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10.1186/s40661-015-0008-z

http://scihub22266oqcxt.onion/10.1186/s40661-015-0008-z
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C4880836!4880836!27231561
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suck abstract from ncbi


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pmid27231561      Gynecol+Oncol+Res+Pract 2015 ; 2 (ä): ä
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  • Adenocarcinoma of Mullerian origin: review of pathogenesis, molecular biology, and emerging treatment paradigms #MMPMID27231561
  • Cobb LP; Gaillard S; Wang Y; Shih Ie-M; Secord AA
  • Gynecol Oncol Res Pract 2015[]; 2 (ä): ä PMID27231561show ga
  • Traditionally, epithelial ovarian, tubal, and peritoneal cancers have been viewed as separate entities with disparate origins, pathogenesis, clinical features, and outcomes. Additionally, previous classification systems for ovarian cancer have proposed two primary histologic groups that encompass the standard histologic subtypes. Recent data suggest that these groupings no longer accurately reflect our knowledge surrounding these cancers. In this review, we propose that epithelial ovarian, tubal, and peritoneal carcinomas represent a spectrum of disease that originates in the Mullerian compartment. We will discuss the incidence, classification, origin, molecular determinants, and pathologic analysis of these cancers that support the conclusion they should be collectively referred to as adenocarcinomas of Mullerian origin. As our understanding of the molecular and pathologic profiling of adenocarcinomas of Mullerian origin advances, we anticipate treatment paradigms will shift towards genomic driven therapeutic interventions.
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