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No. 07-6215|place=Bethesda, MD|year=2007|chapter-url=http://seer.cancer.gov/publications/survival/surv_ovary.pdf|url=http://seer.cancer.gov/publications/survival/}}&lt;/ref> ''Endometrioid tumor'' is labeled at bottom left.]] Ovarian endometrioid tumors are part of the [[surface epithelial-stromal tumor|surface epithelial]] [[tumor]] group of [[Ovarian cancer|ovarian neoplasm]]s (10–20% of which are the endometrioid type). [[Benign]] and borderline variants are rare, as the majority are [[malignant]]. There is an association with [[endometriosis]] and concurrent primary [[endometrial carcinoma]] ([[endometrial cancer]]). On gross [[pathology|pathological]] examination, the tumor is cystic and may be solid and some arise in cystic endometriosis. In 40% of cases, endometrioid tumors are found bilaterally.&lt;ref>{{cite book |editor1-last=Robbins |editor2-last=Cotran |title=Pathologic Basis of Disease |location=Philadelphia |publisher=Saunders |edition=7th |isbn=978-0-7216-0187-8 |year=2005 }}&lt;/ref> ==Endometrium== Endometrioid carcinoma can also arise in the endometrium.&lt;ref name="pmid18156975">{{cite journal |vauthors=Mulvany NJ, Allen DG |title=Combined large cell neuroendocrine and endometrioid carcinoma of the endometrium |journal=Int. J. Gynecol. Pathol. |volume=27 |issue=1 |pages=49–57 |date=January 2008 |pmid=18156975 |doi=10.1097/pgp.0b013e31806219c5 |s2cid=43849133 }}&lt;/ref>&lt;ref>{{MeshName|Carcinoma,+Endometrioid}}&lt;/ref> Grades 1 and 2 are considered "type 1" [[endometrial cancer]], while grade 3 is considered "type 2".&lt;ref name="urlACS :: What Is Endometrial Cancer?">{{cite web |url=http://www.cancer.org/docroot/cri/content/cri_2_4_1x_what_is_endometrial_cancer.asp |title=ACS :: What Is Endometrial Cancer? |access-date=2010-03-24 |archive-date=2010-06-20 |archive-url=https://web.archive.org/web/20100620010337/http://www.cancer.org/docroot/cri/content/cri_2_4_1x_what_is_endometrial_cancer.asp |url-status=dead }}&lt;/ref> &lt;gallery mode="packed"> File:Pie chart of relative incidences of endometrial carcinoma.png|Relative incidences of [[endometrial carcinoma]]s by histopathology, being endometrioid in a majority of cases&lt;ref>{{cite journal|last1=Mendivil|first1=Alberto|last2=Schuler|first2=Kevin M.|last3=Gehrig|first3=Paola A.|title=Non-Endometrioid Adenocarcinoma of the Uterine Corpus: A Review of Selected Histological Subtypes|journal=Cancer Control|volume=16|issue=1|year=2009|pages=46–52|issn=1073-2748|doi=10.1177/107327480901600107|pmid=19078929}}&lt;/ref> &lt;/gallery> ==Light microscopy== [[Light microscopy]] shows tubular glands, resembling endometrium.&lt;ref>{{cite web|url=https://www.pathologyoutlines.com/topic/ovarytumorendometrioid.html|title=Ovary tumor - Endometrioid tumors - General|author=Shahrzad Ehdaivand|website=Pathology Outlines|access-date=2020-03-17|archive-date=2020-02-16|archive-url=https://web.archive.org/web/20200216103323/http://www.pathologyoutlines.com/topic/ovarytumorendometrioid.html|url-status=dead}} Topic Completed: 1 December 2012. Revised: 6 March 2020&lt;/ref> ==Molecular biology== ===CTNNB1 and PTEN mutations=== Ovarian and endometrial endometrioid carcinomas have distinct [[CTNNB1]] and PTEN [[mutation|gene mutation]] profiles. [[PTEN (gene)|PTEN]] mutations are more frequent in low-grade endometrial endometrioid carcinomas (67%) compared with low-grade ovarian endometrioid carcinomas (17%). By contrast, CTNNB1 mutations are significantly different in low-grade ovarian endometrioid carcinomas (53%) compared with low-grade endometrial endometrioid carcinomas (28%). This difference in CTNNB1 mutation frequency may be reflective of the distinct [[tumoral microenvironment]]s; the epithelial cells lining an [[endometriotic cyst]] within the [[ovary]] are exposed to a highly [[oxidative stress|oxidative environment]] that promotes [[tumorigenesis]].&lt;ref>{{Cite journal | pmid = 23765252| year = 2014| last1 = McConechy| first1 = M. K.| title = Ovarian and endometrial endometrioid carcinomas have distinct CTNNB1 and PTEN mutation profiles| journal = Modern Pathology| volume = 27| issue = 1| pages = 128–34| last2 = Ding| first2 = J| last3 = Senz| first3 = J| last4 = Yang| first4 = W| last5 = Melnyk| first5 = N| last6 = Tone| first6 = A. A.| last7 = Prentice| first7 = L. M.| last8 = Wiegand| first8 = K. C.| last9 = McAlpine| first9 = J. N.| last10 = Shah| first10 = S. P.| last11 = Lee| first11 = C. H.| last12 = Goodfellow| first12 = P. J.| last13 = Gilks| first13 = C. B.| last14 = Huntsman| first14 = D. G.| doi = 10.1038/modpathol.2013.107| pmc = 3915240}}&lt;/ref> ==References== {{reflist}} == External links == {{Medical resources | DiseasesDB = | ICD10 = | ICD9 = | ICDO = 8380-8381 | OMIM = | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = D018269 }} {{Tumor histology}} {{Breast cancer/urogenital neoplasia}} {{DEFAULTSORT:Endometrioid Tumor}} [[Category:Gynaecological cancer]] </textarea><div class="templatesUsed"><div class="mw-templatesUsedExplanation"><p><span id="templatesused">Pages transcluded onto the current version of this page<span class="posteditwindowhelplinks"> (<a href="/wiki/Help:Transclusion" title="Help:Transclusion">help</a>)</span>:</span> </p></div><ul> <li><a href="/wiki/Template:Breast_cancer/urogenital_neoplasia" class="mw-redirect" title="Template:Breast cancer/urogenital neoplasia">Template:Breast cancer/urogenital neoplasia</a> (<a href="/w/index.php?title=Template:Breast_cancer/urogenital_neoplasia&amp;action=edit" class="mw-redirect" 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