The association of enchondromatosis with malignant transformed chondrosarcoma and ovarian juvenile granulosa cell tumor (Ollier disease)
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F17%3A10366589" target="_blank" >RIV/00216208:11110/17:10366589 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216208:11130/17:10366589 RIV/00064203:_____/17:10366589 RIV/00064211:_____/17:W0000025 RIV/00064165:_____/17:10366589
Výsledek na webu
<a href="http://dx.doi.org/10.1016/j.tjog.2017.02.002" target="_blank" >http://dx.doi.org/10.1016/j.tjog.2017.02.002</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.tjog.2017.02.002" target="_blank" >10.1016/j.tjog.2017.02.002</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
The association of enchondromatosis with malignant transformed chondrosarcoma and ovarian juvenile granulosa cell tumor (Ollier disease)
Popis výsledku v původním jazyce
Objective: Ovarian juvenile granulosa cell tumor has an interesting association with multiple enchondromatosis (Oilier disease and Maffucci syndrome) and should be considered a leading diagnosis when an ovarian mass is found in young patients with these conditions. Besides the association with nonskeletal malignancies, there is a high risk of malignant transformation of enchondroma in chondrosarcoma as was also the case in this instance. Case Report: The report uses multiple images to document the representative and characteristic markers of multiple enchondromas in a 22-year-old patient with Oilier disease complicated by malignant transformation of chondrosarcoma and in whom the disease is associated with ovarian juvenile granulosa cell tumor of the right ovary. Conclusion: It is important to recognize that when the female patient presents with enchondromatosis and a large unilateral multilocular-solid ovarian mass, the specific diagnosis of granulosa cell tumor can be made with high accuracy.
Název v anglickém jazyce
The association of enchondromatosis with malignant transformed chondrosarcoma and ovarian juvenile granulosa cell tumor (Ollier disease)
Popis výsledku anglicky
Objective: Ovarian juvenile granulosa cell tumor has an interesting association with multiple enchondromatosis (Oilier disease and Maffucci syndrome) and should be considered a leading diagnosis when an ovarian mass is found in young patients with these conditions. Besides the association with nonskeletal malignancies, there is a high risk of malignant transformation of enchondroma in chondrosarcoma as was also the case in this instance. Case Report: The report uses multiple images to document the representative and characteristic markers of multiple enchondromas in a 22-year-old patient with Oilier disease complicated by malignant transformation of chondrosarcoma and in whom the disease is associated with ovarian juvenile granulosa cell tumor of the right ovary. Conclusion: It is important to recognize that when the female patient presents with enchondromatosis and a large unilateral multilocular-solid ovarian mass, the specific diagnosis of granulosa cell tumor can be made with high accuracy.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30214 - Obstetrics and gynaecology
Návaznosti výsledku
Projekt
<a href="/cs/project/NT13070" target="_blank" >NT13070: Implementace ultrazvukového vyšetření do klinického stagingu karcinomu děložního hrdla</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2017
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Taiwanese Journal of Obstetrics and Gynecology
ISSN
1028-4559
e-ISSN
—
Svazek periodika
56
Číslo periodika v rámci svazku
2
Stát vydavatele periodika
TW - Čínská republika (Tchaj-wan)
Počet stran výsledku
5
Strana od-do
253-257
Kód UT WoS článku
000418316000027
EID výsledku v databázi Scopus
2-s2.0-85016212980