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Dedifferentiated endometrioid adenocarcinoma; clinicopathologic and immunohistochemical features of five cases
OBJECTIVE: Dedifferentiated endometrioid adenocarcinoma is a recently defined uterine tumor composed of low-grade endometrioid adenocarcinoma and undifferentiated carcinoma. Herein, we present clinicopathologic, morphologic, and immunohistochemical features of 5 cases of dedifferentiated endometrioi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Galenos Publishing
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085529/ https://www.ncbi.nlm.nih.gov/pubmed/29545232 http://dx.doi.org/10.4274/jtgga.2017.0090 |
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author | Yiğit, Seyran Ekinci, Neşe Hayrullah, Leyla Öcal, İrfan Bezircioğlu, İncim |
author_facet | Yiğit, Seyran Ekinci, Neşe Hayrullah, Leyla Öcal, İrfan Bezircioğlu, İncim |
author_sort | Yiğit, Seyran |
collection | PubMed |
description | OBJECTIVE: Dedifferentiated endometrioid adenocarcinoma is a recently defined uterine tumor composed of low-grade endometrioid adenocarcinoma and undifferentiated carcinoma. Herein, we present clinicopathologic, morphologic, and immunohistochemical features of 5 cases of dedifferentiated endometrioid adenocarcinoma. MATERIAL AND METHODS: All cases which were diagnosed as mixed endometrial adenocarcinoma (endometrioid+undifferentiated carcinoma) or dedifferentiated endometrioid adenocarcinoma between January 2008 and December 2014 were retrieved from the archives of our institution’s pathology department. RESULTS: The median age of the patients was 58 years. Polypoid growth pattern was seen in 3 patients and 2 were diagnosed at advanced stage. All patients received either external radiotherapy, brachytherapy, chemotherapy or an appropriate combination according to the stage. Only one patient died of the disease. Microscopically, there was a sharp demarcation between the two tumor components. The undifferentiated carcinoma component was composed of diffuse sheets of monomorphic cells lacking any differentiation. Focal pleomorphism and rhabdoid features were also noted. The undifferentiated carcinoma component was variably positive for PAX-8, cytokeratin, EMA, estrogen receptor, and neuroendocrine markers. CONCLUSION: Misdiagnosis of undifferentiated carcinoma in dedifferentiated endometrioid adenocarcinoma as grade 3 endometrioid adenocarcinoma is not uncommon. The recognition of morphologic and immunohistochemical features of this newly described entity is crucial because it alters treatment and prognosis. |
format | Online Article Text |
id | pubmed-6085529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Galenos Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-60855292018-08-14 Dedifferentiated endometrioid adenocarcinoma; clinicopathologic and immunohistochemical features of five cases Yiğit, Seyran Ekinci, Neşe Hayrullah, Leyla Öcal, İrfan Bezircioğlu, İncim J Turk Ger Gynecol Assoc Original Investigation OBJECTIVE: Dedifferentiated endometrioid adenocarcinoma is a recently defined uterine tumor composed of low-grade endometrioid adenocarcinoma and undifferentiated carcinoma. Herein, we present clinicopathologic, morphologic, and immunohistochemical features of 5 cases of dedifferentiated endometrioid adenocarcinoma. MATERIAL AND METHODS: All cases which were diagnosed as mixed endometrial adenocarcinoma (endometrioid+undifferentiated carcinoma) or dedifferentiated endometrioid adenocarcinoma between January 2008 and December 2014 were retrieved from the archives of our institution’s pathology department. RESULTS: The median age of the patients was 58 years. Polypoid growth pattern was seen in 3 patients and 2 were diagnosed at advanced stage. All patients received either external radiotherapy, brachytherapy, chemotherapy or an appropriate combination according to the stage. Only one patient died of the disease. Microscopically, there was a sharp demarcation between the two tumor components. The undifferentiated carcinoma component was composed of diffuse sheets of monomorphic cells lacking any differentiation. Focal pleomorphism and rhabdoid features were also noted. The undifferentiated carcinoma component was variably positive for PAX-8, cytokeratin, EMA, estrogen receptor, and neuroendocrine markers. CONCLUSION: Misdiagnosis of undifferentiated carcinoma in dedifferentiated endometrioid adenocarcinoma as grade 3 endometrioid adenocarcinoma is not uncommon. The recognition of morphologic and immunohistochemical features of this newly described entity is crucial because it alters treatment and prognosis. Galenos Publishing 2018-09 2018-08-06 /pmc/articles/PMC6085529/ /pubmed/29545232 http://dx.doi.org/10.4274/jtgga.2017.0090 Text en ©Copyright 2018 by the Turkish-German Gynecological Education and Research Foundation http://creativecommons.org/licenses/by/2.5/ Journal of the Turkish-German Gynecological Association |
spellingShingle | Original Investigation Yiğit, Seyran Ekinci, Neşe Hayrullah, Leyla Öcal, İrfan Bezircioğlu, İncim Dedifferentiated endometrioid adenocarcinoma; clinicopathologic and immunohistochemical features of five cases |
title | Dedifferentiated endometrioid adenocarcinoma; clinicopathologic and immunohistochemical features of five cases |
title_full | Dedifferentiated endometrioid adenocarcinoma; clinicopathologic and immunohistochemical features of five cases |
title_fullStr | Dedifferentiated endometrioid adenocarcinoma; clinicopathologic and immunohistochemical features of five cases |
title_full_unstemmed | Dedifferentiated endometrioid adenocarcinoma; clinicopathologic and immunohistochemical features of five cases |
title_short | Dedifferentiated endometrioid adenocarcinoma; clinicopathologic and immunohistochemical features of five cases |
title_sort | dedifferentiated endometrioid adenocarcinoma; clinicopathologic and immunohistochemical features of five cases |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085529/ https://www.ncbi.nlm.nih.gov/pubmed/29545232 http://dx.doi.org/10.4274/jtgga.2017.0090 |
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