# Bednar Tumor: A Rare Variant of Dermatofibrosarcoma Protuberans

**Authors:** Michelle Alcocer Salas, Diana L Vazquez-Cantu, Bryan Salvador Sol Tlapalamatl, Mercedes Hernández Torres, José Alfredo Soto-Ortiz

PMC · DOI: 10.7759/cureus.102955 · 2026-02-04

## TL;DR

This paper reports a rare case of a pigmented variant of dermatofibrosarcoma protuberans, known as Bednar tumor, emphasizing its clinical presentation and diagnostic approach.

## Contribution

The paper contributes a rare clinical case report of a Bednar tumor, highlighting its diagnostic challenges and clinical significance.

## Key findings

- The patient presented with a long-standing pigmented lesion that evolved into a neoplasm with specific clinical features.
- Histopathological and immunohistochemical analyses confirmed the diagnosis of Bednar tumor, a rare variant of DFSP.

## Abstract

Dermatofibrosarcoma protuberans (DFSP) is a rare dermal sarcoma of intermediate malignancy characterized by locally aggressive behavior and a low metastatic potential. The classic form typically presents as a slow-growing protuberant tumor involving the trunk or proximal extremities; however, several uncommon variants have been described. We report the case of a 32-year-old woman who presented with a long-standing pigmented lesion on the shoulder that had been present since childhood and showed progressive changes over the preceding six months. Clinically, the lesion evolved into an oval-shaped neoplasm with erythematous and brown pigmentation, a smooth surface, and an infiltrative consistency. Based on the clinical features, a diagnosis of DFSP was suspected, with particular consideration given to its rare pigmented variant, known as Bednar tumor. Histopathological examination and immunohistochemical analysis were performed to confirm the diagnosis and guide management. Although Bednar tumor exhibits distinctive histologic features due to the presence of melanin-producing dendritic cells, its biological behavior and prognosis are similar to those of conventional DFSP. Notably, only three cases of DFSP have been diagnosed over a 13-year period at a tertiary dermatology referral center in western Mexico, underscoring the rarity of this entity and the importance of clinical awareness for timely diagnosis and appropriate treatment.

## Linked entities

- **Diseases:** Dermatofibrosarcoma protuberans (MONDO:0011934), Bednar tumor (MONDO:0023273)

## Full-text entities

- **Genes:** COL1A1 (collagen type I alpha 1 chain) [NCBI Gene 1277] {aka CAFYD, EDSARTH1, EDSC, OI1, OI2, OI3}, PDGFB (platelet derived growth factor subunit B) [NCBI Gene 5155] {aka IBGC5, PDGF-2, PDGF2, SIS, SSV, c-sis}, CD34 (CD34 molecule) [NCBI Gene 947], F13A1 (coagulation factor XIII A chain) [NCBI Gene 2162] {aka F13A}, VIM (vimentin) [NCBI Gene 7431]
- **Diseases:** fibrous histiocytoma (MESH:D018219), sarcomatous (MESH:D018316), metastasis (MESH:D009362), Bednar Tumor (MESH:D018223), keloid (MESH:D007627), mesenchymal tumors (MESH:C535700), bleeding (MESH:D006470), lymphadenopathy (MESH:D008206), blue nevus (MESH:D018329), dermal sarcoma (MESH:D012509), pain (MESH:D010146), malignant melanoma (MESH:D008545), melanocytic lesions (MESH:D009508), spindle cell neoplasms (MESH:D002277), pigmentation (MESH:D010859), cancers (MESH:D009369)
- **Chemicals:** melanin (MESH:D008543), triamcinolone acetonide (MESH:D014222), Tlapalamatl (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12965016/full.md

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Source: https://tomesphere.com/paper/PMC12965016