Evidence map›Paper›PMID 42866317›Full record

ArticleAnnals of medicine and surgery (2012)2026

Unusual presentation of dermatofibrosarcoma protuberans in a young female: a rare case report and literature review.

Ankur Bhandari, Sabina Nhemafuki, Saurav Shah, Anil Mahato, Ujwal Sah, Sudikxya Basnet, Bishnu Prasad Ghimire

Abstract readCase Reports
In one paragraph

Article in Annals of medicine and surgery (2012), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Ankur BhandariDepartment of Dermatology, Manipal College of Medical Sciences, Pokhara, Nepal.ORCID https://orcid.org/0009-0001-4514-4484
Sabina NhemafukiDepartment of Dermatology, Manipal College of Medical Sciences, Pokhara, Nepal.
Saurav ShahDepartment of Medicine, Manipal College of Medical Sciences, Pokhara, Nepal.ORCID https://orcid.org/0009-0006-7509-4998
Anil MahatoDepartment of Medicine, Manipal College of Medical Sciences, Pokhara, Nepal.
Ujwal SahDepartment of Medicine, Manipal College of Medical Sciences, Pokhara, Nepal.ORCID https://orcid.org/0009-0000-7190-3547
Sudikxya BasnetDepartment of Pathology, Manipal College of Medical Sciences, Pokhara, Nepal.
Bishnu Prasad GhimireDepartment of Dermatology, Manipal College of Medical Sciences, Pokhara, Nepal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Dermatofibrosarcoma protuberans (DFSP) is a rare, low-grade malignant cutaneous soft tissue sarcoma of fibroblastic origin, characterized by slow but infiltrative growth and a high propensity for local recurrence, while distant metastasis remains uncommon. The reported incidence ranges from 0.8 to 5 cases per million population per year, accounting for less than 0.1% of all malignant tumors and approximately 1% of soft tissue sarcomas. Case presentation: The author reports a case of 33-year-old woman with no known comorbidities who presented to neuro OPD with complaint of solitary, dark-brown lump, associated with occasional pain over the lateral aspect of the elbow, for 7-8 months which was expanding gradually. Further on, the histopathological report revealed DFSP; wide local excision with vascular flap with split thickness skin graft of left elbow was therefore performed. Conclusion: DFSP is a rare cutaneous sarcoma with a high risk of local recurrence but excellent overall prognosis. Presentation at the elbow is uncommon and may delay diagnosis. This case emphasizes the importance of histopathological confirmation and adequate surgical excision with appropriate reconstruction. Long-term surveillance remains essential to detect recurrence early.

Indexed as

dermatofibrosarcoma protuberansMohsreciprocal translocationstoriform patternwide local excision

Identifiers

PMID42866317
PMCPMC13657506

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