2009
DOI: 10.1016/j.ygyno.2009.07.030
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An updated clinicopathologic study of early-stage uterine papillary serous carcinoma (UPSC)

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Cited by 119 publications
(73 citation statements)
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“…In support of extensive prior clinical and incidence surveys, we also found that Type II tumors are diagnosed more often among older and non-white women [8,[15][16][17][18][19][20]. These differences in risk factor relationships, in combination with the more frequent occurrence of Type II cancers after menopause, provide some of the strongest epidemiologic support that endometrial cancers are etiologically heterogeneous.…”
Section: Discussionsupporting
confidence: 77%
“…In support of extensive prior clinical and incidence surveys, we also found that Type II tumors are diagnosed more often among older and non-white women [8,[15][16][17][18][19][20]. These differences in risk factor relationships, in combination with the more frequent occurrence of Type II cancers after menopause, provide some of the strongest epidemiologic support that endometrial cancers are etiologically heterogeneous.…”
Section: Discussionsupporting
confidence: 77%
“…Unlike endometrioid carcinomas, aggressive endometrial carcinoma types, particularly serous carcinomas (14), may metastasize despite limited tumor volume in the uterus. Notably, "minimal uterine serous carcinoma" (15), which comprises approximately 20% of serous tumors (14,16), has been found to present with extra-uterine disease in up to 45% of women (17).…”
Section: Discussionmentioning
confidence: 99%
“…Notably, "minimal uterine serous carcinoma" (15), which comprises approximately 20% of serous tumors (14,16), has been found to present with extra-uterine disease in up to 45% of women (17). Further, molecular analysis in these cases suggests that intraand extra-uterine tumor cells are often clonally related (18)(19)(20)(21).…”
Section: Discussionmentioning
confidence: 99%
“…Slomovitz et al and Fader et al demonstrated that mixed histology and any percentage of USC in a mixedhistology specimen confer a risk for recurrence similar to that in a pure serous tumour. 6,26 We found no difference in prognosis between pure or mixed-histology USCs.…”
Section: Discussionmentioning
confidence: 56%