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Emergence of Pituitary Adenoma in a Child during Surveillance: Clinical Challenges and the Family Members' View in an AIP Mutation-Positive Family.

Pedro MarquesSayka BarryAmy RonaldsonArla OgilvieHelen L StorrPeter J GoadsbyMichael PowellMary N DangHarvinder S ChahalJane EvansonAjith V KumarJoan GrieveMarta Korbonits
Published in: International journal of endocrinology (2018)
Out of the 14 members harbouring germline AIP mutations in this kindred, 5 have pituitary adenoma. Affected members had different features and courses of disease. Bulky pituitary and not fully suppressed GH on OGTT can be challenging in the evaluation of females in teenage years. Multiple pituitary adenomas with different secretory profiles may arise in the pituitary of these patients. Small, stable NFPAs can be present in mutation carriers, similar to incidentalomas in the general population. Genetic screening and baseline review, with follow-up of younger subjects, are recommended in AIP mutation-positive families.
Keyphrases
  • growth hormone
  • end stage renal disease
  • newly diagnosed
  • ejection fraction
  • chronic kidney disease
  • prognostic factors
  • dna methylation
  • patient reported outcomes