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Adrenal Glands DiseasesArchives

Landscape of congenital adrenal hyperplasia cases in adult endocrinology clinics of Türkiye-a nation-wide multicentre study

 Published on 19/09/2024 |  Original article (Full-text)  | Melek Eda Ertorer et al. | Endocrine 2024; 85(2): 916-25

Congenital adrenal hyperplasia (CAH) is a group of autosomal recessively inherited disorders characterized by various pathological gene variations on zone-specific enzymes that modulate steroid biosynthesis in the adrenal gland. The disorder manifests itself in a wide spectrum of clinical and biochemical...

Memory in female adolescents with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

 Published on 12/09/2024 |  Original article (Full-text)  | Tania M. Espinosa Reyes   et al. | Endocrine 2024; 85(3): 1379-86

Congenital adrenal hyperplasia (CAH) is the most common adrenal insufficiency in childhood, is caused by genetic variations affecting the enzymes involved in cortisol biosynthesis and is an autosomal recessive disorder [1]. The most common variant of CAH, 21-hydroxylase deficiency (21OHD), accounts for...

Genetic testing for familial hyperaldosteronism type 1 in Aotearoa/New Zealand

 Published on 05/09/2024 |  Original article (Full-text)  | Marianne S. Elston et al. | Internal Medicine Journal 2024; AOP: 10.1111/imj.16511

Hypertension is common, affecting around 30% of adults globally, including in Aotearoa/New Zealand (AoNZ). Hypertension is an important modifiable risk factor for cardiovascular, cerebrovascular and renal disease. The most common endocrine cause of secondary hypertension is primary aldosteronism (PA),...

Distant recurrence of non‐muscle invasive bladder cancer 8 years after initial treatment

 Published on 29/08/2024 |  Original article (Full-text)  | Mahoro Watanabe et al. | International Journal of Urology 2024; AOP: 10.1002/iju5.12775

Distant recurrence of non‐muscle invasive bladder cancer without local progression is rare. Diagnosis of this condition may be difficult when other tumor origins are clinically suspected or when the interval to recurrence is long. Although evaluation of the urinary tract is mainly recommended for...

Pitfalls in Cytological Diagnosis of Extra Adrenal Paraganglioma and Pheochromocytoma: Experience From a Tertiary Care Center

 Published on 22/08/2024 |  Original article (Full-text)  | Raktim Mukherjee et al. | Diagnostic Cytopathology 2024; AOP: 10.1002/dc.25390

Pheochromocytoma and extra‐adrenal paragangliomas are catecholamine secreting neuroendocrine tumors arising from chromaffin cells of adrenal medulla or sympathetic‐parasympathetic ganglia. These tumors are increasingly detected nowadays because of improved imaging techniques and biochemical...