Published online by Cambridge University Press: 17 June 2025
Pseudolymphomas can be comprised of a prominent infiltrate of B cells, T cells, and even plasma cells. In these settings, they can mimic a lymphoproliferative process and immunohistochemistry plays an important role in excluding cutaneous lymphoma. B-cell pseudolymphomas or cutaneous lymphoid hyperplasia can mimic cutaneous follicle center cell lymphoma and primary cutaneous marginal zone B-cell lymphoma histopathologically. T-cell pseudolymphomas include a variety of inflammatory dermatoses that exhibit epidermotropism and can mimic a T-cell lymphoproliferative disorders such as mycosis fungoides. Some examples include lymphomatoid contact dermatitis, lymphomatoid drug eruption, follicular mucinosis, lupus erythematosus panniculitis, pigmented purpuric dermatosis, pityriasis lichenoides chronica/pityriasis lichenoides et varioliformis acuta, and pseudolymphomatous folliculitis. In some instances, the infiltrate is rich in plasma cells as in IgG4-related disease in the skin. Ultimately clinical pathologic correlation and sometimes the use of molecular studies will allow the classification of these entities.
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