Insipid diabetes as initial presentation of Wegener´s granulomatosis

Authors

  • Lorena Narváez Ponce Sección Reumatología, Servicio de Clínica Médica. Hospital Italiano de Buenos Aires y Fundación Dr. Pedro M. Catoggio para el Progreso de la Reumatología. Instituto Universitario Escuela de Medicina, Hospital Italiano de Buenos Aires.
  • Judith Carrió Sección Reumatología, Servicio de Clínica Médica. Hospital Italiano de Buenos Aires y Fundación Dr. Pedro M. Catoggio para el Progreso de la Reumatología. Instituto Universitario Escuela de Medicina, Hospital Italiano de Buenos Aires.
  • Enrique R. Soriano Sección Reumatología, Servicio de Clínica Médica. Hospital Italiano de Buenos Aires y Fundación Dr. Pedro M. Catoggio para el Progreso de la Reumatología. Instituto Universitario Escuela de Medicina, Hospital Italiano de Buenos Aires.
  • Carlos D. Santos Sección Reumatología, Servicio de Clínica Médica. Hospital Italiano de Buenos Aires y Fundación Dr. Pedro M. Catoggio para el Progreso de la Reumatología. Instituto Universitario Escuela de Medicina, Hospital Italiano de Buenos Aires.
  • Patricia M. Imamura Sección Reumatología, Servicio de Clínica Médica. Hospital Italiano de Buenos Aires y Fundación Dr. Pedro M. Catoggio para el Progreso de la Reumatología. Instituto Universitario Escuela de Medicina, Hospital Italiano de Buenos Aires.
  • Luis J. Catoggio Sección Reumatología, Servicio de Clínica Médica. Hospital Italiano de Buenos Aires y Fundación Dr. Pedro M. Catoggio para el Progreso de la Reumatología. Instituto Universitario Escuela de Medicina, Hospital Italiano de Buenos Aires.

DOI:

https://doi.org/10.31053/1853.0605.v66.n1.23538

Keywords:

Wegener´s granulomatosis, insipid diabetes, neurologic involvement

Abstract

Wegener´s granulomatosis is a granulomatous necrotizing vasculitis which predominantly affects the respiratory tract, kidney, and less frequently other organs such as the nervous system. 
The latter may occur in up to 54% of cases and when it does it is more frequently of the peripheral nerves. We present a 19 year old woman who commenced her disease with involvement of respiratory sinuses, lungs and kidney and who developed central insipid diabetes (CID) at onset. 
The CID persisted in spite of adequate response of the other organs and systems with immunosuppresor treatment. The development of CID in the context of vasculitis should suggest this as a possible mechanism.

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References

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Published

2009-02-25

Issue

Section

Case Report

How to Cite

1.
Ponce LN, Carrió J, Soriano ER, Santos CD, Imamura PM, Catoggio LJ. Insipid diabetes as initial presentation of Wegener´s granulomatosis. Rev Fac Cien Med Univ Nac Cordoba [Internet]. 2009 Feb. 25 [cited 2024 Nov. 24];66(1):31-5. Available from: https://revistas.psi.unc.edu.ar/index.php/med/article/view/23538

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