Selected Publication:
Fink-Puches, R; Smolle, J; Beham, A; Kerl, H; Soyer, HP.
Cutaneous angiosarcoma].
Hautarzt. 2000; 51(7):479-485
Doi: 10.1007/s001050051157
Web of Science
PubMed
FullText
FullText_MUG
- Leading authors Med Uni Graz
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Fink-Puches Regina
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Soyer Hans Peter
- Co-authors Med Uni Graz
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Beham Alfred
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Kerl Helmut
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Smolle Josef
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- Abstract:
- Background and Objectives. Angiosarcomas of the skin arise almost exclusively in the following clinical settings: 1.the face and scalp, usually in elderly individuals, 2. lymphedematous regions (lymphedema-associated angiosarcomas), and 3.skin that has been previously irrradiated (post-radiation angiosarcomas). Clinical and histopathologic diagnosis of angiosarcoma is difficult often resulting in great delay that obviates against early and possibly successful treatment of these very aggressive neoplasms. Diagnostic problems are described, and prognostic factors as well as the effect of different forms of treatment on the outcome are discussed.Patients/Methods. Retrospective study of 11 patients with cutaneous angiosarcomas. Clinical presentation, histopathology, therapy and survival time are analysed.Results. Only 1 of 11 cases cutaneous angiosarcoma was clinically identified. Survival time was 1-24 months. Three patients who received radical surgery have not developed metastases and are still alive.Conclusions. Clinical and histopathologic diagnosis of cutaneous angiosarcomas is often Very difficult. Prognosis is very bad; radical surgery seems to be the best therapeutical option.
- Find related publications in this database (using NLM MeSH Indexing)
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Adult -
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Aged -
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Aged, 80 and over -
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Female -
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Hemangiosarcoma - diagnosis
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Humans -
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Male -
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Middle Aged -
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Neoplasms, Radiation-Induced - diagnosis
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Prognosis -
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Skin - pathology
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Skin Neoplasms - diagnosis
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Survival Rate -
- Find related publications in this database (Keywords)
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cutaneous angiosarcoma
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angiosarcoma of the face and scalp
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lymphedema-associated angiosarcoma
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radiation-induced angiosarcoma
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diagnostic difficulties