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    Vaginal haemangioendothelioma: an unusual tumour.

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    Authors
    Mohan, H
    Shireen, R
    Hayes, B
    Canney, A
    Mooney, E E
    Murphy, J
    Affiliation
    Department of Gynaecology, St Vincent's University Hospital, Elm Park, Dublin 4, , Ireland. eibhlinmohan@hotmail.com
    Issue Date
    2012-02-01T10:31:14Z
    MeSH
    Adult
    Female
    Hemangioendothelioma/*diagnosis/surgery
    Hemangiopericytoma/*diagnosis/surgery
    Humans
    Vaginal Neoplasms/*diagnosis/surgery
    
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    Citation
    Ir J Med Sci. 2009 Jun;178(2):223-5. Epub 2008 Feb 21.
    Journal
    Irish journal of medical science
    URI
    http://hdl.handle.net/10147/207556
    DOI
    10.1007/s11845-008-0138-y
    PubMed ID
    18288571
    Abstract
    Vaginal tumours are uncommon and this is a particularly rare case of a vaginal haemangioendothelioma in a 38-year-old woman. Initial presentation consisted of symptoms similar to uterovaginal prolapse with "something coming down". Examination under anaesthesia demonstrated a necrotic anterior vaginal wall tumour. Histology of the lesion revealed a haemangioendothelioma which had some features of haemangiopericytoma. While the natural history of vaginal haemangioendothelioma is uncertain, as a group, they have a propensity for local recurrence. To our knowledge this is the third reported case of a vaginal haemangioendothelioma. Management of this tumour is challenging given the paucity of literature on this tumour. There is a need to add rare tumours to our "knowledge bank" to guide management of these unusual tumours.
    Language
    eng
    ISSN
    1863-4362 (Electronic)
    0021-1265 (Linking)
    ae974a485f413a2113503eed53cd6c53
    10.1007/s11845-008-0138-y
    Scopus Count
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