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Advances in Pediatrics

Pituitary Tumors in Children

  • Craig A. Alter
    Correspondence
    Corresponding author.
    Affiliations
    Division of Endocrinology, The Children’s Hospital of Philadelphia, 34th and Civic Center Boulevard, Philadelphia, PA 19104, USA

    Raymond and Ruth Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA
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  • Karuna V. Shekdar
    Affiliations
    Division of Radiology, The Children’s Hospital of Philadelphia, 34th and Civic Center Boulevard, Philadelphia, PA 19104, USA

    Raymond and Ruth Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA
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  • Laurie E. Cohen
    Affiliations
    Division of Endocrinology, Boston Children’s Hospital, 300 Longwood Avenue, Boston, MA 02115, USA

    Harvard Medical School, Boston, MA, USA
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      Pituitary tumors or cysts are common findings in pediatric brain scans.

      Keywords

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      References

        • Mahdi E.S.
        • Webb R.L.
        • Whitehead M.T.
        Prevalence of pituitary cysts in children using modern magnetic resonance imaging techniques.
        Pediatr Radiol. 2019; 49: 1781-1787
        • Tien R.D.
        • Kucharczyk J.
        • Bessette J.
        • et al.
        MR imaging of the pituitary gland in infants and children: changes in size, shape, and MR signal with growth and development.
        AJR Am J Roentgenol. 1992; 158: 1151-1154
        • Sari S.
        • Sari E.
        • Akgun V.
        • et al.
        Measures of pituitary gland and stalk: from neonate to adolescence.
        J Pediatr Endocrinol Metab. 2014; 27: 1071-1076
        • Gunes A.
        • Ozbal Gunes S.
        The neuroimaging features of Rathke's cleft cysts in children with endocrine-related diseases.
        Diagn Interv Radiol. 2020; 26: 61-67
        • Erfurth E.M.
        Diagnosis, background, and treatment of hypothalamic damage in craniopharyngioma.
        Neuroendocrinology. 2020; 110: 767-779
      1. Craniopharyngioma – Childhood Statistics. Available at: https://www.cancer.net/cancer-types/craniopharyngioma-childhood/statistics. Accessed April 11, 2020.

