Bilateral pulmonary alveolar infiltrate and prostate tumour in a 54-year-old man
- André A Figueiredo1,
- Guilherme Brandao2,
- Leonardo C Dentz3,
- Christiane M M Alves4,
- Antonio E S Stroppa2
- 1Universidade Federal de Juiz de Fora, Morphology and Urology, Rua Irineu Marinho 365 Apto 801 - Bloco 3, Bom Pastor, Juiz de Fora MG, CEP 36021–58, Brazil
- 2Santa Casa de Misericórdia de Juiz de Fora, Rua Irineu Marinho 365, Juiz de Fora, Minas Gerais, 36021580, Brazil
- 3CIDAP, Rua Irineu Marinho 365, Juiz de Fora, Minas Gerais, 36021580, Brazil
- 4Centerq, Rua Irineu Marinho 365, Juiz de Fora, Minas Gerais, 36021580, Brazil
- andreavaresef{at}gmail.com
- Published 2 February 2009
Summary
This case study describes the association between two rare entities: pulmonary alveolar proteinosis (PAP) and embryonic rhabdomyosarcoma of the prostate in a 54 year old male presenting with pulmonary symptoms and obstructive urinary symptoms. The prostate tumour was treated with a radical cystectomy and adjuvant chemotherapy and radiotherapy. The patient did not wish to have treatment for his pulmonary disease and died 1 year after surgery as a result of intra-abdominal spread of the neoplasm.
Footnotes
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Competing interests: None.








