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Cutaneous Keratocyst With D2-40 Immunoreactivity in Basal Cell Nevus Syndrome
Clare A Goggins1, Michele L Zerah2, Florencia Anatelli3
1Department of Dermatology, Georgetown University School of Medicine, Washington, DC.
The American Journal of Dermatopathology
|February 19, 2021
Summary
Basal cell nevus syndrome (BCNS) patients rarely develop cutaneous keratocysts. A BCNS patient’s keratocyst showed D2-40 immunoreactivity, suggesting a link to odontogenic keratocysts.
Area of Science:
- Dermatology
- Oncology
- Genetics
Background:
- Basal cell nevus syndrome (BCNS) is a genetic disorder associated with various tumors.
- Cutaneous cysts, especially epidermoid cysts, are common in BCNS.
- Cutaneous keratocysts are rare in the general population and exceptionally rare in BCNS patients.
Observation:
- This study reports a rare case of a BCNS patient with a cutaneous keratocyst.
- The cutaneous keratocyst exhibited D2-40 (podoplanin) immunoreactivity.
- This specific immunoreactivity is typically found in odontogenic keratocysts, not cutaneous ones.
Findings:
- The presence of D2-40 immunoreactivity in a cutaneous keratocyst of a BCNS patient is a novel observation.
- This finding challenges previous understanding of cutaneous keratocyst characteristics.
- The immunoreactivity pattern aligns with that of odontogenic keratocysts.
Implications:
- Cutaneous keratocysts in BCNS patients may share developmental origins with odontogenic keratocysts.
- This potential homology suggests similar invasive and growth behaviors.
- Further research into this relationship could impact BCNS management and treatment strategies.
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