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Sebaceoma associated with seborrheic keratosis
Angel Fernandez-Flores1, José Antonio Manjón
1Servicio de Anatomia Patologica, Hospital El Bierzo, Ponferrada, Spain; dermatopathonline@gmail.com.
This study reports a rare case of sebaceoma co-occurring with seborrheic keratosis in a 69-year-old woman. Immunohistochemistry confirmed the absence of Muir-Torre syndrome, distinguishing it from similar conditions.
Area of Science:
- Dermatopathology
- Oncology
Background:
- Sebaceoma is a rare benign adnexal tumor originating from sebaceous glands.
- The co-occurrence of sebaceoma and seborrheic keratosis is exceptionally rare, with only one prior report in medical literature.
- Distinguishing these tumors is crucial for accurate diagnosis and management, particularly to rule out rare genetic syndromes.
Observation:
- A 69-year-old female presented with a multicolored plaque on her left breast.
- Dermatoscopy revealed a central orange area with globules, indicative of dilated glands, and a peripherally pigmented brown and gray region.
- Histopathology confirmed a central sebaceoma and peripheral seborrheic keratosis.
Findings:
- Histopathological examination confirmed the coexistence of sebaceoma and seborrheic keratosis within the same lesion.
- Immunohistochemical analysis for mismatch repair proteins (MSH6, MSH2, MLH1, PMS2) showed preserved nuclear expression.
- This preserved expression ruled out Muir-Torre syndrome, a condition associated with sebaceous neoplasms and colorectal cancer.
Implications:
- This case adds to the limited literature on the combined occurrence of sebaceoma and seborrheic keratosis.
- The findings underscore the importance of thorough histopathological and immunohistochemical evaluation in diagnosing rare skin neoplasms.
- Excluding Muir-Torre syndrome is critical for patient management and genetic counseling.
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