Evidence map›Paper›PMID 41324204›Full record

ArticlePediatric dermatology

Dermatofibrosarcoma Protuberans in Children: Favorable Outcomes Using Wide Local Excision.

Jawad Aqeel, Claire E Holtz, Grace A Osborne, Steven J Kasten, Kelly L Harms, Elisabeth A Pedersen

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Article in Pediatric dermatology. 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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1 · What the graph read from it

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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

6 authors.

Jawad AqeelDepartment of Dermatology, Division of Cutaneous Surgery and Oncology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Claire E HoltzCollege of Literature, Science, and the Arts, University of Michigan, Ann Arbor, Michigan, USA.
Grace A OsborneDepartment of Dermatology, Division of Pediatric Dermatology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Steven J KastenDepartment of Plastic Surgery, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Kelly L HarmsDepartment of Dermatology, Division of Cutaneous Surgery and Oncology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Elisabeth A PedersenDepartment of Dermatology, Division of Cutaneous Surgery and Oncology, University of Michigan Medical School, Ann Arbor, Michigan, USA.ORCID https://orcid.org/0000-0002-4356-4055

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDermatofibrosarcoma protuberans (DFSP) is a rare and locally aggressive cutaneous sarcoma. Surgical excision remains first-line therapy, including for pediatric patients. However, given the rarity of DFSP, specific treatment recommendations for children have not been well defined. To inform pediatric-specific management, we analyzed outcomes in a retrospective cohort of pediatric DFSP patients treated with wide local excision (WLE).

methodsA single-center retrospective review of clinical records from 2004 through 2024 was conducted evaluating patients < 20 years of age who were diagnosed with DFSP and underwent treatment with WLE. Patients were divided into two groups based on treatment with relatively narrow (< 2 cm) or standard margins (≥ 2 cm). Descriptive analyses were performed.

resultsA total of 17 pediatric DFSP patients underwent WLE. The mean surgical margin was 1.76 ± 0.54 cm, and 14 of 16 evaluable patients (87.5%) were treated with margins of 2 cm or less. Complete excision after one surgery was achieved in 76.5% of patients. No patients experienced local or distant recurrence, and none required adjuvant therapy. Interestingly, 64.7% (11/17) had documentation describing the lesion being first noted at or around the time of birth. For patients with over 60 months of follow-up, the 5-year recurrence-free survival, disease-specific survival, and overall survival were all 100%.

conclusionsWhen appropriately selected and performed, WLE with a 1-2 cm initial margin, followed by re-excision when needed to achieve clear margins, does not compromise survival or risk of recurrence and may be considered an effective treatment option in pediatric DFSP.

Indexed as

DermatofibrosarcomaSkin NeoplasmsAdolescentChildChild, PreschoolFemaleHumansInfantMaleMargins of ExcisionRetrospective StudiesTreatment Outcomedermatofibrosarcoma protuberansmarginspediatric dermatologywide local excision

Identifiers

PMID41324204
PMCPMC13051024

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