Cargando…

Peculiar thousand leaves soft‐tissue mass: Elastofibroma dorsi

Elastofibroma dorsi is an uncommon benign soft‐tissue tumor with uncertain pathogenesis (Medicina (Kaunas), 2021; 57, 370). Surgical excision is the therapeutic option for symptomatic patients. A pathological study confirms the diagnosis after surgery. The prognosis is excellent with extremely rare...

Descripción completa

Detalles Bibliográficos
Autores principales: Limaiem, Faten, Baccouch, Seifeddine, Hajri, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842450/
https://www.ncbi.nlm.nih.gov/pubmed/35223009
http://dx.doi.org/10.1002/ccr3.5413
_version_ 1784651052465782784
author Limaiem, Faten
Baccouch, Seifeddine
Hajri, Mohamed
author_facet Limaiem, Faten
Baccouch, Seifeddine
Hajri, Mohamed
author_sort Limaiem, Faten
collection PubMed
description Elastofibroma dorsi is an uncommon benign soft‐tissue tumor with uncertain pathogenesis (Medicina (Kaunas), 2021; 57, 370). Surgical excision is the therapeutic option for symptomatic patients. A pathological study confirms the diagnosis after surgery. The prognosis is excellent with extremely rare recurrence cases (Anticancer Res, 2021, 41, 2211).
format Online
Article
Text
id pubmed-8842450
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-88424502022-02-24 Peculiar thousand leaves soft‐tissue mass: Elastofibroma dorsi Limaiem, Faten Baccouch, Seifeddine Hajri, Mohamed Clin Case Rep Clinical Images Elastofibroma dorsi is an uncommon benign soft‐tissue tumor with uncertain pathogenesis (Medicina (Kaunas), 2021; 57, 370). Surgical excision is the therapeutic option for symptomatic patients. A pathological study confirms the diagnosis after surgery. The prognosis is excellent with extremely rare recurrence cases (Anticancer Res, 2021, 41, 2211). John Wiley and Sons Inc. 2022-02-14 /pmc/articles/PMC8842450/ /pubmed/35223009 http://dx.doi.org/10.1002/ccr3.5413 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Clinical Images
Limaiem, Faten
Baccouch, Seifeddine
Hajri, Mohamed
Peculiar thousand leaves soft‐tissue mass: Elastofibroma dorsi
title Peculiar thousand leaves soft‐tissue mass: Elastofibroma dorsi
title_full Peculiar thousand leaves soft‐tissue mass: Elastofibroma dorsi
title_fullStr Peculiar thousand leaves soft‐tissue mass: Elastofibroma dorsi
title_full_unstemmed Peculiar thousand leaves soft‐tissue mass: Elastofibroma dorsi
title_short Peculiar thousand leaves soft‐tissue mass: Elastofibroma dorsi
title_sort peculiar thousand leaves soft‐tissue mass: elastofibroma dorsi
topic Clinical Images
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842450/
https://www.ncbi.nlm.nih.gov/pubmed/35223009
http://dx.doi.org/10.1002/ccr3.5413
work_keys_str_mv AT limaiemfaten peculiarthousandleavessofttissuemasselastofibromadorsi
AT baccouchseifeddine peculiarthousandleavessofttissuemasselastofibromadorsi
AT hajrimohamed peculiarthousandleavessofttissuemasselastofibromadorsi