P. Wingenfeld et al., ACUTE GLAUCOMA AND INTRACRANIAL HYPERTENSION IN A CHILD ON LONG-TERM PERITONEAL-DIALYSIS TREATED WITH GROWTH-HORMONE, Pediatric nephrology, 9(6), 1995, pp. 742-745
A 7-year-old boy with end-stage renal disease on long-term peritoneal
dialysis is described. The child developed intracranial hypertension a
nd acute glaucoma during therapy with recombinant human growth hormone
(rhGH), 18 months after the onset of treatment, Symptoms developed wi
thin 1.5 days and required neurosurgical treatment to reduce the intra
cranial hypertension because of imminent impaction of the cerebellum a
nd brain stem. After ventricular cerebrospinal fluid drainage and cess
ation of growth hormone, all symptoms of intracranial hypertension and
increased intraocular pressure disappeared. To our knowledge this is
the first report of intracranial hypertension or hydrocephalus and acu
te glaucoma during rhGH therapy. Continuous and long-term control of t
he ophthalmological and neurological status of patients treated with r
hGh is indicated.