Case Report: ACTH- and CRH-secreting pheochromocytoma as a very rare cause of ectopic Cushing syndrome [PDF]
Ectopic adrenocorticotropic hormone (ACTH) syndrome (EAS) represents a rare clinical entity characterized by severe hypercortisolemia. Pheochromocytoma, a neuroendocrine neoplasm originating from chromaffin cells within the adrenal medulla, is itself an ...
Barbara Bromińska +7 more
doaj +2 more sources
Ectopic ACTH-syndrome is the most diagnostically challenging variant of endogenous hypercortisolism. Particularly difficult differential diagnosis of this syndrome is from Cushing's disease (CD), as currently there is no single test sufficiently ...
Larisa Konstantinovna Dzeranova +10 more
doaj +3 more sources
Metabolic complications of endogenous Cushing: patient selection for screening
Aims: this study evaluates the most common associations of symptoms and complications in patients with Cushing’s syndrome (CS) in order to choose a potential population to be screened for CS and estimates the diagnostic accuracy of first line screening ...
V V, Krylov +5 more
doaj +3 more sources
Case Report: Ectopic CRH production by adrenal adenoma as a unique cause of the ACTH-dependent Cushing’s syndrome [PDF]
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.
Agata Pokrzywa +4 more
doaj +2 more sources
Utility of gel filtration chromatography in evaluating successful resection of ectopic adrenocorticotropic hormone-producing tumor: a case report and literature review [PDF]
Ectopic adrenocorticotropic hormone (ACTH) syndrome resulting from ectopically secreting tumors poses a significant clinical challenge. Accurately identifying the tumor source and achieving curative resection are pivotal for patient prognosis; however ...
Mei Nakatsuji +11 more
doaj +2 more sources
Ectopic adrenocorticotropic secretion (EAS) is responsible for 12-17% of cases of Cushing's syndrome (CS) and covers a range of tumours, from undetectable benign lesions to widespread metastases. The syndrome is often associated with severe hypercortisolaemia, which aggravates the underlying condition.
ISIDORI, Andrea, LENZI, Andrea
openaire +7 more sources
Here, we report the first adult case of pancreatic yolk sac tumor with ectopic adrenocorticotropic hormone (ACTH) syndrome. The patient was a 27-year-old woman presenting with abdominal distension, Cushingoid features, and hyperpigmentation.
Johnny Yau Cheung Chang +12 more
doaj +1 more source
Medullary Thyroid Carcinoma with Ectopic Adrenocorticotropic Hormone Syndrome [PDF]
Ectopic adrenocorticotropic hormone (ACTH) syndrome is caused most frequently by a bronchial carcinoid tumor or by small cell lung cancer. Medullary thyroid carcinoma (MTC) is a rare etiology of ectopic ACTH syndrome.
Hong Seok Choi +11 more
doaj +1 more source
Severe Hypokalaemia, Hypertension, and Intestinal Perforation in Ectopic Adrenocorticotropic Hormone Syndrome [PDF]
Ectopic adrenocorticotropic hormone (ACTH) syndrome is a rare cause of the Cushing’s syndrome. The occurrence of the ectopic ACTH syndrome presenting with severe hypokalaemia, metabolic alkalosis, and hypertension has been highlighted in case reports ...
Tezcan Kaya +4 more
doaj +1 more source
Case Report: An Unusual Case of Ectopic ACTH Syndrome Caused by Mediastinal Paraganglioma
Ectopic adrenocorticotrophic hormone (ACTH) syndrome is not common, which is more unusual when caused by paraganglioma. We herein present a 40-year-old Chinese male who was diagnosed with ACTH-dependent Cushing’s syndrome.
Bo Li, Zhe Yan, Hui Huang
doaj +1 more source

