管瘤
    身高(cm) 108 132 154 114 143 146 112 124 119 112
    身高SDS -2.0 0.3 1.0 -1.0 -0.8 1.7 -3.8 -1.5 -1.4 -0.8
    体质量(kg) 20.0 43.5 49.0 22.5 41.5 48.5 14.0 29.0 24.0 19.0
    BMI(kg/m2) 17.1 (超重) 25 (肥胖) 20.6 (超重) 17.5 (超重) 20.2 (正常) 22.8 (肥胖) 11.2 (消瘦) 18.9 (超重) 16.8 (正常) 15.1 (正常)
    TSH(μIU/mL) 0.02 0.04 3.61 0.33 1.80 0.71 0.02 0.75 2.80 0.92 0.5~6.2
    FT3(pmol/L) 7.36 2.89 3.20 2.66 2.82 1.96 2.74 3.96 2.08 1.98 5.2~8.6
    FT4(pmol/L) 3.42 10.96 6.54 7.19 5.65 9.15 9.85 6.47 9.43 9.48 12~22
    ACTH(pg/mL) <10 <10 23.5 14.0 13.2 <10 <10 <10 <10 <10 0~46
    8am皮质醇(nmol/L) <13.79 26.50 24.04 <13.80 <13.80 25.60 16.34 14.56 18.70 32.0 >82.8
    生长激素峰值(ng/mL) <0.05 <0.05 <0.65 <0.05 <0.20 <0.05 <0.46 <0.05 <0.05 <0.05 >10
    IGF-1(ng/mL) 31.3 59.2 98.3 33.1 75.6 57.4 <25 40.0 <25 69.5
      注:TSH,促甲状腺素;FT3,游离三碘甲状腺原氨酸;FT4,游离甲状腺素;ACTH,促肾上腺皮质素;生长激素峰值为胰岛素和盐酸可乐定片联合激发。
    下载: 导出CSV

    表  2  10例患者诊断NAFLD时的临床特征

    Table  2.   Clinical features of the 10 patients when they diagnosed with NAFLD

    项目 病例1 病例2 病例3 病例4 病例5 病例6 病例7 病例8 病例9 病例10 正常范围
    性别
    年龄(岁) 10.0 12.4 12.8 7.8 12.5 11.3 13.8 12.6 9.0 7.9
    年龄间隔(年) 4.0 4.3 1.8 1.5 1.0 1.9 4.8 4.0 1.2 2.1
    身高(cm) 126.9 149.0 160.0 118.5 147.0 151.6 133.0 140.0 123.0 120.3
    身高SDS -2.1 -0.5 0.7 -1.8 -1.1 0.5 -4.3 -2 -1.9 -1.5
    体质量(kg) 50.0 60.5 67.0 31.0 52.0 65.5 45.5 54.5 32.5 34.0
    BMI(kg/m2) 31.3 (肥胖) 27.3 (肥胖) 26.2 (肥胖) 22 (肥胖) 24 (肥胖) 28.4 (肥胖) 25.7 (肥胖) 27.8 (肥胖) 21.5 (肥胖) 23.5 (肥胖)
    BMI变化(kg/m2) 14.2 2.3 5.6 4.5 3.8 5.6 14.6 8.9 4.7 8.4
    GLU(mmol/L) 4.03 5.20 4.70 5.92 4.84 4.42 4.13 4.56 4.39 4.60 3.9~6.1
    INS(μIU/mL) 19.09 23.52 32.52 24.93 17.84 33.41 31.40 23.27 29.38 18.66 3~25
    HOMA-IR 3.4 5.4 6.8 6.6 3.8 6.6 5.8 4.7 5.7 3.8 <3
    ALT(U/L) 42 42 40 22 32 48 10 166 34 18 7~45
    AST(U/L) 24 36 32 27 24 44 15 109 45 21 10~50
    TC(mmol/L) 6.74 3.74 4.92 6.52 6.19 7.79 5.49 6.16 4.01 5.14 2.8~4.8
    TG(mmol/L) 3.46 3.70 1.99 2.14 2.12 5.03 4.04 3.74 3.02 1.62 0.32~1.46
    LDL-C(mmol/L) 5.19 2.06 3.69 5.08 4.31 5.65 3.54 4.09 2.74 3.39 1.55~2.86
    下载: 导出CSV

    表  3  病例3 rhGH治疗前后各项指标的变化

    Table  3.   Variations of observation indexes before and after rhGH treatment of case 3

