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A bruise-like patch in a 4-year-old girl
Y N Lau1, A G Affleck, S L Edwards
1Ninewells Hospital and Medical School.
Dermatology Online Journal
|September 21, 2013
Summary
Dermatofibrosarcoma protuberans (DFSP) in children can mimic vascular malformations, delaying diagnosis. A modified Mohs Micrographic Surgery (MMS) offers a viable treatment option, examining all margins for this rare pediatric sarcoma.
Area of Science:
- Pediatric Oncology
- Surgical Pathology
- Dermatology
Background:
- Dermatofibrosarcoma protuberans (DFSP) is a rare, locally invasive sarcoma with a high recurrence rate.
- In children, DFSP may present atypically, resembling vascular malformations, leading to diagnostic delays.
- While Mohs Micrographic Surgery (MMS) is standard for adult DFSP, its application in children is limited by prolonged anesthesia concerns.
Observation:
- A case study of a 4-year-old girl diagnosed with DFSP is presented.
- The patient underwent a modified MMS procedure.
- This approach involved two shorter general anesthetic sessions.
Findings:
- The modified MMS allowed for complete examination of peripheral and deep margins.
- This technique potentially addresses the challenge of extensive subclinical extensions in pediatric DFSP.
- The modified approach balances the benefits of MMS with reduced anesthetic burden.
Implications:
- Modified MMS may be a suitable alternative for treating pediatric DFSP, ensuring complete tumor removal.
- This approach could improve outcomes for children with DFSP by minimizing recurrence risk.
- Further investigation into modified MMS protocols for pediatric sarcomas is warranted.
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