The histogenesis of dural-based or ''central'' hemangiopericytomas (cH
PCs) remains controversial. Some authors consider these tumors variant
s of meningiomas while others consider them akin to peripheral hemangi
opericytomas (pHPCs). Meningiomas frequently have mutations in the neu
rofibromatosis 2 (NF2) gene, providing a molecular marker for meningio
mas and other NF2-related tumors. We therefore analyzed the NF2-relate
d tumors. We therefor analyzed the NF2 gene in cHPCs, pHPCs, and menin
giomas to determine whether cHPCs are more similar at the molecular ge
netic level to meningiomas or hPHCs. Using paraffin-embedded archival
material from 28 cHPCs (including three primary and recurrent tumors),
10 pHPCs, and 26 meningiomas, we scanned all 17 exons of the NF2 gene
and flanking intronic sequences for mutations with single strand conf
ormation polymorphism analysis and DNA sequencing. No NF2 mutations we
re found in either cHPCs or pHPCs, whereas 355 of meningiomas had NF2
gene alterations (P < 0.001). The NF2 gene mutations in meningiomas we
re all truncating mutations, consistent with previous studies. Our fin
dings suggest that cHPCs are distinct from meningiomas at the molecula
r genetic level and support prior clinico-pathological data that disti
nguish these tumor-entities.