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Published 2 February 2009
Cite this as: BMJ Case Reports 2009 [doi:10.1136/bcr.09.2008.0888]
Copyright © 2009 by the BMJ Publishing Group Ltd.

Unusual association of diseases/symptoms

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

1 Universidade 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
2 Santa Casa de Misericórdia de Juiz de Fora, Rua Irineu Marinho 365, Juiz de Fora, Minas Gerais, 36021580, Brazil
3 CIDAP, Rua Irineu Marinho 365, Juiz de Fora, Minas Gerais, 36021580, Brazil
4 Centerq, Rua Irineu Marinho 365, Juiz de Fora, Minas Gerais, 36021580, Brazil

Correspondence to:
andreavaresef{at}gmail.com

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.


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