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diabetes insipidus/céphalée
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Headaches, diabetes insipidus, and hyperprolactinemia in a woman with an enlarged pituitary gland.
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Headaches, impaired mentation, diabetes insipidus and exophthalmosis in a 50 year old man.
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Complications of diabetes insipidus: the significance headache.
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A case of Rathke's cleft cyst presenting with diabetes insipidus.
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Rathke's cleft cysts (RCCs) are considered to arise from the remnants of Rathke's pouch, an invagination of the stomodeum. They are classically described as benign epithelium lined intrasellar cysts containing mucoid material, and also found in 2-33% of routine autopsy series. The most common
A case of Rathke's Cleft Cyst inflammation presenting with diabetes insipidus.
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Rathke's Cleft Cyst (RCC), which is located at the intrasellar region, is considered to be the distended remnants of Rathke's pouch, an invagination of the stomodeum. Lined with columnar or cuboidal epithelium of ectodermal origin, RCC usually contains mucoid material and it is found in 13-22% of
Diabetes insipidus as a presenting manifestation of Rathke's cleft cyst.
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Rathke's cleft cysts (RCC) are cystic sellar and suprasellar lesions derived from remnants of Rathke's pouch, lined by cuboidal or columnar epithelium. RCC are usually asymptomatic but can present with headache, visual impairment, panhypopituitarism and hypothalamic dysfunction. Diabetes Insipidus
Atherosclerosis, aortic stenosis and sudden onset central diabetes insipidus.
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The majority of cases of central diabetes insipidus are still pathogenetically unclear (idiopathic). Atherosclerotic cholesterol emboli might be partly responsible for some of these idiopathic cases. A 54-year-old woman with known aortic valve stenosis and a history of a transitory ischemic attack
Diabetes insipidus as a consequence of neurologic involvement in Behcet's syndrome.
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OBJECTIVE
To describe a case of central diabetes insipidus that was associated with Behçet's syndrome.
METHODS
We present a case report, including clinical, laboratory, and radiologic data. The pertinent literature is reviewed relative to diabetes insipidus and Behçet's syndrome, and a discussion
[Diabetes insipidus revealing pituitary metastasis of bronchial carcinoma].
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Pituitary metastasis are rare but represent an important differential diagnosis of intrasellar tumorous syndromes. We report one case of intrasellar metastasis of a bronchial adenocarcinoma in a 50 year old woman. Clinical syndrome associated a tumorous syndrome (cephalalgia, bitemporal hemianopsia)
Clinical presentation and outcome of children with central diabetes insipidus associated with a self-limited or transient pituitary stalk thickening, diagnosed as infundibuloneurohypophysitis.
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OBJECTIVE
Despite lymphocytic or autoimmune infundibuloneurohypophysitis (INH) is an increasingly recognized aetiology in children with central diabetes insipidus (CDI); clinical data on epidemiology (clinical evolution, predisposing factors, complications), diagnosis and management of this entity
Hypopituitarism associated with transient diabetes insipidus followed by an episode of painless thyroiditis in a young man.
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A 16-year-old male complained of a headache and a high fever followed by polyuria. The endocrinological studies showed he had hypopituitarism and central diabetes insipidus, and magnetic resonance imaging (MRI) revealed a pituitary mass. Diabetes insipidus gradually improved and hydrocortisone
Idiopathic giant cell granulomatous hypophysitis with hypopituitarism, right abducens nerve paresis and masked diabetes insipidus.
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A 38-year-old man presented with headache, fever, and double vision associated with right abducens nerve paresis. He had neither nuchal rigidity nor visual field defect. Laboratory data revealed elevated erythrocyte sedimentation rate (ESR), eosinophilia, and lymphocytic pleocytosis in the
[A Case of Central Diabetes Insipidus That Was Caused by Pituitary Metastasis of Lung Adenocarcinoma and Was Controlled by Radiation Therapy].
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BACKGROUND
Pituitary metastasis of lung cancer is rare; however, it often causes diabetes insipidus. Although the majority of such patients are treated with radiation therapy, it remains unclear whether diabetes insipidus can be controlled by radiation therapy.
METHODS
A 72-year-old man was admitted
An unusual case of central diabetes insipidus & hyperglycemic hyperosmolar state following cardiorespiratory arrest.
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BACKGROUND
We are describing an unusual case of severe hyperglycemia and hypernatremia, resistant to treatment.
METHODS
A thirty year old female with adenocarcinoma of rectum was admitted with increasing lethargy, headache and drowsiness. She deteriorated rapidly and had cardiac arrest, following
Neurogenic diabetes insipidus: management with dDAVP (1-desamino-8-D arginine vasopressin).
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We used dDAVP, the 1-desamino-8-D arginine analogue of arginine vasopressin with high antidiuretic and low vasopressor potency, to treat 29 patients with neurogenic diabetes insipidus for up to 22 months. Intranasal dDAVP, 2.5 to 15 microgram twice daily, provided excellent control in most patients.
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