Abstract
Cushing's disease (CD) is the commonest form of ACTH-dependent Cushing's syndrome and is a rare clinical diagnosis in paediatric and adolescent patients. CD is caused by an ACTH-secreting pituitary corticotroph adenoma and is associated with significant morbidity in children; therefore, early diagnosis and treatment are critical for optimal therapeutic outcome. This review highlights the key clinical and biochemical features of paediatric CD and appraises current practices in diagnosis and management. A close liaison with adult endocrinology colleagues, particularly, for interpretation of investigations and definition of therapeutic strategy is strongly advised.
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CITATION STYLE
Storr, H. L., & Savage, M. O. (2015, July 1). Management of endocrine disease: Paediatric Cushing’s disease. European Journal of Endocrinology. BioScientifica Ltd. https://doi.org/10.1530/EJE-15-0013
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