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Autor:
Silvia Einaudi, Licia Peruzzi, Federica Chiale, Enrica Abrigo, Isabella Morra, Luca Lonati, Gianpaolo Di Rosa
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 32:1193-1197
Background Pheochromocytomas (PCCs) and paragangliomas (PGLs) are known to physicians as the “great mimickers” because of their variable presentation, especially in the pediatric population. Rarely, they co-secrete other hormones. Case presentati
Publikováno v:
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
Background There is limited data on adrenal function in the early days after birth in extremely premature infants. The relationship between plasma adrenocorticotrophic (ACTH) and cortisol hormone is central to the integrity of the hypothalamic-pituit
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 31:823-827
Background Infantile hepatic haemangiomas (IHHs) produce an excess of the thyroid hormone inactivating enzyme type-3 iodothyronine deiodinase (D3), leading to rapid degradation of thyroid hormones and consumptive hypothyroidism. The L-thyroxine repla
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 29
BACKGROUND Congenital hypothyroidism (CH) is the most frequent endocrine disorder during the neonatal period, and a delay in diagnosis and treatment leads to irreversible complications. A high L-thyroxine (LT4) dose is recommended for treatment, whil