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IL-23 Expression in Stewart-Treves Syndrome: Two Case Reports and Immunohistochemical Investigation

Stewart-Treves syndrome (STS) is a rare cutaneous lymphangiosarcoma developing from chronic lymph edema as a consequence of radical mastectomy or surgical invasion of the groin for the treatment of cervical or penile cancer. Previous reports suggested possible mechanisms in the development of lympha...

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Autores principales: Yoshida, Saaya, Fujimura, Taku, Ohuchi, Kentaro, Kambayashi, Yumi, Segawa, Yuichiro, Yamazaki, Emi, Tono, Hisayuki, Takahashi, Toshiya, Tsuchiyama, Kenichiro, Aiba, Setsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250377/
https://www.ncbi.nlm.nih.gov/pubmed/32508617
http://dx.doi.org/10.1159/000506975
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author Yoshida, Saaya
Fujimura, Taku
Ohuchi, Kentaro
Kambayashi, Yumi
Segawa, Yuichiro
Yamazaki, Emi
Tono, Hisayuki
Takahashi, Toshiya
Tsuchiyama, Kenichiro
Aiba, Setsuya
author_facet Yoshida, Saaya
Fujimura, Taku
Ohuchi, Kentaro
Kambayashi, Yumi
Segawa, Yuichiro
Yamazaki, Emi
Tono, Hisayuki
Takahashi, Toshiya
Tsuchiyama, Kenichiro
Aiba, Setsuya
author_sort Yoshida, Saaya
collection PubMed
description Stewart-Treves syndrome (STS) is a rare cutaneous lymphangiosarcoma developing from chronic lymph edema as a consequence of radical mastectomy or surgical invasion of the groin for the treatment of cervical or penile cancer. Previous reports suggested possible mechanisms in the development of lymphangiosarcoma that correlate with the immunological background of STS patients. In this report, we described two cases of STS developing in patients who underwent radical dissection for cervical cancer, we employed immunohistochemical staining of IL-23 and IL-17.
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spelling pubmed-72503772020-06-04 IL-23 Expression in Stewart-Treves Syndrome: Two Case Reports and Immunohistochemical Investigation Yoshida, Saaya Fujimura, Taku Ohuchi, Kentaro Kambayashi, Yumi Segawa, Yuichiro Yamazaki, Emi Tono, Hisayuki Takahashi, Toshiya Tsuchiyama, Kenichiro Aiba, Setsuya Case Rep Oncol Case Report Stewart-Treves syndrome (STS) is a rare cutaneous lymphangiosarcoma developing from chronic lymph edema as a consequence of radical mastectomy or surgical invasion of the groin for the treatment of cervical or penile cancer. Previous reports suggested possible mechanisms in the development of lymphangiosarcoma that correlate with the immunological background of STS patients. In this report, we described two cases of STS developing in patients who underwent radical dissection for cervical cancer, we employed immunohistochemical staining of IL-23 and IL-17. S. Karger AG 2020-04-30 /pmc/articles/PMC7250377/ /pubmed/32508617 http://dx.doi.org/10.1159/000506975 Text en Copyright © 2020 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Case Report
Yoshida, Saaya
Fujimura, Taku
Ohuchi, Kentaro
Kambayashi, Yumi
Segawa, Yuichiro
Yamazaki, Emi
Tono, Hisayuki
Takahashi, Toshiya
Tsuchiyama, Kenichiro
Aiba, Setsuya
IL-23 Expression in Stewart-Treves Syndrome: Two Case Reports and Immunohistochemical Investigation
title IL-23 Expression in Stewart-Treves Syndrome: Two Case Reports and Immunohistochemical Investigation
title_full IL-23 Expression in Stewart-Treves Syndrome: Two Case Reports and Immunohistochemical Investigation
title_fullStr IL-23 Expression in Stewart-Treves Syndrome: Two Case Reports and Immunohistochemical Investigation
title_full_unstemmed IL-23 Expression in Stewart-Treves Syndrome: Two Case Reports and Immunohistochemical Investigation
title_short IL-23 Expression in Stewart-Treves Syndrome: Two Case Reports and Immunohistochemical Investigation
title_sort il-23 expression in stewart-treves syndrome: two case reports and immunohistochemical investigation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250377/
https://www.ncbi.nlm.nih.gov/pubmed/32508617
http://dx.doi.org/10.1159/000506975
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