Ra. Kristof et al., INTRAVASCULAR PAPILLARY ENDOTHELIAL HYPERPLASIA OF THE SELLAR REGION - REPORT OF 3 CASES AND REVIEW OF THE LITERATURE, Journal of neurosurgery, 86(3), 1997, pp. 558-563
Intravascular papillary endothelial hyperplasia (IPEH) is considered a
reactive proliferation of endothelium associated with thrombosis. The
occurrence of IPEH in the cranial cavity is exceedingly rare. In this
article, the authors report three cases of IPEH that originated from
the cavernous sinus and extended into the sellar contents. The lesions
were resected incompletely in two cases and completely in one case. T
he IPEH in one of the patients was incompletely resected and exhibited
further growth on magnetic resonance imaging 3 months postoperatively
; local radiation therapy was instituted. This led to shrinkage of the
lesion over an additional follow-up period of 3.5 years. In a review
of the literature, the authors located seven other cases of intracrani
al IPEH. The authors conclude that clinically symptomatic intracranial
IPEH should be completely resected whenever possible, because it can
cause considerable morbidity and mortality and because it is prone to
progression or recurrence.