Cerebral Salt Wasting Syndrome in Children: One Case and Review of the Literature
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چکیده
منابع مشابه
Cerebral Salt Wasting Syndrome in Children: One Case and Review of the Literature
Background: Cerebral Salt Wasting Syndrome (CSWS) refers to the process of intracranial lesions, sodium salt loss by hypothalamus-renal pathway and caused clinical manifestations syndrome of high urinary sodium, hyponatremia, hypovolemia. The clinical manifestations and laboratory are similar to syndrome of inappropriate antidiuretic hormone secretion (SIADH). It is easy to be misdiagnosed. Cas...
متن کاملCerebral salt wasting syndrome: review.
Hyponatremia is the most frequent electrolyte disorder in critically neurological patients. Cerebral salt wasting syndrome (CSW) is defined as a renal loss of sodium during intracranial disease leading to hyponatremia and a decrease in extracellular fluid volume. The pathogenesis of this disorder is still not completely understood. Sympathetic responses as well as some natriuretic factors play ...
متن کاملCerebral salt wasting syndrome: a case report.
A case of hyponatraemia associated with subarachnoid haemorrhage is presented. The provisional diagnosis of an inappropriate antidiuresis was made and treatment with fluid restriction was instituted. However the patient continued to deteriorate as the diuresis continued and the hyponatraemia worsened, resulting in hypovolaema. The salt wasting syndrome was subsequently diagnosed and saline and ...
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Cerebral salt wasting in tuberculous meningitis: Two cases and review of the literature. Case Report.
Cerebral salt wasting syndrome (CSWS) is characterized by severe natriuresis and volume depletion in the presence of cerebral pathology. In literature, there are few reports about tuberculous meningitis and cerebral CSWS. In this article, we report two tuberculous meningitis cases with CSWS and present a review of the literature on this topic. Cerebral salt wasting diagnosis was based on hypona...
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ژورنال
عنوان ژورنال: Journal of Clinical Case Reports
سال: 2016
ISSN: 2165-7920
DOI: 10.4172/2165-7920.1000841