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Cerebral salt wasting syndrome in a child with central diabetes insipidus following surgery for recurrent craniopharyngioma: A case report. | LitMetric

Cerebral salt wasting syndrome in a child with central diabetes insipidus following surgery for recurrent craniopharyngioma: A case report.

SAGE Open Med Case Rep

Unidad de Revisiones Sistemáticas y Meta-análisis, Vicerrectorado de Investigación, Universidad San Ignacio de Loyola, Lima, Peru.

Published: October 2024

AI Article Synopsis

  • - Surgical treatment of craniopharyngiomas in kids can lead to serious conditions like central diabetes insipidus (CDI) and cerebral salt wasting syndrome (CSWS), which together are rare and can be deadly.
  • - The article discusses a specific case of a 6-year-old boy who developed CDI and CSWS after surgery for a recurring tumor, highlighting the challenges of managing these conditions.
  • - Fludrocortisone was effective in treating the child’s CSWS, and this case could contribute to future research on managing similar pediatric conditions.

Article Abstract

Surgical treatment of craniopharyngiomas in children can produce disorders related to water and sodium such as central diabetes insipidus (CDI) and cerebral salt wasting syndrome (CSWS). The combination of both in children is unusually reported in the literature and is associated with high mortality. The management of CSWS is based on fluid therapy. Fludrocortisone is useful in children with CSWS who do not respond to fluid management. The objective of the paper is to describe the case of 6 years and 10 months old male child with hypopituitarism secondary to a craniopharyngioma surgery performed 7 months before, who presented to the emergency department due to recurrent craniopharyngioma. The child presented a combination of CDI and CSWS following surgery for this recurrent tumor. Therapy with fludrocortisone was effective. Pediatric patients as the one of this report can help build the foundation for subsequent systematic reviews or trials.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11462566PMC
http://dx.doi.org/10.1177/2050313X241275445DOI Listing

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