1. Indolent <scp>CD8</scp> + primary cutaneous T‐cell lymphoma involving the eyelid of an adolescent
- Author
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Kirby Taylor, Chad D. Housewright, Sophia J Hendrick, Andrew Siref, Lindsay M Bicknell, Jonathan H. Tsai, and Andrew N. Minzenmayer
- Subjects
Pathology ,medicine.medical_specialty ,Histology ,Proliferative index ,CD68 ,business.industry ,Not Otherwise Specified ,Dermatology ,medicine.disease ,Cutaneous lymphoma ,Pathology and Forensic Medicine ,Lymphoma ,medicine.anatomical_structure ,medicine ,Eyelid ,Differential diagnosis ,business ,CD8 - Abstract
Primary cutaneous acral CD8+ T-cell lymphoma (PCACTL) is currently a provisional entity defined as a rare cutaneous proliferation of atypical CD8+ lymphocytes that preferentially involves acral sites and has a good prognosis. We present a case of primary cutaneous CD8+ T-cell lymphoma involving the eyelid of an adolescent male. The case shares features with PCACTL, including indolent clinical behavior and expression of CD68 in a Golgi-associated dot-like pattern; however, other features differ significantly from PCACTL as currently defined by the World Health Organization (WHO). These features include ulceration, expression of CD56, granzyme B, and perforin, and a high proliferative index. Given these discrepancies, our case is currently best classified as a CD8+ primary cutaneous peripheral T-cell lymphoma, not otherwise specified. We review the differential diagnosis for this case and suggest expanding the definition of PCACTL. This article is protected by copyright. All rights reserved.
- Published
- 2021