Literature DB >> 11402519

[A disseminated form of Langerhans histiocytosis associated with diabetes insipidus and diabetes mellitus].

I Ben Ghorbel1, M H Houman, S B'chir, S Chamakhi, M Miled.   

Abstract

INTRODUCTION: Langerhans' cell histiocytosis is a rare disorder of unknown etiology characterized by a wide clinical spectrum and varied behavior. Diabetes insipidus is a relatively common feature in Langerhans' cell histiocytosis. The presence of both diabetes insipidus and mellitus associated with histiocytosis in an adult is rare. To our knowledge, only three previous cases have been reported. EXEGESIS: We report the clinical presentation, pathologic findings and clinical progress in an adult female who had disseminated Langerhans' cell histiocytosis (hypothalamic infiltration, multifocal bone involvement) associated with both diabetes insipidus and mellitus.
CONCLUSION: The pathogenesis of diabetes mellitus in such an association will be discussed.

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Year:  2001        PMID: 11402519     DOI: 10.1016/s0248-8663(01)00373-3

Source DB:  PubMed          Journal:  Rev Med Interne        ISSN: 0248-8663            Impact factor:   0.728


  1 in total

1.  Diabetes Mellitus, Extreme Insulin Resistance, and Hypothalamic-Pituitary Langerhans Cells Histiocytosis.

Authors:  Mathilde Sollier; Marine Halbron; Jean Donadieu; Ahmed Idbaih; Fleur Cohen Aubart; Corinne Vigouroux; Martine Auclair; Olivier Bourron; Marie Bastin; Géraldine Béra; Philippe Touraine; Jacques Young; Héléna Mosbah; Agnès Hartemann; Fabrizio Andreelli; Chloé Amouyal
Journal:  Case Rep Endocrinol       Date:  2019-06-23
  1 in total

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