    项目 治疗前 治疗3个月 治疗6个月 治疗9个月 治疗1年 正常范围
    年龄(岁) 13.4 14.4
    身高(cm) 161.3 163.5
    体质量(kg) 65.0 62.0
    BMI(kg/m2) 25.0 23.3
    IGF-1(ng/mL) 109 336 336 232 230 537~715
    GLU(mmol/L) 4.23 4.40 4.36 4.30 4.59 3.9~6.1
    INS(μIU/mL) 37.41 33.56 29.80 28.90 26.96 3~25
    HOMA-IR 7.0 6.5 5.7 5.5 5.5 <3
    TC(mmol/L) 5.57 4.28 4.16 2.8~4.8
    TG(mmol/L) 2.60 1.38 1.84 0.32~1.46
    LDL-C(mmol/L) 3.53 2.76 2.69 1.55~2.86
    ALT(U/L) 17 24 8 7~45
    AST(U/L) 19 21 12 10~50
    肝脏超声 脂肪肝(中-重度) 轻度脂肪肝
    下载: 导出CSV

    表  4  病例10 rhGH治疗前后各项指标的变化

    Table  4.   Variations of observation indexes before and after rhGH treatment of case 10

    项目 治疗前 治疗3个月 治疗6个月 治疗9个月 治疗1年 正常范围
    年龄(岁) 7.9 8.9
    身高(cm) 120.3 127.7
    体质量(kg) 34.0 32.0
    BMI(kg/m2) 23.5 19.6
    IGF-1(ng/mL) 116 268 213 227 201 236~419
    GLU(mmol/L) 4.49 4.15 4.61 4.39 3.58 3.9~6.1
    INS(μIU/mL) 18.66 2.80 10.40 2.73 1.95 3~25
    HOMA-IR 3.7 0.5 2.1 0.6 0.3 <3
    TC(mmol/L) 5.14 3.50 4.24 4.21 3.92 2.8~4.8
    TG(mmol/L) 1.62 1.0 0.80 0.62 0.57 0.32~1.46
    LDL-C(mmol/L) 3.39 2.07 2.19 2.19 2.41 1.55~2.86
    HDL-C(mmol/L) 1.19 1.13 1.74 1.77 1.34 7~45
    ALT(U/L) 18 9 8 10 10~50
    AST(U/L) 21 20 14 20
    肝脏超声 轻度脂肪肝 正常
      注:HDL-C,高密度脂蛋白胆固醇。
    下载: 导出CSV
  • [1] HONG JW, KIM JY, KIM YE, et al. Metabolic parameters and nonalcoholic fatty liver disease in hypopituitary men[J]. Horm Metab Res, 2011, 43(1): 48-54. DOI: 10.1055/s-0030-1265217.
    [2] KANG SJ, KWON A, JUNG MK, et al. High prevalence of nonalcoholic fatty liver disease among adolescents and young adults with hypopituitarism due to growth hormone deficiency[J]. Endocr Pract, 2021, 27(11): 1149-1155. DOI: 10.1016/j.eprac.2021.06.003.
    [3] HOFFMANN A, BOOTSVELD K, GEBHARDT U, et al. Nonalcoholic fatty liver disease and fatigue in long-term survivors of childhood-onset craniopharyngioma[J]. Eur J Endocrinol, 2015, 173(3): 389-397. DOI: 10.1530/EJE-15-0422.
    [4] ADAMS LA, FELDSTEIN A, LINDOR KD, et al. Nonalcoholic fatty liver disease among patients with hypothalamic and pituitary dysfunction[J]. Hepatology, 2004, 39(4): 909-914. DOI: 10.1002/hep.20140.
    [5] ALABSAWY E, SERRY Y, KOTHA S, et al. Hepatopulmonary syndrome as the first and only manifestation of cirrhosis in a patient with hypopituitarism[J]. BMJ Case Rep, 2021, 14(9): e244805. DOI: 10.1136/bcr-2021-244805.
    [6] MAZERKINA NA, SAVATEEV AN, GORELYSHEV SK, et al. Hepatopulmonary syndrome: a rare manifestation of cirrhosis in patient with diencephalic obesity and nonalcoholic fatty liver disease after surgery for craniopharyngioma[J]. Probl Endokrinol (Mosk), 2021, 67(5): 58-66. DOI: 10.14341/probl12723.
    [7] TORII N, ICHIHARA A, MIZUGUCHI Y, et al. Hormone-replacement therapy for hepatopulmonary syndrome and NASH associated with hypopituitarism[J]. Intern Med, 2018, 57(12): 1741-1745. DOI: 10.2169/internalmedicine.0027-17.
    [8] JUNG D, SEO GH, KIM YM, et al. Hepatopulmonary syndrome caused by hypothalamic obesity and nonalcoholic fatty liver disease after surgery for craniopharyngioma: a case report[J]. Ann Pediatr Endocrinol Metab, 2018, 23(1): 51-55. DOI: 10.6065/apem.2018.23.1.51.
    [9] JONAS MM, KRAWCZUK LE, KIM HB, et al. Rapid recurrence of nonalcoholic fatty liver disease after transplantation in a child with hypopituitarism and hepatopulmonary syndrome[J]. Liver Transpl, 2005, 11(1): 108-110. DOI: 10.1002/lt.20332.
    [10] JUSTINO H, SANDERS K, MCLIN VA. Rapid progression from hepatopulmonary syndrome to portopulmonary hypertension in an adolescent female with hypopituitarism[J]. J Pediatr Gastroenterol Nutr, 2010, 50(3): 334-336. DOI: 10.1097/MPG.0b013e3181a1c496.
    [11] FUJIO A, KAWAGISHI N, ECHIZENYA T, et al. Long-term survival with growth hormone replacement after liver transplantation of pediatric nonalcoholic steatohepatitis complicating acquired hypopituitarism[J]. Tohoku J Exp Med, 2015, 235(1): 61-67. DOI: 10.1620/tjem.235.61.
    [12] Subspecialty Group of Endocrine Genetic Metabolism, Society of Pediatrics, Chinese Medical Association; Subspecialty Group of Gastroenterology, Society of Pediatrics, Chinese Medical Association; Professional Committee on Adolescent Medicine, Chinese Pediatric Society, Chinese Medical Association, et al. Expert consensus on the diagnosis and treatment of nonalcoholic fatty liver disease in children[J]. Chin J Pract Pediatr, 2018, 33(7): 487-492. DOI: 10.19538/j.ek2018070602.

