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Eur J Dermatol ; 29(1): 39-44, 2019 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-30670369

RESUMO

BACKGROUND: CD8+ CD30+ primary cutaneous T-cell lymphomas (PCTCL) are rare entities with overlapping pathological features and variable outcome. OBJECTIVES: We sought to highlight the importance of correlation between pathological findings and clinical presentation for correct classification of the disease. MATERIALS & METHODS: Two cases of CD8+ CD30+ PCTCL were investigated. The first patient presented with a multiple necro-erythematous lesion of the limb and the second with a papulo-necrotic lesion of the eyelid. RESULTS: Despite a different clinical presentation, pathological findings were similar in both cases. Clinico-pathological correlation led to a diagnosis of primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma in the first case and primary cutaneous anaplastic large-cell lymphoma in the second. The first patient died shortly after diagnosis and the second is alive without recurrence. CONCLUSIONS: Clinico-pathological correlation is essential for the correct identification of these rare diseases.


Assuntos
Antígenos CD8/imunologia , Antígeno Ki-1/imunologia , Linfoma/patologia , Transtornos Linfoproliferativos/patologia , Neoplasias Cutâneas/patologia , Idoso , Evolução Fatal , Feminino , Humanos , Linfoma/imunologia , Transtornos Linfoproliferativos/imunologia , Pessoa de Meia-Idade , Prognóstico , Neoplasias Cutâneas/imunologia
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