An intra-abdominal desmoid tumor

Desmoid tumor is a very rare neoplasm which develops from fibroblasts. These tumors do not have the ability to metastasize, but they can cause significant morbidity and mortality by local invasion and they are prone to local recurrence. We present a case of an aggressive fibromatosis in a 28-year-ol...

Descripción completa

Detalles Bibliográficos
Autores principales: Petró, Mátyás, Silye, Annamária, Székely, András, Kovács, Ilona, Yi-Che, Chang C, Papp, Tamás
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7903839/
https://www.ncbi.nlm.nih.gov/pubmed/33747549
http://dx.doi.org/10.1177/2058460121992455
_version_ 1783654815847415808
author Petró, Mátyás
Silye, Annamária
Székely, András
Kovács, Ilona
Yi-Che, Chang C
Papp, Tamás
author_facet Petró, Mátyás
Silye, Annamária
Székely, András
Kovács, Ilona
Yi-Che, Chang C
Papp, Tamás
author_sort Petró, Mátyás
collection PubMed
description Desmoid tumor is a very rare neoplasm which develops from fibroblasts. These tumors do not have the ability to metastasize, but they can cause significant morbidity and mortality by local invasion and they are prone to local recurrence. We present a case of an aggressive fibromatosis in a 28-year-old male patient with no previous medical history. The tumor was in the retroperitoneum and eventually caused perforation of the coecum. During the operation, no metastasis was found; however, local lymphadenopathy was seen. After the surgical resection, no adjuvant therapy (radio or chemotherapy) was given to the patient and on follow-up (after three years), no recurrence was observed.
format Online
Article
Text
id pubmed-7903839
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-79038392021-03-18 An intra-abdominal desmoid tumor Petró, Mátyás Silye, Annamária Székely, András Kovács, Ilona Yi-Che, Chang C Papp, Tamás Acta Radiol Open Case Report Desmoid tumor is a very rare neoplasm which develops from fibroblasts. These tumors do not have the ability to metastasize, but they can cause significant morbidity and mortality by local invasion and they are prone to local recurrence. We present a case of an aggressive fibromatosis in a 28-year-old male patient with no previous medical history. The tumor was in the retroperitoneum and eventually caused perforation of the coecum. During the operation, no metastasis was found; however, local lymphadenopathy was seen. After the surgical resection, no adjuvant therapy (radio or chemotherapy) was given to the patient and on follow-up (after three years), no recurrence was observed. SAGE Publications 2021-02-22 /pmc/articles/PMC7903839/ /pubmed/33747549 http://dx.doi.org/10.1177/2058460121992455 Text en © The Foundation Acta Radiologica 2021 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Petró, Mátyás
Silye, Annamária
Székely, András
Kovács, Ilona
Yi-Che, Chang C
Papp, Tamás
An intra-abdominal desmoid tumor
title An intra-abdominal desmoid tumor
title_full An intra-abdominal desmoid tumor
title_fullStr An intra-abdominal desmoid tumor
title_full_unstemmed An intra-abdominal desmoid tumor
title_short An intra-abdominal desmoid tumor
title_sort intra-abdominal desmoid tumor
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7903839/
https://www.ncbi.nlm.nih.gov/pubmed/33747549
http://dx.doi.org/10.1177/2058460121992455
work_keys_str_mv AT petromatyas anintraabdominaldesmoidtumor
AT silyeannamaria anintraabdominaldesmoidtumor
AT szekelyandras anintraabdominaldesmoidtumor
AT kovacsilona anintraabdominaldesmoidtumor
AT yichechangc anintraabdominaldesmoidtumor
AT papptamas anintraabdominaldesmoidtumor
AT petromatyas intraabdominaldesmoidtumor
AT silyeannamaria intraabdominaldesmoidtumor
AT szekelyandras intraabdominaldesmoidtumor
AT kovacsilona intraabdominaldesmoidtumor
AT yichechangc intraabdominaldesmoidtumor
AT papptamas intraabdominaldesmoidtumor

Ejemplares similares