Rare tumours of the heart - angiosarcomas

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11140%2F14%3A10271879" target="_blank" >RIV/00216208:11140/14:10271879 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00669806:_____/14:10271879

Výsledek na webu

<a href="http://www.termedia.pl/Case-report-Rare-tumors-of-the-heart-angiosarcomas-Two-case-reports,77,22246,1,1.html" target="_blank" >http://www.termedia.pl/Case-report-Rare-tumors-of-the-heart-angiosarcomas-Two-case-reports,77,22246,1,1.html</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.5114/wo.2014.40601" target="_blank" >10.5114/wo.2014.40601</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Rare tumours of the heart - angiosarcomas

Popis výsledku v původním jazyce

Primary tumours of the heart are very rare. Reported prevalence is about 0.001-0.3% of routine autopsies [1, 2]. More than three-quarters of them are benign, with myxoma as the most often histological type. The malignant primary tumours of the heart areangiosarcomas, rhabdomyosarcoma, osteosarcoma, leiomyosarcoma, undifferentiated sarcoma and primary cardiac lymphoma [3]. Angiosarcoma is, with its prevalence 0.000075-0.00225%, the most common of them [4, 5]. The very poor prognosis of this disease is caused by its late diagnosis and treatment because of limited information on the clinical aspects for this type of tumour. The mean overall survive is from 6 to 13 months [5, 6]. Two cases, treated in the Department of Oncology and Radiotherapy at the University Hospital in Pilsen, are presented in this paper.

Název v anglickém jazyce

Rare tumours of the heart - angiosarcomas

Popis výsledku anglicky

Primary tumours of the heart are very rare. Reported prevalence is about 0.001-0.3% of routine autopsies [1, 2]. More than three-quarters of them are benign, with myxoma as the most often histological type. The malignant primary tumours of the heart areangiosarcomas, rhabdomyosarcoma, osteosarcoma, leiomyosarcoma, undifferentiated sarcoma and primary cardiac lymphoma [3]. Angiosarcoma is, with its prevalence 0.000075-0.00225%, the most common of them [4, 5]. The very poor prognosis of this disease is caused by its late diagnosis and treatment because of limited information on the clinical aspects for this type of tumour. The mean overall survive is from 6 to 13 months [5, 6]. Two cases, treated in the Department of Oncology and Radiotherapy at the University Hospital in Pilsen, are presented in this paper.

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

FD - Onkologie a hematologie

OECD FORD obor

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Projekt

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Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2014

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Wspolczesna Onkologia

ISSN

1428-2526

e-ISSN

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Svazek periodika

18

Číslo periodika v rámci svazku

Special Issues

Stát vydavatele periodika

PL - Polská republika

Počet stran výsledku

4

Strana od-do

1-4

Kód UT WoS článku

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EID výsledku v databázi Scopus

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