    中华医学会儿科学分会内分泌遗传代谢学组, 中华医学会儿科学分会消化学组, 中华医学会儿科学分会青春期医学专业委员会, 等. 儿童非酒精性脂肪肝病诊断与治疗专家共识[J]. 中国实用儿科杂志, 2018, 33(7): 487-492. DOI: 10.19538/j.ek2018070602.
    [13] LI H, JI CY, ZONG XN, et al. Body mass index growth carves for Chinese children and adolescents aged 0 to 18 years[J]. Chin J Pediatr, 2009, 47(7): 493-498. DOI: 10.3760/cma.j.issn.0578-1310.2009.07.004.

    李辉, 季成叶, 宗心南, 等. 中国0~18岁儿童、青少年体块指数的生长曲线[J]. 中华儿科杂志, 2009, 47(7): 493-498. DOI: 10.3760/cma.j.issn.0578-1310.2009.07.004.
    [14] National Health and Family Planning Commission of the People's Republic of China. WS/T 586-2018 Screening for overweight and obesity in school-age children and adolescent[S]. Beijing: Standards Press of China, 2018.

    中华人民共和国国家卫生和计划生育委员会. WS/T 586-2018学龄儿童青少年超重和肥胖筛查[S]. 北京: 中国标准出版社, 2018.
    [15] Subspecialty Group of Insulin Resistance, Chinese Diabetes Society, Chinese Medical Association (in preparation). Expert guidance on methods and application of insulin resistance assessment[J]. Chin J Diabetes Mellitus, 2018, 10(6): 377-385. DOI: 10.3760/cma.j.issn.1674-5809.2018.06.001.

    中华医学会糖尿病学分会胰岛素抵抗学组(筹). 胰岛素抵抗评估方法和应用的专家指导意见[J]. 中华糖尿病杂志, 2018, 10(6): 377-385. DOI: 10.3760/cma.j.issn.1674-5809.2018.06.001.
    [16] YIN J, LI M, XU L, et al. Insulin resistance determined by Homeostasis Model Assessment (HOMA) and associations with metabolic syndrome among Chinese children and teenagers[J]. Diabetol Metab Syndr, 2013, 5(1): 71. DOI: 10.1186/1758-5996-5-71.
    [17] The Editorial Board, Chinese Journal of Pediatrics; Subspecialty Group of Child Care, Chinese Pediatric Society, Chinese Medical Association; Subspecialty Group of Cardiology, Chinese Pediatric Society, Chinese Medical Association, et al. Expert consensus on the prevention and treatment of dyslipidemia in children and adolescents[J]. Chin J Pediatr, 2009, 47(6): 426-428. DOI: 10.3760/cma.j.issn.0578-1310.2009.06.007.

