| Literature DB >> 27241967 |
Abstract
Endogenous Cushing syndrome (CS) in pediatrics is rare; it may be caused by tumors that produce corticotropin in the pituitary gland or elsewhere, tumors that produce corticotropin-releasing hormone anywhere, and adrenocortical masses that produce cortisol. Adrenocortical cancer is a rare cause of CS in children but should be excluded first. CS in children is often caused by germline or somatic mutations with implications for patient prognosis and for their families. CS should be recognized early in children; otherwise, it can lead to significant morbidity and mortality. Patients with suspected CS should be referred to specialized clinical centers for workup. Published by Elsevier Inc.Entities:
Keywords: AIP gene; ARMC5 gene; Adrenal gland; Cyclic AMP (cAMP); GNAS1 gene; PRKAR1A gene; Pituitary gland; USP8 gene
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Year: 2016 PMID: 27241967 PMCID: PMC4889872 DOI: 10.1016/j.ecl.2016.01.006
Source DB: PubMed Journal: Endocrinol Metab Clin North Am ISSN: 0889-8529 Impact factor: 4.741