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Cerebral salt wasting in a child with cervicothoracic hematoma
Enver Simsek1, Dilek Dilli, Ugur Yasitli
1Department of Paediatric Endocrinology, Ministry of Health Ankara Training and Research Hospital, Ankara, Turkey.
Insights
Cerebral salt wasting (CSW) is a rare cause of hyponatremia in children, distinct from SIADH. Prompt diagnosis and fluid expansion are crucial for managing CSW in pediatric trauma patients.
Area of Science:
- Pediatric Neurology
- Nephrology
- Trauma Medicine
Background:
- Syndrome of inappropriate antidiuretic hormone secretion (SIADH) and cerebral salt wasting (CSW) are common causes of hyponatremia in CNS disorders.
- CSW is rarely reported in children, presenting diagnostic and therapeutic challenges.
- Distinguishing between SIADH and CSW is critical due to differing management strategies.
Observation:
- A pediatric case of cervicothoracic hematoma secondary to trauma presented with hyponatremia.
- Cerebral salt wasting (CSW) was diagnosed based on high urinary sodium excretion, hyponatremia, and low serum osmolarity.
- Absence of brain edema did not rule out CSW.
Findings:
- The patient exhibited high urinary sodium excretion and hyponatremia, consistent with CSW.
- Serum sodium levels improved with saline hydration, confirming the CSW diagnosis.
- This case highlights CSW as a potential cause of hyponatremia in pediatric trauma.
Implications:
- Cerebral salt wasting (CSW) should be considered in pediatric patients with cervicothoracic hematoma and hyponatremia, even without brain edema.
- Accurate diagnosis of CSW is essential for appropriate management, contrasting with SIADH treatment.
- Early identification and fluid expansion therapy can prevent complications in pediatric CSW cases.
Abstract:
Although the syndrome of inappropriate antidiuretic hormone secretion (SIADH) is commonly observed in patients with acute or chronic central nervous system (CNS) disorders, cerebral salt wasting (CSW) that results in hyponatremia has rarely been reported in children. Both SIADH and CSW result in increased urinary sodium excretion and hyponatremia. However, the management protocols for these two conditions are quite different; volume restriction is used in treating SIADH, while volume expansion is necessary for the treatment of CSW. We present a case of CSW in a child with cervicothoracic hematoma secondary to head and cervicothoracic trauma, without evidence of brain edema. The child was diagnosed on the basis of high urinary sodium excretion resulting in hyponatremia and low serum osmolarity. Improvements in serum sodium levels after saline hydration confirmed this diagnosis. We believe that potentially dangerous cases of hyponatremia should be carefully evaluated in children with cervicothoracic hematoma secondary to trauma, including situations in which brain edema is absent.
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