Primary Ewing’s sarcoma in a small intestine – a case report and review of the literature

BACKGROUND: Ewing’s sarcoma usually presents in paediatric patients with its primary location being bone tissue. Nevertheless, we present such an adult case which arises from the small intestine. We registered thirty one cases of such origin published so far excluding ours. CASE PRESENTATION: We rep...

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Autores principales: Kolosov, Andrej, Dulskas, Audrius, Pauza, Kastytis, Selichova, Veslava, Seinin, Dmitrij, Stratilatovas, Eugenijus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249351/
https://www.ncbi.nlm.nih.gov/pubmed/32450834
http://dx.doi.org/10.1186/s12893-020-00774-z
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author Kolosov, Andrej
Dulskas, Audrius
Pauza, Kastytis
Selichova, Veslava
Seinin, Dmitrij
Stratilatovas, Eugenijus
author_facet Kolosov, Andrej
Dulskas, Audrius
Pauza, Kastytis
Selichova, Veslava
Seinin, Dmitrij
Stratilatovas, Eugenijus
author_sort Kolosov, Andrej
collection PubMed
description BACKGROUND: Ewing’s sarcoma usually presents in paediatric patients with its primary location being bone tissue. Nevertheless, we present such an adult case which arises from the small intestine. We registered thirty one cases of such origin published so far excluding ours. CASE PRESENTATION: We report a case of 30 year old female who was admitted due to the persistent anaemia. Whole body computed tomography scan revealed abdominal mass in her left upper abdominal compartment. Surgery on the mass originating from jejunum was performed, although due to extremely complicated postoperative period and rapid dissemination no additional therapy had been performed. The tumour was positive for CD99, ERG, CD56, Synaptophysin, PanCK, Cam5.2. CONCLUSION: Extraosseus Ewing’s sarcoma is extremely rare entity, with poor prognosis.
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spelling pubmed-72493512020-06-04 Primary Ewing’s sarcoma in a small intestine – a case report and review of the literature Kolosov, Andrej Dulskas, Audrius Pauza, Kastytis Selichova, Veslava Seinin, Dmitrij Stratilatovas, Eugenijus BMC Surg Case Report BACKGROUND: Ewing’s sarcoma usually presents in paediatric patients with its primary location being bone tissue. Nevertheless, we present such an adult case which arises from the small intestine. We registered thirty one cases of such origin published so far excluding ours. CASE PRESENTATION: We report a case of 30 year old female who was admitted due to the persistent anaemia. Whole body computed tomography scan revealed abdominal mass in her left upper abdominal compartment. Surgery on the mass originating from jejunum was performed, although due to extremely complicated postoperative period and rapid dissemination no additional therapy had been performed. The tumour was positive for CD99, ERG, CD56, Synaptophysin, PanCK, Cam5.2. CONCLUSION: Extraosseus Ewing’s sarcoma is extremely rare entity, with poor prognosis. BioMed Central 2020-05-25 /pmc/articles/PMC7249351/ /pubmed/32450834 http://dx.doi.org/10.1186/s12893-020-00774-z Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Kolosov, Andrej
Dulskas, Audrius
Pauza, Kastytis
Selichova, Veslava
Seinin, Dmitrij
Stratilatovas, Eugenijus
Primary Ewing’s sarcoma in a small intestine – a case report and review of the literature
title Primary Ewing’s sarcoma in a small intestine – a case report and review of the literature
title_full Primary Ewing’s sarcoma in a small intestine – a case report and review of the literature
title_fullStr Primary Ewing’s sarcoma in a small intestine – a case report and review of the literature
title_full_unstemmed Primary Ewing’s sarcoma in a small intestine – a case report and review of the literature
title_short Primary Ewing’s sarcoma in a small intestine – a case report and review of the literature
title_sort primary ewing’s sarcoma in a small intestine – a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249351/
https://www.ncbi.nlm.nih.gov/pubmed/32450834
http://dx.doi.org/10.1186/s12893-020-00774-z
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