        • Muller H.L.
        • Merchant T.E.
        • Puget S.
        • et al.
        New outlook on the diagnosis, treatment and follow-up of childhood-onset craniopharyngioma.
        Nat Rev Endocrinol. 2017; 13: 299-312
        • Muller H.L.
        Management of endocrine disease: childhood-onset craniopharyngioma: state of the art of care in 2018.
        Eur J Endocrinol. 2019; 180: R159-R174
        • Gump J.M.
        • Donson A.M.
        • Birks D.K.
        • et al.
        Identification of targets for rational pharmacological therapy in childhood craniopharyngioma.
        Acta Neuropathol Commun. 2015; 3: 30
        • Muller H.L.
        The diagnosis and treatment of craniopharyngioma.
        Neuroendocrinology. 2020; 110: 753-766
        • Zoicas F.
        • Schofl C.
        Craniopharyngioma in adults.
        Front Endocrinol (Lausanne). 2012; 3: 46
        • Pascual J.M.
        • Rosdolsky M.
        • Prieto R.
        • et al.
        Jakob Erdheim (1874-1937): father of hypophyseal-duct tumors (craniopharyngiomas).
        Virchows Arch. 2015; 467: 459-469
        • Muller H.L.
        • Merchant T.E.
        • Warmuth-Metz M.
        • et al.
        Craniopharyngioma.
        Nat Rev Dis Primers. 2019; 5: 75
        • Castro-Dufourny I.
        • Carrasco R.
        • Prieto R.
        • et al.
        The infundibulo-tuberal syndrome caused by craniopharyngiomas: clinicopathological evidence from an historical French cohort (1705-1973).
        Pituitary. 2015; 18: 642-657
        • Zacharia B.E.
        • Bruce S.S.
        • Goldstein H.
        • et al.
        Incidence, treatment and survival of patients with craniopharyngioma in the surveillance, epidemiology and end results program.
        Neuro Oncol. 2012; 14: 1070-1078
        • Bao Y.
        • Pan J.
        • Qi S.T.
        • et al.
        Origin of craniopharyngiomas: implications for growth pattern, clinical characteristics, and outcomes of tumor recurrence.
        J Neurosurg. 2016; 125: 24-32
        • Pan J.
        • Qi S.
        • Liu Y.
        • et al.
        Growth patterns of craniopharyngiomas: clinical analysis of 226 patients.
        J Neurosurg Pediatr. 2015; 17: 418-433
        • Zhang N.
        • Zhou P.
        • Meng Y.
        • et al.
        A retrospective review of 34 cases of pediatric pituitary adenoma.
        Childs Nerv Syst. 2017; 33: 1961-1967
        • Russ S.
        • Shafiq I.
        Pituitary adenoma.
        StatPearls, Treasure Island (FL)2020
        • Molitch M.E.
        Nonfunctioning pituitary tumors and pituitary incidentalomas.
        Endocrinol Metab Clin North Am. 2008; 37 (xi): 151-171
        • Cristobal A.
        • Vorona G.
        • Ritter A.
        • et al.
        Pre- and postnatal MR imaging of an asymptomatic giant hypothalamic hamartoma.
        Radiol Case Rep. 2020; 15: 1250-1255
        • Siwa A.
        • Autrata R.
        • Vejmelkova K.
        • et al.
        Neurofibromatosis type 1 and optic pathway glioma.
        Cesk Slov Oftalmol. 2019; 75: 200-208
        • Robison N.J.
        • Prabhu S.P.
        • Sun P.
        • et al.
        Predictors of neoplastic disease in children with isolated pituitary stalk thickening.
        Pediatr Blood Cancer. 2013; 60: 1630-1635
        • Donadieu J.
        • Rolon M.A.
        • Pion I.
        • et al.
        Incidence of growth hormone deficiency in pediatric-onset Langerhans cell histiocytosis: efficacy and safety of growth hormone treatment.
        J Clin Endocrinol Metab. 2004; 89: 604-609
        • Di Iorgi N.
        • Allegri A.E.
        • Napoli F.
        • et al.
        Central diabetes insipidus in children and young adults: etiological diagnosis and long-term outcome of idiopathic cases.
        J Clin Endocrinol Metab. 2014; 99: 1264-1272
        • Ybarra M.
        • Hafiz R.
        • Robinson M.E.
        • et al.
        A new imaging entity consistent with partial ectopic posterior pituitary gland: report of six cases.
        Pediatr Radiol. 2020; 50: 107-115
        • Webb E.A.
        • Dattani M.T.
        Septo-optic dysplasia.
        Eur J Hum Genet. 2010; 18: 393-397
        • Lenz A.M.
        • Root A.W.
        Empty sella syndrome.
        Pediatr Endocrinol Rev. 2012; 9: 710-715
        • Herber S.M.
        • Milner R.D.G.
        Growth hormone deficiency presenting under age 2 years.
        Arch Dis Child. 1984; 59: 557-560
        • Leung A.K.C.
        • Lam J.M.
        • Leong K.F.
        Childhood Langerhans cell histiocytosis: a disease with many faces.
        World J Pediatr. 2019; 15: 536-545
        • Freda P.U.
        • Beckers A.M.
        • Katznelson L.
        • et al.
        Pituitary incidentaloma: an endocrine society clinical practice guideline.
        J Clin Endocrinol Metab. 2011; 96: 894-904
        • Thaker V.V.
        • Lage A.E.
        • Kumari G.
        • et al.
        Clinical course of nonfunctional pituitary microadenoma in children: a single-center experience.
        J Clin Endocrinol Metab. 2019; 104: 5906-5912