    《中华儿科杂志》编辑委员会, 中华医学会儿科学分会儿童保健学组, 中华医学会儿科学分会心血管学组, 等. 儿童青少年血脂异常防治专家共识[J]. 中华儿科杂志, 2009, 47(6): 426-428. DOI: 10.3760/cma.j.issn.0578-1310.2009.06.007.
    [18] STEFAN N, HÄRING HU, CUSI K. Non-alcoholic fatty liver disease: causes, diagnosis, cardiometabolic consequences, and treatment strategies[J]. Lancet Diabetes Endocrinol, 2019, 7(4): 313-324. DOI: 10.1016/S2213-8587(18)30154-2.
    [19] MANN JP, VALENTI L, SCORLETTI E, et al. Nonalcoholic fatty liver disease in children[J]. Semin Liver Dis, 2018, 38(1): 1-13. DOI: 10.1055/s-0038-1627456.
    [20] WANG CE, XU WT, GONG J, et al. Research progress in the treatment of nonalcoholic fatty liver disease[J]. Clin J Med Offic, 2022, 50(9): 897-899, 903. DOI: 10.16680/j.1671-3826.2022.09.06.

    王彩娥, 许文涛, 宫建, 等. 非酒精性脂肪性肝病治疗研究进展[J]. 临床军医杂志, 2022, 50(9): 897-899, 903. DOI: 10.16680/j.1671-3826.2022.09.06.
    [21] DU TT, YAO H, LI YK, et al. Hepatopulmonary syndrome after craniopharyngioma operation in children: A case report[J]. J Clin Hepatol, 2022, 38(7): 1620-1625. DOI: 10.3969/j.issn.1001-5256.2022.07.030.

    杜婷婷, 姚辉, 李亚坤, 等. 儿童颅咽管瘤术后出现肝肺综合征1例报告[J]. 临床肝胆病杂志, 2022, 38(7): 1620-1625. DOI: 10.3969/j.issn.1001-5256.2022.07.030.
    [22] KHAN MJ, HUMAYUN KN, DONALDSON M, et al. Longitudinal changes in body mass index in children with craniopharyngioma[J]. Horm Res Paediatr, 2014, 82(6): 372-379. DOI: 10.1159/000368798.
    [23] HOCHBERG I, HOCHBERG Z. Hypothalamic obesity[J]. Endocr Dev, 2010, 17: 185-196. DOI: 10.1159/000262539.
    [24] ABUZZAHAB MJ, ROTH CL, SHOEMAKER AH. Hypothalamic obesity: Prologue and promise[J]. Horm Res Paediatr, 2019, 91(2): 128-136. DOI: 10.1159/000496564.
    [25] FUJII H, KAWADA N, JSG-NAFLD JSGON. The role of insulin resistance and diabetes in nonalcoholic fatty liver disease[J]. Int J Mol Sci, 2020, 21(11): 3863. DOI: 10.3390/ijms21113863.
    [26] MØLLER N, JØRGENSEN JO. Effects of growth hormone on glucose, lipid, and protein metabolism in human subjects[J]. Endocr Rev, 2009, 30(2): 152-177. DOI: 10.1210/er.2008-0027.
    [27] WIJNEN M, van den HEUVEL-EIBRINK MM, JANSSEN J, et al. Very long-term sequelae of craniopharyngioma[J]. Eur J Endocrinol, 2017, 176(6): 755-767. DOI: 10.1530/EJE-17-0044.
    [28] HUANG Q, XU H, WANG X, et al. Relationship between growth hormone deficiency and nonalcoholic fatty liver disease in patients with pituitary stalk interruption syndrome[J]. Clin Endocrinol (Oxf), 2022, 97(5): 612-621. DOI: 10.1111/cen.14732.
    [29] NISHIZAWA H, IGUCHI G, MURAWAKI A, et al. Nonalcoholic fatty liver disease in adult hypopituitary patients with GH deficiency and the impact of GH replacement therapy[J]. Eur J Endocrinol, 2012, 167(1): 67-74. DOI: 10.1530/EJE-12-0252.
    [30] The Subspecialty Gorup of Endocrinologic, Hereditary and Metabolic Disease, The Society of Pediatrics, Chinese Medical Association; The Editorial Board, Chinese Journal of Pediatrics. Expert consensus on the diagnosis and management of growth hormone deficiency during the transition period[J]. Chin J Pediatr, 2020, 58(6): 455-460. DOI: 10.3760/cma.j.cn112140-20200314-00237.

    中华医学会儿科学分会内分泌遗传代谢学组, 中华儿科杂志编辑委员会. 过渡期生长激素缺乏症诊断及治疗专家共识[J]. 中华儿科杂志, 2020, 58(6): 455-460. DOI: 10.3760/cma.j.cn112140-20200314-00237.
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