Cushing’s Disease in a 7-Month-Old Girl due to a Tumor Producing Adrenocorticotropic Hormone and Thyreotropin-Secreting Hormone
Autor: | G. Schackert, C. Bonk, T. Pinzer, S. B. Sobottka, J. Koy, J.V. List, A. Huebner |
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Jazyk: | angličtina |
Rok vydání: | 1999 |
Předmět: |
Adenoma
Pathology medicine.medical_specialty Pituitary gland endocrine system endocrine system diseases Thyrotropin Adrenocorticotropic hormone Pituitary neoplasm Hypophysenadenom Adrenocorticotropin ACTH Thyreoidea-stimulierendes Hormon TSH Cushing-Syndrom Neurochirurgie Cushing syndrome Adrenocorticotropic Hormone Thyroid-stimulating hormone GTP-Binding Proteins Pituitary adenoma Internal medicine medicine Humans Pituitary Neoplasms ddc:610 Cushing Syndrome business.industry Pituitary adenoma Adrenocorticotropic hormone Thyreotropin-secreting hormone Cushing’s disease Cushing’s syndrome Neurosurgery Infant General Medicine Cushing's disease medicine.disease Magnetic Resonance Imaging Endocrinology medicine.anatomical_structure Pediatrics Perinatology and Child Health Female Surgery Neurology (clinical) business hormones hormone substitutes and hormone antagonists |
Zdroj: | Pediatr Neurosurg 1999;31:7–11, ISSN: 1016-2291 |
Popis: | 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-geförderten) Allianz- bzw. Nationallizenz frei zugänglich. |
Databáze: | OpenAIRE |
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