RESUMO

Plasma Cell Leukemia is a very rare form of plasmocytic dyscrasia, whose clinical and pathological characteristics warrant its recognition as a distinct subentity. We report the case of a 60 years old man who presented a rapidly fatal acute plasma cell leukemia, with multiple osteolytic lesions, hipercalcemia, renal and cardiac failure.

Assuntos

Leucemia Plasmocitária/patologia , Doença Aguda , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Diagnóstico Diferencial , Humanos , Leucemia Plasmocitária/tratamento farmacológico , Masculino , Pessoa de Meia-Idade , Mieloma Múltiplo/patologia