Cargando…

Dermatofibrosarcoma- An uncommon entity, commonly mismanaged: a case report

INTRODUCTION & IMPORTANCE: Dermatofibrosarcoma protuberans (DFS) is a slow-growing, recurrent, cutaneous soft tissue sarcoma with low metastatic potential. It is not uncommon for DFS to get misdiagnosed and treated like commoner parietal wall swellings, viz., epidermal cysts, lipomas and fibroma...

Descripción completa

Detalles Bibliográficos
Autores principales: Tanwar, Paran, Singh, Amandeep, Pratap, Shaurya, Rattan, Amulya, Minhas, Satinder Singh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479619/
https://www.ncbi.nlm.nih.gov/pubmed/34563815
http://dx.doi.org/10.1016/j.ijscr.2021.106385
_version_ 1784576298726719488
author Tanwar, Paran
Singh, Amandeep
Pratap, Shaurya
Rattan, Amulya
Minhas, Satinder Singh
author_facet Tanwar, Paran
Singh, Amandeep
Pratap, Shaurya
Rattan, Amulya
Minhas, Satinder Singh
author_sort Tanwar, Paran
collection PubMed
description INTRODUCTION & IMPORTANCE: Dermatofibrosarcoma protuberans (DFS) is a slow-growing, recurrent, cutaneous soft tissue sarcoma with low metastatic potential. It is not uncommon for DFS to get misdiagnosed and treated like commoner parietal wall swellings, viz., epidermal cysts, lipomas and fibromas. Suboptimal management often leads to recurrence, which may be difficult to manage. CASE REPORT: A 33-year male was referred to us with a lump in his lower abdomen for 15 years, without any symptoms. The patient underwent medical management for 6 years, followed by excision. The swelling recurred four years later and progressed in size till the next 5 years. At our centre, the patient underwent imaging and aspiration cytology, which established diagnosis of DFS, followed by wide local excision. Biopsy was conclusive and margins negative. DISCUSSION: DFS presents commonly as an asymptomatic indurated plaque that slowly enlarges over months to years. Untreated, DFS can attain massive dimensions, producing the large “protuberant” nodules, and hence the name. In the current report, 15 years elapsed before the correct diagnosis was established. In this case, recurrence first appeared after four years of excision. The possibility of primary wound closure after wide excision decreases with every subsequent excision, and reconstructive options may not be readily available. CONCLUSION: The current report highlights a diagnostic delay of 15 years in a case of DFS. Asymptomatic, indolent nature combined with low awareness among community doctors contribute to delay in timely diagnosis. Community doctors should consider DFS as a differential in any long-standing, indolent, asymptomatic parietal wall swelling, especially with a history of recurrence.
format Online
Article
Text
id pubmed-8479619
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-84796192021-10-06 Dermatofibrosarcoma- An uncommon entity, commonly mismanaged: a case report Tanwar, Paran Singh, Amandeep Pratap, Shaurya Rattan, Amulya Minhas, Satinder Singh Int J Surg Case Rep Case Report INTRODUCTION & IMPORTANCE: Dermatofibrosarcoma protuberans (DFS) is a slow-growing, recurrent, cutaneous soft tissue sarcoma with low metastatic potential. It is not uncommon for DFS to get misdiagnosed and treated like commoner parietal wall swellings, viz., epidermal cysts, lipomas and fibromas. Suboptimal management often leads to recurrence, which may be difficult to manage. CASE REPORT: A 33-year male was referred to us with a lump in his lower abdomen for 15 years, without any symptoms. The patient underwent medical management for 6 years, followed by excision. The swelling recurred four years later and progressed in size till the next 5 years. At our centre, the patient underwent imaging and aspiration cytology, which established diagnosis of DFS, followed by wide local excision. Biopsy was conclusive and margins negative. DISCUSSION: DFS presents commonly as an asymptomatic indurated plaque that slowly enlarges over months to years. Untreated, DFS can attain massive dimensions, producing the large “protuberant” nodules, and hence the name. In the current report, 15 years elapsed before the correct diagnosis was established. In this case, recurrence first appeared after four years of excision. The possibility of primary wound closure after wide excision decreases with every subsequent excision, and reconstructive options may not be readily available. CONCLUSION: The current report highlights a diagnostic delay of 15 years in a case of DFS. Asymptomatic, indolent nature combined with low awareness among community doctors contribute to delay in timely diagnosis. Community doctors should consider DFS as a differential in any long-standing, indolent, asymptomatic parietal wall swelling, especially with a history of recurrence. Elsevier 2021-09-06 /pmc/articles/PMC8479619/ /pubmed/34563815 http://dx.doi.org/10.1016/j.ijscr.2021.106385 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Tanwar, Paran
Singh, Amandeep
Pratap, Shaurya
Rattan, Amulya
Minhas, Satinder Singh
Dermatofibrosarcoma- An uncommon entity, commonly mismanaged: a case report
title Dermatofibrosarcoma- An uncommon entity, commonly mismanaged: a case report
title_full Dermatofibrosarcoma- An uncommon entity, commonly mismanaged: a case report
title_fullStr Dermatofibrosarcoma- An uncommon entity, commonly mismanaged: a case report
title_full_unstemmed Dermatofibrosarcoma- An uncommon entity, commonly mismanaged: a case report
title_short Dermatofibrosarcoma- An uncommon entity, commonly mismanaged: a case report
title_sort dermatofibrosarcoma- an uncommon entity, commonly mismanaged: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479619/
https://www.ncbi.nlm.nih.gov/pubmed/34563815
http://dx.doi.org/10.1016/j.ijscr.2021.106385
work_keys_str_mv AT tanwarparan dermatofibrosarcomaanuncommonentitycommonlymismanagedacasereport
AT singhamandeep dermatofibrosarcomaanuncommonentitycommonlymismanagedacasereport
AT pratapshaurya dermatofibrosarcomaanuncommonentitycommonlymismanagedacasereport
AT rattanamulya dermatofibrosarcomaanuncommonentitycommonlymismanagedacasereport
AT minhassatindersingh dermatofibrosarcomaanuncommonentitycommonlymismanagedacasereport