BEDNAR’S TUMOR – A RARE VARIANT OF DERMATOFIBROSARCOMA PROTUBERANS
Bednar’s tumor is a rare pigmented variant of dermatofibrosarcoma protuberans (DFSP)—a cutaneous sarcoma of low to intermediate malignancy, characterized by a tendency for local recurrence. Histologically, it is defined by the presence of spindle-shaped cells arranged in a storiform pattern and melanin-containing dendritic cells. Clinically, the lesions often resemble melanoma or other pigmented dermal tumors. We present the case of a 66-year-old male with a long-standing, asymptomatic pigmented lesion in the right subclavicular region. Histopathological examination confirmed the diagnosis of Bednar’s tumor based on its characteristic morphology and immunohistochemical profile: diffuse CD34 expression in spindle cells and S-100 positivity in melanin-laden components. Radical surgical excision with a 2 cm margin was performed. Follow-up over a two-year period revealed no evidence of recurrence or metastasis, as confirmed by PET/CT. This case highlights the importance of early diagnosis, immunohistochemical distinction from melanoma, and the need for a multidisciplinary approach in managing rare cutaneous sarcomas with atypical presentation.
Authors
- Stoyan Ivanov Pavlov (ORCID: https://orcid.org/0000-0003-1090-1403)
- Yavor Penev (ORCID: https://orcid.org/0009-0003-8173-7054)
Publication Details
- Journal
- Journal of IMAB - Annual Proceeding (Scientific Papers)
- Published
- 2025-10-08
- DOI
- https://doi.org/10.5272/jimab.2025314.6532
- Primary Topic
- Sarcoma Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00