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 in | Australasian radiology Vol. 47; no. 1; pp. 88 - 91 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Science Pty
01.03.2003
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Subjects | |
Online Access | Get full text |
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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. |
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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 |