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Bilateral pulmonary alveolar infiltrate and prostate tumour in a 54-year-old man
André A Figueiredo1, Guilherme Brandao, Leonardo C Dentz
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.
Abstract:
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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