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Anais Brasileiros de Dermatologia

versión impresa ISSN 0365-0596versión On-line ISSN 1806-4841

Resumen

VALENTIM, Flávia de Oliveira; OLIVEIRA, Cristiano Claudino  y  MIOT, Hélio Amante. Case for diagnosis. Primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder. An. Bras. Dermatol. [online]. 2019, vol.94, n.1, pp.99-101. ISSN 1806-4841.  http://dx.doi.org/10.1590/abd1806-4841.20198513.

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.

Palabras clave : Lymphoma; Lymphoproliferative disorders; Pseudolymphoma.

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