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Desmoplastic Small Round Cell Tumor of the Uterus: A Report of Molecularly Confirmed Case with EWSR1-WT1 Fusion

We report a case of a 49-year-old female with desmoplastic small round cell tumor of the uterus (DSRCT). Histologically, in some areas the tumor showed typical features with ample desmoplastic stroma, while in other areas the tumor cells diffusely infiltrated myometrium with only focal desmoplastic...

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Autores principales: Dundr, Pavel, Drozenová, Jana, Matěj, Radoslav, Bártů, Michaela, Němejcová, Kristýna, Robová, Helena, Rob, Lukáš, Hojný, Jan, Stružinská, Ivana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140206/
https://www.ncbi.nlm.nih.gov/pubmed/35626339
http://dx.doi.org/10.3390/diagnostics12051184
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author Dundr, Pavel
Drozenová, Jana
Matěj, Radoslav
Bártů, Michaela
Němejcová, Kristýna
Robová, Helena
Rob, Lukáš
Hojný, Jan
Stružinská, Ivana
author_facet Dundr, Pavel
Drozenová, Jana
Matěj, Radoslav
Bártů, Michaela
Němejcová, Kristýna
Robová, Helena
Rob, Lukáš
Hojný, Jan
Stružinská, Ivana
author_sort Dundr, Pavel
collection PubMed
description We report a case of a 49-year-old female with desmoplastic small round cell tumor of the uterus (DSRCT). Histologically, in some areas the tumor showed typical features with ample desmoplastic stroma, while in other areas the tumor cells diffusely infiltrated myometrium with only focal desmoplastic reaction. Immunohistochemically, the tumor cells showed diffuse positivity for desmin, CD56, CD57, EMA and cyclin D1. Focal positivity was present for antibodies against cytokeratin AE1/3, BerEP4, NSE, IFITM1 and CD10. The WT-1 antibody (against the N-terminus) showed cytoplasmic positivity in some tumor cells, while the nuclei were negative. P53 expression was wild-type. The Ki-67 index (MIB1 antibody) was about 55%. Other markers examined including transgelin, myogenin, synaptophysin, chromogranin, h-caldesmon, PAX8, and CD117 were all negative. NGS analysis revealed a fusion transcript of the EWSR1 and WT1 genes. DSRCT of the uterus is a rare neoplasm, as only two cases have been reported so far. However, only one of these cases was examined molecularly with a confirmation of the characteristic EWSR1-WT1 fusion. We report a second case of molecularly confirmed DSRCT of the uterus and discuss its clinical features, differential diagnosis and the significance of molecular testing.
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spelling pubmed-91402062022-05-28 Desmoplastic Small Round Cell Tumor of the Uterus: A Report of Molecularly Confirmed Case with EWSR1-WT1 Fusion Dundr, Pavel Drozenová, Jana Matěj, Radoslav Bártů, Michaela Němejcová, Kristýna Robová, Helena Rob, Lukáš Hojný, Jan Stružinská, Ivana Diagnostics (Basel) Case Report We report a case of a 49-year-old female with desmoplastic small round cell tumor of the uterus (DSRCT). Histologically, in some areas the tumor showed typical features with ample desmoplastic stroma, while in other areas the tumor cells diffusely infiltrated myometrium with only focal desmoplastic reaction. Immunohistochemically, the tumor cells showed diffuse positivity for desmin, CD56, CD57, EMA and cyclin D1. Focal positivity was present for antibodies against cytokeratin AE1/3, BerEP4, NSE, IFITM1 and CD10. The WT-1 antibody (against the N-terminus) showed cytoplasmic positivity in some tumor cells, while the nuclei were negative. P53 expression was wild-type. The Ki-67 index (MIB1 antibody) was about 55%. Other markers examined including transgelin, myogenin, synaptophysin, chromogranin, h-caldesmon, PAX8, and CD117 were all negative. NGS analysis revealed a fusion transcript of the EWSR1 and WT1 genes. DSRCT of the uterus is a rare neoplasm, as only two cases have been reported so far. However, only one of these cases was examined molecularly with a confirmation of the characteristic EWSR1-WT1 fusion. We report a second case of molecularly confirmed DSRCT of the uterus and discuss its clinical features, differential diagnosis and the significance of molecular testing. MDPI 2022-05-10 /pmc/articles/PMC9140206/ /pubmed/35626339 http://dx.doi.org/10.3390/diagnostics12051184 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Dundr, Pavel
Drozenová, Jana
Matěj, Radoslav
Bártů, Michaela
Němejcová, Kristýna
Robová, Helena
Rob, Lukáš
Hojný, Jan
Stružinská, Ivana
Desmoplastic Small Round Cell Tumor of the Uterus: A Report of Molecularly Confirmed Case with EWSR1-WT1 Fusion
title Desmoplastic Small Round Cell Tumor of the Uterus: A Report of Molecularly Confirmed Case with EWSR1-WT1 Fusion
title_full Desmoplastic Small Round Cell Tumor of the Uterus: A Report of Molecularly Confirmed Case with EWSR1-WT1 Fusion
title_fullStr Desmoplastic Small Round Cell Tumor of the Uterus: A Report of Molecularly Confirmed Case with EWSR1-WT1 Fusion
title_full_unstemmed Desmoplastic Small Round Cell Tumor of the Uterus: A Report of Molecularly Confirmed Case with EWSR1-WT1 Fusion
title_short Desmoplastic Small Round Cell Tumor of the Uterus: A Report of Molecularly Confirmed Case with EWSR1-WT1 Fusion
title_sort desmoplastic small round cell tumor of the uterus: a report of molecularly confirmed case with ewsr1-wt1 fusion
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140206/
https://www.ncbi.nlm.nih.gov/pubmed/35626339
http://dx.doi.org/10.3390/diagnostics12051184
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