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Leuk Lymphoma ; 44(6): 1049-52, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12854908

ABSTRACT

Hematological diseases are often accompanied by respiratory disorders. Pulmonary alveolar proteinosis (PAP) is a rare disease characterized by excessive accumulation of surfactant in the alveolar space. We describe a case of PAP complicated by myelofibrosis following essential thrombocythemia. The patient developed high fever, respiratory failure, and leuko-erythroblastosis during the progressive course of PAP. These symptoms were alleviated by prednisolone. The level of serum IL-6 was elevated when PAP was progressing rapidly. This may explain why the symptoms were alleviated by the steroids.


Subject(s)
Primary Myelofibrosis/diagnosis , Pulmonary Alveolar Proteinosis/complications , Thrombocythemia, Essential/etiology , Bone Marrow/pathology , Fatal Outcome , Female , Humans , Lung/pathology , Middle Aged , Prednisone/therapeutic use , Primary Myelofibrosis/complications , Primary Myelofibrosis/diagnostic imaging , Primary Myelofibrosis/pathology , Pulmonary Alveolar Proteinosis/diagnostic imaging , Pulmonary Alveolar Proteinosis/pathology , Thrombocythemia, Essential/pathology , Tomography, X-Ray Computed
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