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Non-endocrine hyperaldosteronism. When hormones are supporting players.
Endocrinol Diabetes Nutr (Engl Ed)
November 2022
OSI Bilbao-Basurto, Osakidetza, Unidad de Genética Clínica, Hospital Universitario Basurto, Bilbao, Spain.
Adrenal disorders in pregnancy, labour and postpartum - an overview.
J Obstet Gynaecol
August 2020
Department of Obstetrics and Gynaecology, Azra Naheed Medical College, Lahore, Pakistan.
Adrenal disorders may manifest during pregnancy for the first time, or present from before pregnancy as either undiagnosed or diagnosed and treated. They may present as hormonal hypofunction or hyperfunction, or with mass effects or other non-endocrine effects. Adrenal disorders such as Cushing's syndrome, Addison's disease, pheochromocytoma, primary hyper-aldosteronism and adreno-cortical carcinoma are rare in pregnancy.
View Article and Find Full Text PDFA novel case of myxoid variant of adrenocortical carcinoma in a patient with multiple endocrine neoplasia type 1.
Endocr J
August 2019
Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan.
Adrenocortical carcinoma (ACC) is a rare malignancy arising from adrenocortical parenchymal cells. Myxoid ACC is one of the newly identified, rare, but important histological variants of ACC, characterized by the presence of abundant extracellular Alcian Blue-positive myxoid material. Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant cancer predisposition syndrome, and the incidence of ACC in MEN1 patients has been reported to be between 1.
View Article and Find Full Text PDFA rare case of primary hyperparathyroidism associated with primary aldosteronism, Hürthle cell thyroid cancer and meningioma.
J Korean Med Sci
May 2012
Department of Internal Medicine, Eulji University School of Medicine, Seoul, Korea.
Multiple endocrine neoplasia type 1 (MEN1) syndrome includes varying combinations of endocrine and non-endocrine tumors. There are also a considerable number of atypical MEN1 syndrome. In this case, a 68-yr-old woman was referred to the Department of Endocrinology for hypercalcemia.
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