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垂体柄阻断综合征合并身高过高、血液系统异常一例报告

王曦 许建萍 伍学焱

王曦, 许建萍, 伍学焱. 垂体柄阻断综合征合并身高过高、血液系统异常一例报告[J]. 协和医学杂志, 2015, 6(5): 381-383. doi: 10.3969/j.issn.1674-9081.2015.05.014
引用本文: 王曦, 许建萍, 伍学焱. 垂体柄阻断综合征合并身高过高、血液系统异常一例报告[J]. 协和医学杂志, 2015, 6(5): 381-383. doi: 10.3969/j.issn.1674-9081.2015.05.014

垂体柄阻断综合征合并身高过高、血液系统异常一例报告

doi: 10.3969/j.issn.1674-9081.2015.05.014
详细信息
    通讯作者:

    伍学焱 电话:010-69155073, E-mail:wsheyan@vip.sina.com

  • 中图分类号: R584

  • 图  1  左手骨龄相(患者为右利手)示骨皮质变薄,骨小梁稀疏,各掌骨、指骨及尺桡骨骨骺未闭合,骨龄约15岁

    图  2  鞍区磁共振平扫T1加权相(矢状位)示垂体高度约5 mm,垂体柄未见显示,垂体后叶短T1信号异位至第三脑室漏斗部

  • [1] Mehta A, Hindmarsh PC, Mehta H, et al. Congenital hypopituitarism clinical, molecular and neuroradiological correlates[J]. Clin Endocrinol (Oxf), 2009, 71:376-382. doi:  10.1111/j.1365-2265.2009.03572.x
    [2] Alatzoglou KS, Dattani MT. Genetic forms of hypopituitarism and their manifestation in the neonatal period[J]. Early Hum Dev, 2009, 85:705-712. doi:  10.1016/j.earlhumdev.2009.08.057
    [3] Fujisawa I, Kikuchi K, Nishimura K, et al. Transection of the pituitary stalk:development of an ectopic posterior lobe assessed with MR imaging[J]. Radiology, 1987, 165:487-489. doi:  10.1148/radiology.165.2.3659371
    [4] Wang Q, Hu Y, Li G, et al. Pituitary stalk interruption syndrome in 59 children:the value of MRI in assessment of pituitary functions[J]. Eur J Pediatr, 2014, 173:589-595. doi:  10.1007/s00431-013-2214-1
    [5] Wang W, Wang S, Jiang Y, et al. Relationship between pituitary stalk (PS) visibility and the severity of hormone deficiencies:PS interruption syndrome revisited[J]. Clin Endocrinol (Oxf), 2015, 83:369-376. doi:  10.1111/cen.12788
    [6] Guo Q, Yang Y, Mu Y, et al. Pituitary stalk interruption syndrome in Chinese people clinical characteristic analysis of 55 cases[J]. PLoS One, 2013, 8:e53579. doi:  10.1371/journal.pone.0053579
    [7] Andrikoula M, Sertedaki A, Andrikoula S, et al. PROP-1 gene mutations in a 63-year-old woman presenting with osteoporosis and hyperlipidaemia[J]. Hormones (Athens), 2013, 12:128-134. doi:  10.1007/BF03401294
    [8] Hess O, Khayat M, Hwa V, et al. A novel mutation in IGFALS, c.380T>C (p.L127P), associated with short stature, delayed puberty, osteopenia and hyperinsulinaemia in two siblings:insights into the roles of insulin growth factor-1(IGF1)[J]. Clin Endocrinol (Oxf), 2013, 79:838-844. doi:  10.1111/cen.12200
    [9] Irwig MS. Male hypogonadism and skeletal health[J]. Curr Opin Endocrinol Diabetes Obes, 2013, 20:517-522. doi:  10.1097/01.med.0000436185.36717.76
    [10] Laitinen EM, Hero M, Vaaralahti K, et al. Bone mineral density, body composition and bone turnover in patients with congenital hypogonadotropic hypogonadism[J]. Int J Androl, 2012, 35:534-540. doi:  10.1111/j.1365-2605.2011.01237.x
    [11] Gokalp D, Tuzcu A, Bahceci M, et al. Sheehan's syndrome as a rare cause of anaemia secondary to hypopituitarism[J]. Ann Hematol, 2009, 88:405-410. doi:  10.1007/s00277-008-0607-4
    [12] Bowles KM, Turner GE, Wimperis JZ. Resolution of chronic severe refractory thrombocytopenia after treatment of hypothyroidism[J]. J Clin Pathol, 2004, 57:995-996. doi:  10.1136/jcp.2004.016543
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  • 被引次数: 0
出版历程
  • 收稿日期:  2015-07-17
  • 刊出日期:  2015-09-30

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