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Corticotropinomas account for 20% of all aggressive pituitary tumors and pituitary carcinomas and are associated with high mortality. These tumors not only cause neurovascular compromise but can also be fatal due to severe hypercortisolemia itself. Although surgery is considered the primary treatment modality, it is often partially successful or unsuccessful. Moreover, these tumors frequently recur and may be resistant to conventional treatments, including surgery and radiotherapy. Therefore, early multimodal treatment and regular follow-up are necessary. We present a case of aggressive Cushing's disease managed with combined temozolomide therapy and radiotherapy following an unsuccessful transsphenoidal surgery, resulting in significant long-term radiological and biochemical remission. In addition, etomidate infusion was administered to achieve rapid cortisol reduction, highlighting its role as a bridging therapy to other modalities in treating life-threatening and severe hypercortisolemia outside an intensive care setting.
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http://dx.doi.org/10.1177/14782715241293817 | DOI Listing |
Front Endocrinol (Lausanne)
September 2025
Department of Internal Medicine and Endocrinology, Medical University of Warsaw, Warsaw, Poland.
Isolated ectopic secretion of corticotropin-releasing hormone (CRH) is an exceedingly rare cause of Cushing's syndrome (CS), accounting for fewer than 1% of cases. Ectopic CS is an uncommon but potentially life-threatening condition that often necessitates urgent diagnostic evaluation and treatment. Hormonal testing may suggest a pituitary origin, complicating the diagnostic process.
View Article and Find Full Text PDFFront Endocrinol (Lausanne)
August 2025
Department of Hypertension, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Objective: This study aimed to investigate the risk factors associated with renal impairment among patients diagnosed with primary aldosteronism (PA).
Methods: This study enrolled 147 PA patients who were initially classified into hypokalemic (n=56) and normokalemic (n=91) groups according to serum potassium levels, followed by subgroup stratification using combined adrenal venous sampling (AVS) and computed tomography (CT) diagnostic data. For comparison, 280 patients diagnosed with essential hypertension (EH) served as the control group.
Pan Afr Med J
August 2025
Service d'Endocrinologie et Maladies Métaboliques, Centre Hospitalier Universitaire Ibn Sina, Rabat, Maroc.
Paraneoplastic Cushing's syndrome is a rare cause of ACTH-dependent Cushing's syndrome, rarely observed in young adults, and often presents a challenge in determining its etiology. We report the case of a 16-year-old female patient presenting with a severe hypercortisolism, for which no underlying cause could initially be identified. Her clinical condition worsened, leading to emergency bilateral adrenalectomy as a life-saving measure.
View Article and Find Full Text PDFBMC Endocr Disord
August 2025
Department of Endocrinology and Metabolism, Japanese Red Cross Society Kyoto Daiichi Hospital, 15-749, Honmachi, Higashiyama-ku, Kyoto, 605-0981, Japan.
Background: Cushing's syndrome (CS) during pregnancy is a rare condition associated with significant maternal and fetal complications, including hypertension, diabetes, preeclampsia, and preterm birth. Diabetes insipidus (DI) in pregnancy is a rare but often diagnosed condition, and its effective management is crucial for maintaining maternal health during pregnancy and childbirth. This case report describes the rare coexistence of DI and CS during pregnancy, highlighting the unique complexities in diagnosis and management.
View Article and Find Full Text PDFAnal Chim Acta
October 2025
Department of Laboratory Medicine, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing, 100730, China; State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College & Chines
Background: The 24-hour urinary aldosterone test offers superior stability in assessing aldosterone secretion compared to single-point plasma measurements, suggesting its potential utility as a diagnostic tool for primary aldosteronism. However, its clinical utility is hampered by labor-intensive manual urine treatment and the lack of diagnostic cut-off, with the former demonstrating considerable inter-laboratory variability. There is an urgent need for an automated assay to facilitate rapid and standardized 24-hour urinary aldosterone testing, accompanied by method-specific diagnostic cut-offs.
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