Endocrine manifestations of Erdheim-Chester disease (a distinct form of histiocytosis)

Erdheim-Chester disease (ECD) is a disorder of unclear aetiology, characterized by exuberant histiocyte proliferation and a variable clinical course. We report the case of a woman with multi-organ involvement secondary to ECD. Central diabetes insipidus (CDI), hyperprolactinaemia, gonadotropin insuf...

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Veröffentlicht in:	Journal of internal medicine 1998-12, Vol.244 (6), p.529-535
Hauptverfasser:	TRITOS, N. A, WEINRIB, S, KAYE, T. B
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Diabetes Insipidus - etiology Endocrine System Diseases - etiology Female Gonadotropins - deficiency Histiocytosis - complications Histiocytosis - physiopathology Humans Hyperprolactinemia - etiology Hypothalamo-Hypophyseal System - physiopathology Insulin-Like Growth Factor I - analysis Medical sciences Middle Aged Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis
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