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.