Congenital adrenal hyperplasia (CAH) represents a group of autosomal recessive disorders characterized by enzyme deficiencies thatimpair adrenal steroidogenesis, most commonly due to 21-hydroxylase deficiency. The biochemical defects in CAH translate to a spectrumof clinical consequences, which include adrenal insuffic...
M. Bobrowicz, Z. Roszkowska, J. Domański et al.· Endokrynologia Polska· 0 citations
Mild autonomous cortisol secretion (MACS) is the most frequent form of cortisol excess in patients with adrenal incidentalomas. Although it lacks the classical phenotype of overt Cushing’s syndrome, MACS is increasingly recognized as a clinically relevant condition associated with multisystem complications rather than...
G. Bluszcz, Z. Roszkowska, J. Domański et al.· Frontiers in Endocrinology· 0 citations
An intraoperative ACTH monitoring during resection of hormone-secreting neuroendocrine neoplasms remains a subject of a debate. We present the case of a 36-year-old man with clinical and biochemical features of ACTH-dependent hypercortisolism. Dynamic endocrine testing, including the high-dose dexamethasone suppression...
Agata Pokrzywa, J. Domański, Z. Roszkowska et al.· Frontiers in Endocrinology· 0 citations
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