CD4/CD8 double negative pagetoid reticulosis: a case report and literature review |
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Authors: | Nikki Mourtzinos Puja K. Puri Guanghua Wang Min‐Ling Liu |
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Affiliation: | 1. Department of Pathology, George Washington University Hospital, Washington, DC, USA;2. Department of Pathology, Duke University Medical Center, Durham, NC, USA;3. Department of Molecular Pathology, Armed Forces Institute of Pathology, Washington, DC, USA;4. Pathology and Laboratory Medicine Service, Veterans Affairs Medical Center, Washington, DC, USA |
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Abstract: | Pagetoid reticulosis is an indolent primary cutaneous T‐cell lymphoma. It typically presents as a solitary and slowly growing patch or plaque on the extremity, histologically characterized by an acanthotic epidermis infiltrated with atypical lymphocytes. Here, we present histological, immunophenotypical and molecular findings of a 29‐year‐old Jamaican man with bilateral wrist plaques. Histology showed marked acanthosis, hyperkeratosis and an intraepidermal infiltration consisting of large atypical lymphocytes. Immunohistochemical stains showed CD3 and CD5 positive T cells with significant loss of CD7, double negative CD4 and CD8 and strong positive CD30. Molecular analysis showed a monoclonal T‐cell receptor (TCR) gamma gene rearrangement. Review of the literature confirms that the immunophenotype of pagetoid reticulosis is variable with decreasing frequency of CD8+ cytotoxic/suppressor T cell, CD4+ helper T cell and least commonly CD4/CD8 double negative phenotypes. Although CD4/CD8 double negative phenotype appears to be associated with higher proliferation index, it does not appear to confer prognostic significance. Mourtzinos N, Puri PK, Guanghua W, Liu M‐L. CD4/CD8 double negative pagetoid reticulosis: a case report and literature review. |
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