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A rare case of hyponatremia from a hypothalamic lesion in a patient with multiple sclerosis.
Sabatino, Joseph J; Werner, J Kent; Newsome, Scott D.
Afiliação
  • Sabatino JJ; Johns Hopkins University, Baltimore, USA.
  • Werner JK; Johns Hopkins University, Baltimore, USA.
  • Newsome SD; Johns Hopkins University, Baltimore, USA snewsom2@jhmi.edu.
Mult Scler ; 21(5): 662-5, 2015 Apr.
Article em En | MEDLINE | ID: mdl-25139944
ABSTRACT
The syndrome of inappropriate antidiuretic hormone secretion (SIADH) can occur from a variety of neurologic and systemic processes; however, it has rarely been seen in multiple sclerosis (MS). We report a case of SIADH in a patient with MS and compare it with previously reported English-only cases. A 32-year-old woman experienced generalized fatigue followed by confusion and was found to have profound hyponatremia. Her work-up demonstrated SIADH secondary to a discrete enhancing hypothalamic lesion. Despite the seldom occurrence of SIADH in MS, hypothalamic lesions are more common than appreciated and should be considered in patients presenting with hyponatremia or endocrinopathy symptoms.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiponatremia / Doenças Hipotalâmicas / Síndrome de Secreção Inadequada de HAD / Esclerose Múltipla Tipo de estudo: Etiology_studies Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiponatremia / Doenças Hipotalâmicas / Síndrome de Secreção Inadequada de HAD / Esclerose Múltipla Tipo de estudo: Etiology_studies Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article