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A Case of Pulmonary Intravascular Lymphomatosis / 결핵
Tuberculosis and Respiratory Diseases ; : 1390-1395, 1997.
Artículo en Coreano | WPRIM | ID: wpr-148572
ABSTRACT
Intravascular lymphomatosis(IVL) which was first described by pfleger and Tappeiner in 1959 is rare malignancy characterized by neoplastic proliferation of lymphoid cell lineage within the vascular lumen with little or no adjacent parenchymal involvement. Its usual sites of involvement are central nervous system and skin or infrequently heart, lungs, pancreas, liver, spleen, kidney, adrenal glands, genitourinary tract, and bone marrow. Pulmonary involvement of IVL is not common. Symptoms of pulmonary involvement include dyspnea, cough and fever. Radiologicially, the disease is manifested with diffuse interstitial infiltrates. We report a recently experienced case of pulmonary intravascular lymphomatosis which was manifested with fever and chest pain.
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Páncreas / Piel / Bazo / Médula Ósea / Dolor en el Pecho / Linfocitos / Sistema Nervioso Central / Glándulas Suprarrenales / Tos / Disnea Idioma: Coreano Revista: Tuberculosis and Respiratory Diseases Año: 1997 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Páncreas / Piel / Bazo / Médula Ósea / Dolor en el Pecho / Linfocitos / Sistema Nervioso Central / Glándulas Suprarrenales / Tos / Disnea Idioma: Coreano Revista: Tuberculosis and Respiratory Diseases Año: 1997 Tipo del documento: Artículo