Primary parenchymal cerebral cystic haemangiopericytoma: A 5‐year follow up of disease progression

Summary Haemangiopericytoma (HPC) is a rare tumour of the cental nervous system. Previously, HPCs were thought to originate from meninges and ventricular walls. Currently, they are accepted as distinctive mesenchymal neoplasms unrelated to meningiomas. Imaging appearances, clinical progression and h...

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Published inAustralasian radiology Vol. 47; no. 1; pp. 88 - 91
Main Authors Kuzeyli, Kayhan, Çakir, Ertuğrul, Karaarslan, Gokalp, Usul, Haydar, Reis, Abdülkadir, Baykal, Süleyman, Dinç, Hasan, Sari, Ahmet
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Science Pty 01.03.2003
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Summary:Summary Haemangiopericytoma (HPC) is a rare tumour of the cental nervous system. Previously, HPCs were thought to originate from meninges and ventricular walls. Currently, they are accepted as distinctive mesenchymal neoplasms unrelated to meningiomas. Imaging appearances, clinical progression and haemorrhage into a cystic tumour is documented in  an 18‐year‐old man where the final diagnosis, with histopathological verification, proved to be a cystic HPC. This interesting and illustrative case is discussed with the relevant literature.
Bibliography:S Baykal
A Sari
E Çakir
H Usul
H Dinç
MD.
MD
G Karaarslan
A Reis
K Kuzeyli
ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
ISSN:0004-8461
1440-1673
DOI:10.1046/j.1440-1673.2003.01114.x