scholarly journals Pseudotumor cerebri during Cushing's disease treatment with ketoconazole

2011 ◽  
Vol 55 (4) ◽  
pp. 284-287 ◽  
Author(s):  
Fabiola Costenaro ◽  
Ticiana C. Rodrigues ◽  
Nelson P. Ferreira ◽  
Tiago G. da Costa ◽  
Tiago Schuch ◽  
...  

Benign intracranial hypertension (Pseudotumor cerebri) has been described as related to the reduction in steroid levels in Cushing's disease (CD), especially after surgical remission. Ketoconazole is a common and effective adjuvant therapy for hypercortisolism, but the major concern is liver enzyme dysfunction. We describe here the case of a 12-year old girl with CD who developed benign intracranial hypertension during treatment with ketoconazole. She presented headache, vomiting, a black spot on her right temporal visual field, and signs of elevated intracranial pressure. Pituitary image was normal on magnetic resonance image (MRI), and all symptoms improved after treatment with acetazolamide. We call attention to the diagnosis of this disorder in CD patients, especially children on ketoconazole treatment, because it could be confounded with adrenal insufficiency and lead to definitive severe visual impairment.

BMJ ◽  
1980 ◽  
Vol 281 (6233) ◽  
pp. 113-113 ◽  
Author(s):  
P K Newman ◽  
M Snow ◽  
P Hudgson

Neurosurgery ◽  
1983 ◽  
Vol 13 (2) ◽  
pp. 195-198 ◽  
Author(s):  
Mark N. Weissman ◽  
Larry K. Page ◽  
Raphael L. Bejar

Abstract A 7-year-old girl presented with the physical and endocrinological stigmata of Cushing's disease. An adrenocorticotropic hormone (ACTH)-producing pituitary microadenoma was excised. Three weeks after trans-sphenoidal adenomectomy, the patient developed benign intracranial hypertension. Although ACTH levels had decreased to normal, the serum cortisol had fallen to subnormal levels. The child responded to exogenous steroid therapy, which was gradually tapered and discontinued after 5 months. Normal pituitary and adrenal functions persist 2 years later.


1994 ◽  
Vol 70 (820) ◽  
pp. 115-117 ◽  
Author(s):  
V. J. Parfitt ◽  
J. C. Dearlove ◽  
D. Savage ◽  
H. B. Griffith ◽  
M. Hartog

Neurosurgery ◽  
1981 ◽  
Vol 8 (6) ◽  
pp. 699-702 ◽  
Author(s):  
Neil A. Martin ◽  
John Linfoot ◽  
Charles B. Wilson

abstract A patient with Cushing's disease developed intracranial hypertension 1 month after the removal of an adrenocorticotropic hormone-secreting pituitary adenoma. A computed tomographic scan demonstrated normal ventricles and no intracranial mass, establishing the diagnosis of pseudotumor cerebri. The elevated intracranial pressure was apparently consequent to an abrupt reduction in circulating corticosteroids. The development of pseudotumor cerebri after the correction of endogenous hypercortisolism has not been reported previously. This potential complication of the surgical treatment of Cushing's disease can be managed with prompt recognition and appropriate treatment of the syndrome.


2018 ◽  
Vol 62 (1) ◽  
pp. 87-105 ◽  
Author(s):  
Márcio Carlos Machado ◽  
Maria Candida Barisson Vilares Fragoso ◽  
Ayrton Custódio Moreira ◽  
César Luiz Boguszewski ◽  
Leonardo Vieira ◽  
...  

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