We present the case of a 7-month-old baby with Cushing’s disease due to an adrenocorticotropic hormone (ACTH)-secreting pituitary adenoma combined with cells producing thyreotropin-secreting hormone (TSH). In MRI scans, a contrast-enhancing lesion was seen inside the pituitary fossa, and it extended into the suprasellar region. On the assumption of a pituitary adenoma, surgery was performed. Corresponding with biochemical findings, histopathological evaluation revealed an ACTH- and TSH-producing tumor. Genetic analysis did not demonstrate an alteration at codon 201 (Arg) and 227 (Glu). To our knowledge, this is the first case described in a child of this age.Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderte...
Cushing syndrome is rare in infancy and usually due to an adrenocortical tumor (ACT). We report an i...
Pituitary adenomas (PA) are benign well-differentiated tumors, with monoclonal development from the ...
Here, we report the first adult case of pancreatic yolk sac tumor with ectopic adrenocorticotropic h...
We present the case of a 7-month-old baby with Cushing’s disease due to an adrenocorticotropic hormo...
We report the case of a 12-month-old girl presenting with diabetes insipidus and Cushing s disease. ...
CASE REPORT: Adrenocorticotropic hormone (ACTH)-secreting pituitary adenoma is extremely rare. Only ...
Ectopic adrenocorticotrophic hormone (ACTH) secretion is a rare cause of Cushing syndrome in paediat...
Pituicytoma is a tumor extremely rare in childhood, with only 4 cases reported in literature. It is ...
Adrenocortical tumors (ACTs) causing Cushing’s syndrome are extremely rare in children and adolescen...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
ACTH-dependent Cushing’s syndrome results from excessive ACTH secretion from a pituitary gland adeno...
Pituitary adenoma is a rare neoplasm in childhood, with prolactin and adrenocorticotropic hormone (A...
Ectopic ACTH syndrome (EAS) is extremely rare in the pediatric age group. Sarcomatous tumors causing...
Primary Pigmented Nodular Adrenocortical Disease (PPNAD) is a rare form of bilateral adrenocortical ...
Cushing’s disease represents 60–70% of all cases of Cushing’s syndrome, presenting with a constellat...
Cushing syndrome is rare in infancy and usually due to an adrenocortical tumor (ACT). We report an i...
Pituitary adenomas (PA) are benign well-differentiated tumors, with monoclonal development from the ...
Here, we report the first adult case of pancreatic yolk sac tumor with ectopic adrenocorticotropic h...
We present the case of a 7-month-old baby with Cushing’s disease due to an adrenocorticotropic hormo...
We report the case of a 12-month-old girl presenting with diabetes insipidus and Cushing s disease. ...
CASE REPORT: Adrenocorticotropic hormone (ACTH)-secreting pituitary adenoma is extremely rare. Only ...
Ectopic adrenocorticotrophic hormone (ACTH) secretion is a rare cause of Cushing syndrome in paediat...
Pituicytoma is a tumor extremely rare in childhood, with only 4 cases reported in literature. It is ...
Adrenocortical tumors (ACTs) causing Cushing’s syndrome are extremely rare in children and adolescen...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
ACTH-dependent Cushing’s syndrome results from excessive ACTH secretion from a pituitary gland adeno...
Pituitary adenoma is a rare neoplasm in childhood, with prolactin and adrenocorticotropic hormone (A...
Ectopic ACTH syndrome (EAS) is extremely rare in the pediatric age group. Sarcomatous tumors causing...
Primary Pigmented Nodular Adrenocortical Disease (PPNAD) is a rare form of bilateral adrenocortical ...
Cushing’s disease represents 60–70% of all cases of Cushing’s syndrome, presenting with a constellat...
Cushing syndrome is rare in infancy and usually due to an adrenocortical tumor (ACT). We report an i...
Pituitary adenomas (PA) are benign well-differentiated tumors, with monoclonal development from the ...
Here, we report the first adult case of pancreatic yolk sac tumor with ectopic adrenocorticotropic h...