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Updated: Jan 7, 2026

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Author Spotlight: Anterior HR-OCT as a Non-Invasive Tool for Characterizing Ocular Surface Squamous Neoplasia
Published on: August 9, 2024
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Large Nonosseous Preaxial Polydactyly: Unique Case With Vascular Proliferation and Subepidermal Bullae
Hunter Myles Rogoff1, John Paul Prodoehl2, Katie Lee3
1Department of Plastic and Reconstructive Surgery, Geisinger Medical Center, Danville, PA, USA.
Summary
Preaxial polydactyly (PPD) can present with unique phenotypes not covered by current classifications. This case highlights a soft-tissue-only PPD requiring consideration for updated classification systems.
Area of Science:
- Hand surgery
- Congenital anomalies
- Medical genetics
Background:
- Preaxial polydactyly (PPD) involves extra digits on the thumb side, with diverse presentations.
- Existing classification systems for PPD struggle to categorize all observed phenotypes.
- A rare, nonosseous PPD case is presented that falls outside current classifications.
Purpose of the Study:
- To report a unique case of preaxial polydactyly.
- To discuss the implications of this case for existing PPD classification systems.
- To advocate for the inclusion of this phenotype in future classifications.
Main Methods:
- Clinical presentation and surgical management of a rare PPD case.
- Pathological examination of the excised supernumerary digit.
- Literature review of similar PPD cases.
Main Results:
- Successful surgical excision of a large, nonosseous PPD.
- Pathology revealed a soft-tissue-only digit with vascular proliferation and subepidermal bullae.
- The case did not align with established PPD classification criteria.
Conclusions:
- This rare PPD phenotype necessitates inclusion in existing classification systems.
- Accurate classification aids in patient counseling and clinical decision-making.
- Further research and classification updates are needed for comprehensive PPD management.
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