Literature DB >> 15067246

[Central diabetes insipidus with Behçet disease. A case report].

K Khiari1, L Cherif, I Hadj Ali, S Turki, Y Lakhoua, N Ben Abdallah, H Ben Maïz.   

Abstract

Vasculitis with central diabetes insipidus is a rare condition which must be recognized for an appropriate management. We report a case of Behçet disease with central diabetes insipidus. A forty seven year old men presented recurring oral and genital ulcers, skin lesions, polyarthralgia. Two years later, he showed right uveitis and central diabetes insipidus without dysfunction of the pituitary gland. Computed tomographic scan showed normal neurohypophysis and pituitary gland. Later on, he presented hemiplegia. The cerebral computed tomographic scan showed hypodense lesions. Central diabetes insipidus should not be systematically searched because it is a rare feature of the Behçet disease.

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Year:  2003        PMID: 15067246

Source DB:  PubMed          Journal:  Ann Endocrinol (Paris)        ISSN: 0003-4266            Impact factor:   2.478


  2 in total

1.  Wegener's granulomatosis complicated by central diabetes insipidus and peripheral neutrophy with normal pituitary in a patient.

Authors:  Jing Xue; Huiying Wang; Huaxiang Wu; Qiaofei Jin
Journal:  Rheumatol Int       Date:  2009-01-27       Impact factor: 2.631

2.  Behcet's Disease and Endocrine System.

Authors:  Onur Ozhan; Kerem Sezer
Journal:  Patholog Res Int       Date:  2011-12-15
  2 in total

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