Dermatofibrosarcoma is a rare cancer, accounting for 0.01% of all cancers. We here report the case of a 44-year-old female patient presenting with the 5 recurrence of locally advanced Darier-Ferrand dermatofibrosarcoma, that progressed on many cycles of neoadjuvant therapy and required emergency radiotherapy with good response. This allowed to perform wide excision of the tumor with healthy limits. The patient had remission after 1 year of follow-up. Prognosis for patients with Darier-Ferrand dermatofibrosarcoma is generally excellent. Wide surgery and the advent of Mohs surgery have improved local control. The role of radiotherapy is limited for non-resectable tumors or positive margins.
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http://dx.doi.org/10.11604/pamj.2022.41.234.22764 | DOI Listing |
Int J Surg Case Rep
July 2024
Pathology and Histology Department, Salah Azaiez Institute of Cancer, Tunis University of Medicine, University Tunis El Manar, Tunis, Tunisia.
Ann Chir Plast Esthet
January 2024
Service de chirurgie générale A, hôpital central de l'Armée-Dr-Mohamed-Seghir Nekkache, BP 244 Aïn-Naadja, Alger, Kouba, Algérie. Electronic address:
Introduction: Darrier-Ferrand dermatofibrosarcoma (DFSC) is the most common cutaneous sarcoma. It generally affects subjects with an average age of 40 years, without gender or race predominance. It is a tumour characterised by a slow evolution and local aggressiveness.
View Article and Find Full Text PDFInt J Surg Case Rep
July 2022
Department of Orthopedic, Homeland Security Forces Hospital La Marsa, United States of America.
Introduction And Importance: Darier-Ferrand dermatofibrosarcoma (DFS) is a rare mesenchymal tumor with an aggressive local behavior, high local recurrence frequency and low metastatic potential. It commonly presents as a raised slowly growing mass. It usually occurs on trunk and proximal extremities but rarely touches distal extremities such as hands, fingers, or foot below knees.
View Article and Find Full Text PDFPan Afr Med J
June 2022
Service de Radiothérapie, CHU Mohammed VI, Oujda, Maroc.
Dermatofibrosarcoma is a rare cancer, accounting for 0.01% of all cancers. We here report the case of a 44-year-old female patient presenting with the 5 recurrence of locally advanced Darier-Ferrand dermatofibrosarcoma, that progressed on many cycles of neoadjuvant therapy and required emergency radiotherapy with good response.
View Article and Find Full Text PDFPan Afr Med J
August 2021
Service de Chirurgie Générale, Sfax, Tunisie.
Dermatofibrosarcoma is a rare skin tumor. Morphological characteristics can be misleading and unknown to most of physicians. Diagnostic delay may affect patient´s management and prognosis.
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