Diencephalic syndrome

1310 Diencephalon

Diencephalic syndrome is a rare clinical condition primarily affecting infants and young children. It is characterized by severe emaciation despite normal or slightly decreased caloric intake, and it is often associated with central nervous system tumors, particularly those located in the diencephalon region of the brain.

Presentation

The hallmark of diencephalic syndrome is profound failure to thrive despite adequate or even increased caloric intake. Other common symptoms include:

• Hyperactivity
• Irritability
• Vomiting
• Pallor
• Hypoglycemia
• Nystagmus
• Visual disturbances

Causes

Diencephalic syndrome is most commonly associated with low-grade gliomas in the diencephalon, particularly optic pathway gliomas. These tumors can disrupt the normal function of the hypothalamus, leading to the characteristic symptoms of the syndrome.

Diagnosis

Diagnosis of diencephalic syndrome typically involves a combination of clinical evaluation and imaging studies. Magnetic resonance imaging (MRI) is the preferred method for identifying tumors in the diencephalon. Additional tests may include:

• Endocrine evaluation to assess hypothalamic function
• Blood tests to check for metabolic abnormalities
• Ophthalmologic examination to evaluate visual disturbances

Treatment

The primary treatment for diencephalic syndrome is the management of the underlying tumor. Treatment options may include:

• Surgery to remove the tumor
• Radiation therapy
• Chemotherapy

Nutritional support is also crucial to address the severe emaciation and failure to thrive. This may involve:

• High-calorie diet
• Nutritional supplements
• Feeding tubes in severe cases

Prognosis

The prognosis for diencephalic syndrome varies depending on the nature and location of the tumor, as well as the response to treatment. Early diagnosis and intervention are critical for improving outcomes.

Related Pages

• Diencephalon
• Hypothalamus
• Optic pathway glioma
• Failure to thrive
• Central nervous system