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Solitary CD8-Positive Primary Cutaneous Peripheral T-Cell Lymphoma: A Question of Classification
Inês Rolim1, Arti BakShi2, Elizabeth West3
1Anatomic Pathology Service, Champalimaud Clinical Centre (CCC), Lisbon, Portugal.
Insights
This case study discusses a rare skin lymphoma with unusual features. The diagnosis favored peripheral T-cell lymphoma, not otherwise specified, over acral CD8(+) lymphoma.
Area of Science:
- Dermatopathology
- Hematopathology
- Oncology
Background:
- Acral CD8(+) lymphoma is a provisional entity in the WHO Lymphoma Classification.
- It is characterized by a specific dot-like CD68 immunohistochemical expression.
- This entity is typically associated with acral (extremity) skin sites.
Observation:
- A solitary, ulcerated cutaneous lesion on the forehead of an adult male was analyzed.
- The lesion exhibited a CD8(+) cytotoxic phenotype.
- Areas of dot-like CD68 positivity were observed, mimicking acral CD8(+) lymphoma.
Findings:
- The forehead location and other features deviated from the classical description of acral CD8(+) lymphoma.
- Immunohistochemical analysis revealed a CD8(+) cytotoxic T-cell phenotype.
- The pattern of CD68 positivity, while dot-like in areas, was not entirely typical.
Implications:
- The case highlights diagnostic challenges in cutaneous lymphomas.
- It suggests that similar immunohistochemical findings can occur in non-acral sites.
- The preferred diagnosis of peripheral T-cell lymphoma, not otherwise specified, broadens the differential diagnosis for such lesions.
Abstract:
Acral CD8(+) lymphoma is a provisional entity in the latest edition of the WHO Lymphoma Classification and is associated with a highly specific dot-like pattern of immunohistochemical expression of CD68. We report a case of an ulcerated solitary cutaneous lesion arising on the forehead of an adult man, which had a CD8(+) cytotoxic phenotype and areas of dot-like CD68 positivity, but with a number of features that significantly detracted from the classically described acral CD8(+) lymphoma. The nosological status of the lesion is discussed with respect to a preferred diagnosis of peripheral T-cell lymphoma, not otherwise specified.
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