Cerebral neoplasms are uncommon in pregnancy but should be considered in any pregnant woman with new onset neurological symptoms and signs. We report a case of cerebellar haemangioblastoma presenting in pregnancy and discuss the clinical presentation, diagnosis, surgical management and medical literature surrounding the condition.
HaasJF, JanischW, StaneczekW. Newly diagnosed primary intracranial neoplasms in pregnant women: a population based assessment. J Neurol Neurosurg Psychiatry1986;49:7
3.
OthmaneIS, ShieldsC, SinghA, ShieldsJ, GoldmanW. Postpartum cerebellar herniation in von Hippel–Lindau syndrome. Am J Ophthalmol1999;128:387–9
DemiraranY, OzgonM, UtkuT, BozkurtP. Epidural anaesthesia for caesarean section in a patient with von Hippel–Lindau disease. Eur J Anaesthesiol2001;18:330–2
6.
BokerA, OngBY. Anesthesia for cesarean section and posterior fossa craniotomy in a patient with von Hippel–Lindau disease. Can J Anaesthesia J Can D Anesthesie2001;48:387–90
7.
MaddockIR, MoranA, MaherER, A genetic register for von Hippel–Lindau disease. J Med Genet1996;33:120–7
8.
HesFJ, van der LuijtRB, JanssenALW, Frequency of von Hippel–Lindau germline mutations in classic and non-classic von Hippel–Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification. Clin Genet2007;72:122–9
9.
ZilidisG, Cadoux-HudsonTAD. Recurrent dural based cystic cerebellar haemangioblastoma in a patient with von Hippel–Lindau disease. Acta Neurochirurg2007;149:433–6
10.
VaqueroJS, MartinezR. Progesterone receptor proteins in cerebellar haemangioblastoma. Surg Neurol1984;21:2
11.
GrimbertP, ChauveauD, RichardS, RemyP, GrunfeldJP. Pregnancy in von Hippel–Lindau disease. Am J Obstet Gynecol1999;180:110–1
