Linfoma pulmonar primário – a propósito de um caso clínico

Autores

  • Carla Gil Serviço de Medicina Interna do Hospital de Tomar, Centro Hospitalar do Médio Tejo
  • Carolina Correia Serviço de Medicina Interna do Hospital de Tomar, Centro Hospitalar do Médio Tejo
  • Edgar Pereira Serviço de Medicina Interna do Hospital de Tomar, Centro Hospitalar do Médio Tejo

Palavras-chave:

Linfoma pulmonar, BALT, MALT

Resumo

Descreve-se o caso de uma doente de 64 anos de idade que se
apresentou no Serviço de Urgência com queixas de tosse irritativa,
astenia intensa e perda ponderal não quantificada, com cerca de
dois meses de evolução. Dos antecedentes pessoais destaca-se
artrite reumatóide, em remissão há vários anos. A radiografia
torácica evidenciava uma massa ovóide no hilo esquerdo. Foi
só após a segunda broncofi broscopia com biopsia e exame
anatomopatológico que se chegou ao diagnóstico de linfoma
pulmonar primário.
Os linfomas pulmonares primários são raros. A forma mais
habitual de apresentação é o linfoma B não-Hodgkin da zona
marginal, extranodal, originado no tecido linfóide associado à
mucosa brônquica (BALT - Bronchus Associated Lymphoid Tissue),
também denominado linfoma pulmonar primário do tipo MALT
(Mucosa Associated Lymphoid Tissue).

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Ficheiros Adicionais

Publicado

29-09-2006

Como Citar

1.
Gil C, Correia C, Pereira E. Linfoma pulmonar primário – a propósito de um caso clínico. RPMI [Internet]. 29 de Setembro de 2006 [citado 5 de Novembro de 2024];13(3):189-96. Disponível em: https://revista.spmi.pt/index.php/rpmi/article/view/1646

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