Diencephalic syndrome

The diencephalon, which is affected by diencaphalic syndrome, consists of the thalamus, the subthalamus, the hypothalamus, and the epithalamus.

Diencephalic syndrome, diencephalic syndrome of emaciation or Russell's syndrome is a rare neurological disorder seen in infants and children and characterised by failure to thrive and severe emaciation despite normal or slightly decreased caloric intake, locomotor hyperactivity, and euphoria. Less commonly it may involve skin pallor without anaemia, hypoglycaemia, and hypotension.[1] The syndrome is a rare but potentially fatal cause of failure to thrive in children. Failure to thrive presents on average at 7 months of age.[1] Of note the syndrome is not associated with developmental delay.[2] There may be associated hydrocephalus.

Diencephalic syndrome was first described by Russell in 1951.[3] It is usually caused by a brain tumor such as a low-grade glioma or astrocytoma located in the hypothalamic-optic chiasmatic region.[1] It is not yet understood how diencephalic syndrome causes the effects on appetite and metabolism which are seen, though inappropriately high growth hormone release has been proposed,[4] as has excessive β-lipotropin secretion[1] and overall increased metabolic demand.[5] It is treated with nutritional optimisation while the underlying lesion is treated with chemotherapy, surgery or radiotherapy.

References

  1. 1 2 3 4 Kim A, Moon JS, Yang HR, Chang JY, Ko JS, Seo JK (Jan 2015). "Diencephalic syndrome: a frequently neglected cause of failure to thrive in infants". Korean J Pediatr. 58 (1): 28–32. doi:10.3345/kjp.2015.58.1.28. PMID 25729396.
  2. Fleischman A1, Brue C, Poussaint TY, Kieran M, Pomeroy SL, Goumnerova L, Scott RM, Cohen LE (June 2005). "Diencephalic syndrome: a cause of failure to thrive and a model of partial growth hormone resistance". Pediatrics. 115 (6): 724–6. doi:10.1542/peds.2004-2237. PMID 15930202.
  3. Russell A (1951). "A diencephalic syndrome of emaciation in infancy and childhood". Arch Dis Child. 26: 274.
  4. Drop SL, Guyda HJ, Colle E (August 1980). "Inappropriate growth hormone release in the diencephalic syndrome of childhood: case report and 4 year endocrinological follow-up". Clin Endocrinol (Oxf). 13 (2): 181–7. doi:10.1111/j.1365-2265.1980.tb01040.x. PMID 7438472.
  5. Vlachopapadopoulou E, Tracey KJ, Capella M, Gilker C, Matthews DE (June 1993). "Increased energy expenditure in a patient with diencephalic syndrome". J Pediatr. 112 (6): 922–4. doi:10.1016/s0022-3476(09)90021-x. PMID 8501572.
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