Review of tubulocystic carcinoma of the kidney with focus on clinical and pathobiological aspects
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11140%2F13%3A10173933" target="_blank" >RIV/00216208:11140/13:10173933 - isvavai.cz</a>
Výsledek na webu
<a href="http://www.termedia.pl/Review-of-tubulocystic-carcinoma-of-the-kidney-with-focus-on-clinical-and-pathobiological-aspects,55,21888,1,1.html" target="_blank" >http://www.termedia.pl/Review-of-tubulocystic-carcinoma-of-the-kidney-with-focus-on-clinical-and-pathobiological-aspects,55,21888,1,1.html</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.5114/pjp.2013.39329" target="_blank" >10.5114/pjp.2013.39329</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Review of tubulocystic carcinoma of the kidney with focus on clinical and pathobiological aspects
Popis výsledku v původním jazyce
Tubulocystic carcinoma of the kidney (TCK) is a recently established entity in renal neoplastic pathology. This review aims to give an overview of the clinical and pathobiological aspects of TCK. Grossly, the TCKs are well-demarcated multicystic lesionsgiving a "wrapped bubble" or "spongy" appearance. Microscopically, the tumors are composed of multiple, variably sized cysts separated by thin fibrous septa lacking ovarian stroma or desmoplastic reaction. The cysts are lined by tumor cells with eosinophilic cytoplasm and nuclear atypia of variable, but not infrequently of high grade corresponding to Fuhrman grade 3. A frequent association with papillary tumors has been reported. Recent molecular genetic studies of TCK have revealed distinct features separating this subset of renal cell carcinomas (RCCs) from other types of renal tumors including collecting duct carcinoma of Bellini and renal medullary carcinoma as well as pointing towards a close kinship with papillary RCC. Tubulocysti
Název v anglickém jazyce
Review of tubulocystic carcinoma of the kidney with focus on clinical and pathobiological aspects
Popis výsledku anglicky
Tubulocystic carcinoma of the kidney (TCK) is a recently established entity in renal neoplastic pathology. This review aims to give an overview of the clinical and pathobiological aspects of TCK. Grossly, the TCKs are well-demarcated multicystic lesionsgiving a "wrapped bubble" or "spongy" appearance. Microscopically, the tumors are composed of multiple, variably sized cysts separated by thin fibrous septa lacking ovarian stroma or desmoplastic reaction. The cysts are lined by tumor cells with eosinophilic cytoplasm and nuclear atypia of variable, but not infrequently of high grade corresponding to Fuhrman grade 3. A frequent association with papillary tumors has been reported. Recent molecular genetic studies of TCK have revealed distinct features separating this subset of renal cell carcinomas (RCCs) from other types of renal tumors including collecting duct carcinoma of Bellini and renal medullary carcinoma as well as pointing towards a close kinship with papillary RCC. Tubulocysti
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
FP - Ostatní lékařské obory
OECD FORD obor
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Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2013
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Polish Journal of Pathology
ISSN
1233-9687
e-ISSN
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Svazek periodika
64
Číslo periodika v rámci svazku
4
Stát vydavatele periodika
PL - Polská republika
Počet stran výsledku
5
Strana od-do
233-237
Kód UT WoS článku
000330418200001
EID výsledku v databázi Scopus
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