Primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder is a rare
disease, with an indolent evolution and benign course. The classic presentation
is a solitary nodule on the face or trunk. The disorder’s rarity and clinical
and histopathological characteristics, can make the diagnosis difficult. We
present the case of a 36-year-old Caucasian woman with a purplish erythematous
nodule, hardened, shiny, asymptomatic, on the left nasal ala, which had grown
progressively for 45 days. Histopathological examination and
immunohistochemistry panel demonstrated alterations consistent with primary
cutaneous CD4+ small/medium T-cell lymphoproliferative disorder. There was
complete remission of the condition within 60 days of treatment with potent
occlusive corticosteroids.