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Endometrioid tumor

human disease

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Record originEnglish Wikipedia
Text licenseCC BY-SA 4.0
Source revisionJan 3, 2025
Entity authorityQ5376366
Source-derived summary

Endometrioid tumors are a class of tumors that arise in the uterus or ovaries that resemble endometrial glands on histology. They account for 80% of endometrial carcinomas and 20% of malignant ovarian tumors.

Ovary

Ovarian endometrioid tumors are part of the surface epithelial tumor group of ovarian neoplasms (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 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.

Endometrium

Endometrioid carcinoma can also arise in the endometrium.

Grades 1 and 2 are considered "type 1" endometrial cancer, while grade 3 is considered "type 2".

Light microscopy

Light microscopy shows tubular glands, resembling endometrium.

Editorial summary

This brief starts where responsible research should: with the source description of “Endometrioid tumor” as human disease. Everything that follows is an evidence route, not borrowed authority.

Editorial reviewA concise reference frame for defining the subject, testing terminology and identifying the institution closest to the evidence. The current 141-word lead offers orientation but no explicit four-digit date, so chronology should not be assumed. The selected authority fields contribute no independent date. The account is most persuasive where Endometrioid, tumor and human can be independently traced.
Editorial analysis

Why this record matters

The subject matters to the general reference register because the source frames it as human disease. Its deeper value depends on whether names, dates, institutions and citations support that framing.

Evidence profile

Named sources, stable identifiers and responsible institutions provide the strongest route from overview to verifiable evidence. The source revision retrieved here is dated Jan 3, 2025. The linked authority identifier is Q5376366. None of the 0 selected statements returned an explicit reference.

Critical limits

The absence of detail may reflect summary conventions rather than a lack of surviving documentation. The source lead contains qualifying language; that uncertainty should survive quotation, summary and reuse. Authority statements aid reconciliation but still require their own references, qualifiers and ranks to be checked.

How to read it

Use the entry as an orientation point, then follow its citations and revision history. Names, dates and institutional relationships should be checked against the original record.

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The closest primary source, responsible institution and strongest cited specialist reference.

Three-step research path

  1. Establish the record: confirm the title “Endometrioid tumor”, its source revision and the description used here.
  2. Expand the search: follow Endometrioid tumor primary sources, Endometrioid tumor archive and Endometrioid research across catalogues and specialist indexes.
  3. Test the account: compare the strongest cited source with the responsible institution’s current record and note any disagreement.

Questions for further research

  1. Which source most directly establishes the central claim about “Endometrioid tumor”?
  2. What terminology or title could unlock a more precise catalogue search?
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Source & attribution

This entry incorporates text from Endometrioid tumor” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.