Adrenal oncocytoma: a rare presentation of a benign 18 F-fluorodeoxyglucose PET avid virilising adrenal tumour. [PDF]
Lee D+11 more
europepmc +1 more source
ABSTRACT Pheochromocytoma and paraganglioma (together PPGL) are tumours with a high degree of heritability. Genetic landscape is divided into three clusters, cluster 1 (Krebs/pseudohypoxia signalling pathway), cluster 2 (kinase signalling pathway) and cluster 3 (Wnt signalling pathway).
Sakshi Jhawar+5 more
wiley +1 more source
Bidirectional Ventricular Tachycardia due to Pheochromocytoma: A Case Report. [PDF]
Li GY, Lin MX, Zhou FG, Li Q.
europepmc +1 more source
ABSTRACT Context It is well recognised there is a high prevalence of pituitary dysfunction in childhood brain tumours survivors who are treated with radiotherapy. In contrast, the potential for survivors of brain tumours arising in adulthood to develop radiotherapy‐induced hypopituitarism may be underestimated.
Darran Mc Donald+7 more
wiley +1 more source
Androgen producing oncocytic adrenocortical tumor in a 3.7-year-old female. [PDF]
Mans KD+3 more
europepmc +1 more source
[Adrenal gland neoplasms--selected aspects].
T, Przystasz, J, Lisicki
openaire +1 more source
Prevalence of Metabolic‐Associated Steatotic Liver Disease in Patients With Primary Aldosteronism
ABSTRACT Objective To assess the prevalence of metabolic associated steatotic liver disease (MASLD) in patients with primary aldosteronism (PA) compared to benign adrenal adenomas, and to evaluate the impact of hormonal excess in inducing MASLD. Design Single‐centre retrospective study. Methods Hepatic steatosis was assessed by liver/spleen (L/S) ratio
Irene Tizianel+6 more
wiley +1 more source
Metastatic Renal Cell Carcinoma Presenting a Maxillary Mucosal Lesion as a First Visible Sign of Disease: A Case Report and Review of Literature. [PDF]
Habiba U+10 more
europepmc +1 more source
Prenatal Diagnosis of Proteus Syndrome: About a Case
ABSTRACT Proteus syndrome (PS) is a rare disorder (< 1/1000000), marked by progressive overgrowth commonly impacting the skeleton, skin, adipose tissue, and central nervous system. Clinical criteria were established in 2019. PS arises from a somatic activating variation in the AKT1 gene.
Luana Giovannangeli+10 more
wiley +1 more source
Primary aldosteronism diagnosis in the intensive care unit: resistant alkalosis and hypokalemia during severe sepsis with hyperlactatemia: a case report. [PDF]
Garg Y+9 more
europepmc +1 more source