Correlation between responsiveness to CRH stimulation test in Cushing's disease patients and USP8 mutational status

2019 ◽  
Author(s):  
Adriana Albani ◽  
Luis Perez-Rivas ◽  
Michael Buchfelder ◽  
Jurgen Honegger ◽  
Gunter Stalla ◽  
...  
1995 ◽  
Vol 45 (5) ◽  
pp. 407-412
Author(s):  
DAISUKE KANDA ◽  
NORIYUKI SATO ◽  
YOSHITO TANAKA ◽  
TAKEHIKO UCHIDA ◽  
ICHIRO DOI ◽  
...  

1974 ◽  
Vol 76 (4) ◽  
pp. 712-718 ◽  
Author(s):  
Mogens Blichert-Toft ◽  
Lotte Hummer ◽  
Harriet Dige-Petersen

ABSTRACT In patients with untreated Cushing's disease decreased thyroid function has been demonstrated by several investigators. An inhibiting effect of glucocorticosteroids on the release of thyrotrophin seems to be the cause. In the treated patient with remission of the disease the pituitary-thyroid function has not been studied in detail. The question is, if the hypofunction proved in the untreated state might persist in the treated patient. This might be anticipated from both clinical and experimental studies. In the present study the pituitary-thyroid function has been determined after total adrenalectomy followed by remission in 14 patients with Cushing's disease. All patients were replaced adequately with cortisone acetate post-operatively as estimated by excretion of cortisol in urine. Levels of serum thyroxine, thyroxine-binding globulin, and serum thyrotrophin were measured. In addition, tracer studies were performed. The 131I-uptake in the thyroid gland and plasma protein-bound radioiodine were determined. After thyrotrophin-stimulation test, the thyroxine reserve and the rise in 131I-uptake in the gland were measured. TRH-stimulation test was performed to determine the TSH-reserve. A normal pituitary-thyroid function and a normal pituitary and thyroid reserve were demonstrated. In the conclusion it can be said that decreased pituitary-thyroid function or reserve has not been found in the Cushing-patient subjected to adrenalectomy followed by remission. Thus, thyroid replacement therapy has not to be considered, when an adequate replacement therapy is planned after total adrenalectomy.


Author(s):  
Liliana Fonseca ◽  
Diana Borges Duarte ◽  
Joana Freitas ◽  
Maria João Oliveira ◽  
Isabel Ribeiro ◽  
...  

Abstract Objectives Pituitary apoplexy is a rare complication of Cushing’s disease (CD), especially in the paediatric age and even more rarely it can occur following anterior pituitary stimulation tests. Case presentation We report a case of a 14-year-old girl who was admitted to our Hospital for evaluation of a possible Cushing’s syndrome (CS). Her symptoms and initial laboratory tests were suggestive of CD. Magnetic resonance imaging (MRI) revealed a microadenoma of the pituitary gland. As part of her evaluation she was submitted to a corticotropin-releasing hormone (CRH) stimulation test. Two and a half months later the patient was re-evaluated and presented with both clinical improvement of CS, biochemical resolution of hypercortisolism and tumour size reduction in the MRI, also evidencing a haemorrhagic component favouring the diagnosis of pituitary apoplexy after CRH stimulation test. The patient denied any episodes of severe headache, nausea, vomiting or visual changes. Conclusions To our knowledge, the authors report the first case of a pituitary apoplexy after a CRH stimulation test in the paediatric age.


Author(s):  
Wasita Warachit Parksook ◽  
Thachanun Porntharukchareon ◽  
Sarat Sunthornyothin

2018 ◽  
Vol 89 (4) ◽  
pp. 454-458 ◽  
Author(s):  
Adriana Albani ◽  
Luis G. Pérez-Rivas ◽  
Christina Dimopoulou ◽  
Stephanie Zopp ◽  
Paula Colón-Bolea ◽  
...  

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