Endometrioid adenocarcinoma of the ovary mimicking serous borderline tumor: report of a series of cases
other
OA: closed
public-domain-us
⚙
AI-generated summary
by qwen3.7-flash, 2026-08-31
ⓘ
This report describes five cases of ovarian endometrioid adenocarcinoma mimicking serous borderline tumors, highlighting that extensive sampling and WT1 immunohistochemistry are valuable diagnostic tools to distinguish these malignancies.
⚙
AI-generated deep summary
by qwen3.7-flash, 2026-08-22
· read from full text
ⓘ
This study presents a series of five ovarian endometrioid adenocarcinomas that were initially misdiagnosed or suspected to be serous borderline tumors due to their predominant papillary architecture and bland epithelial cells. The authors identify specific diagnostic features that distinguish these malignancies, including monomorphous cell populations, cytoplasmic clearing, pronounced nuclear atypia, mitotic activity, squamous elements, and absent or focal WT1 staining. They emphasize that the presence of associated endometriosis is a useful clue in confirming an endometrioid neoplasm amidst this diagnostic pitfall. This paper is centrally about endometriosis, as it highlights endometriosis as a key histological feature aiding in the differential diagnosis of ovarian endometrioid adenocarcinoma.
Abstract
Ovarian endometrioid adenocarcinomas may have an extremely variable morphologic appearance and mimic a number of other epithelial malignancies as well as nonepithelial tumors. We report the clinicopathologic features of a small series of ovarian endometrioid adenocarcinomas (n=5), 4 of which were received in consultation, which were originally diagnosed as or were suspected to represent serous borderline tumor, with or without a component of low-grade serous adenocarcinoma. The patients were aged between 47 and 74 yr (mean, 60 yr), and all tumors were unilateral and Stage 1C. Serous borderline tumor was suspected on the basis of the predominant architectural pattern with prominent papillary formations consisting of rather bland epithelial cells covering stromal cores which projected into cystic spaces. In all cases, there were areas of typical endometrioid adenocarcinoma, although these foci were minor. Features useful in confirming an endometrioid neoplasm, not all of which were present in every case, were a monomorphous cell population, areas of cytoplasmic clearing, areas of more pronounced nuclear atypia, and mitotic activity than is typical of low-grade serous neoplasms, squamous elements, endometriosis and absent or only focal WT1 immunohistochemical staining. The close mimicry of a serous borderline tumor by an endometrioid adenocarcinoma is a diagnostic pitfall which has not been reported in the literature and represents yet another example of the propensity for ovarian endometrioid adenocarcinomas to mimic other neoplasms. Pathologists should consider an endometrioid adenocarcinoma when faced with a presumed serous borderline tumor with any of the features listed above. Extensive sampling may be of value in revealing more typical areas of endometrioid neoplasia and negative staining with WT1 of use in excluding a serous neoplasm.
Full text
2,012 characters
· extracted from
oa-doi-fallback
· click to expand
Endometrioid Adenocarcinoma of the Ovary Mimicking Serous Borderline Tumor
Report of a Series of Cases
- Sorsiah Mansor
- W. Glenn McCluggage
Ovarian endometrioid adenocarcinomas may have an extremely variable morphologic appearance and mimic a number of other epithelial malignancies as well as nonepithelial tumors. We report the clinicopathologic features of a small series of ovarian endometrioid adenocarcinomas (n=5), 4 of which were received in consultation, which were originally diagnosed as or were suspected to represent serous borderline tumor, with or without a component of low-grade serous adenocarcinoma. The patients were aged between 47 and 74 yr (mean, 60 yr), and all tumors were unilateral and Stage 1C. Serous borderline tumor was suspected on the basis of the predominant architectural pattern with prominent papillary formations consisting of rather bland epithelial cells covering stromal cores which projected into cystic spaces. In all cases, there were areas of typical endometrioid adenocarcinoma, although these foci were minor. Features useful in confirming an endometrioid neoplasm, not all of which were present in every case, were a monomorphous cell population, areas of cytoplasmic clearing, areas of more pronounced nuclear atypia, and mitotic activity than is typical of low-grade serous neoplasms, squamous elements, endometriosis and absent or only focal WT1 immunohistochemical staining. The close mimicry of a serous borderline tumor by an endometrioid adenocarcinoma is a diagnostic pitfall which has not been reported in the literature and represents yet another example of the propensity for ovarian endometrioid adenocarcinomas to mimic other neoplasms. Pathologists should consider an endometrioid adenocarcinoma when faced with a presumed serous borderline tumor with any of the features listed above. Extensive sampling may be of value in revealing more typical areas of endometrioid neoplasia and negative staining with WT1 of use in excluding a serous neoplasm.
Text is read by the "Ask this paper" AI Q&A widget below.
Extraction quality varies by source — PMC NXML preserves structure
cleanly, OA-HTML may include some navigation residue, and OA-PDF can
have broken hyphenation. The publisher copy
(via DOI)
is the canonical version.
My notes (saved in your browser only)
⚙
Ask this paper
AI returns verbatim quotes from the full text
· source: oa-doi-fallback
ⓘ
Condition tags
endometriosis
MeSH descriptors
Carcinoma, Endometrioid
Cystadenocarcinoma, Serous
Ovarian Neoplasms
Ovary
Aged
Biomarkers, Tumor
Biomarkers, Tumor
Carcinoma, Endometrioid
Carcinoma, Endometrioid
Carcinoma, Endometrioid
Cystadenocarcinoma, Serous
Cystadenocarcinoma, Serous
Cystadenocarcinoma, Serous
Diagnosis, Differential
Female
Humans
Immunohistochemistry
Middle Aged
Ovarian Neoplasms
Ovarian Neoplasms
Citation neighborhood
(no data yet)
We don't have any in-corpus citations linked to this paper yet.
The paper's references may be in our DB but unresolved to
``paper_id`` (resolution happens at ingest when the cited DOI
matches a row we already have). Run the cross-source citation
reconcile pass to retry.
Source provenance
- europepmc
- last seen: 2026-09-12T06:55:35.949492+00:00
- pubmed
- last seen: 2026-05-13T22:18:22.440000+00:00
- unpaywall
- last seen: 2026-09-11T06:32:28.951138+00:00
License: public-domain-us
· commercial use OK
· attribution required
Courtesy of the U.S. National Library of Medicine