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Tuberculosis and Respiratory Diseases ; : 302-306, 2016.
Artículo en Inglés | WPRIM | ID: wpr-125737

RESUMEN

Systemic vasculitis involving the lung is a rare manifestation of myelodysplastic syndrome (MDS), and secondary vasculitis is considered to have poor prognosis. A 44-year-old man presented with fever and dyspnea of 1 month duration. A chest radiograph revealed bilateral multiple wedge shaped consolidations. In addition, the results of a percutaneous needle biopsy for non-resolving pneumonia were compatible with pulmonary vasculitis. Bone marrow biopsy was performed due to the persistence of unexplained anemia and the patient was diagnosed with MDS. We reported a case of secondary vasculitis presenting as non-resolving pneumonia, later diagnosed as paraneoplastic syndrome of undiagnosed MDS. The cytopenia and vasculitis improved after a short course of glucocorticoid treatment, and there was no recurrence despite the progression of underlying MDS.


Asunto(s)
Adulto , Humanos , Anemia , Biopsia , Biopsia con Aguja , Médula Ósea , Disnea , Fiebre , Pulmón , Síndromes Mielodisplásicos , Síndromes Paraneoplásicos , Neumonía , Pronóstico , Radiografía Torácica , Recurrencia , Vasculitis Sistémica , Vasculitis , Vasculitis Leucocitoclástica Cutánea
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