RESUMO
Plasma cells obtained from bone marrow samples of 45 patients with MM, eight patients with MGUS, eight patients with Waldenström's macroglobulinaemia (WM), one patient with immunocytoma, and 12 controls were characterized by immunophenotyping, estimation of DNA content, and labeling index, as well as by morphological analysis. Plasma cells from 37/45 myeloma and 5/8 MGUS patients expressed CD38 and CD56 (N-CAM) on their surface but were negative for other NK cell-associated antigens such as CD16 (Fc gamma RIII) or CD2. All tumor cells of less-differentiated cell type (WM, immunocytoma) and normal polyclonal plasma cells were negative for CD56. CD56-specific mRNA was demonstrated in myeloma cells by northern blot analysis. Another adhesion molecule, ICAM-1 (CD54), was found on plasma cells from all patients and controls examined. Coexpression of CD19 (1/45), CD20 (9/45), or CD33 (3/45) was rare and CD10 with CD14 was expressed by a small tumor cell subpopulation of only one myeloma patient. The individual pattern of surface marker expression was not associated with a special-type myeloma protein isotype, stage or status of disease, LI or histological classification; however, a correlation between CD56 expression or histological classification and DNA content of the tumor cells was found.
Assuntos
Imunofenotipagem , Mieloma Múltiplo/imunologia , Plasmócitos/imunologia , ADP-Ribosil Ciclase , ADP-Ribosil Ciclase 1 , Antígenos CD/análise , Antígenos de Diferenciação/análise , Antígenos de Diferenciação de Linfócitos T/análise , Medula Óssea/patologia , Antígeno CD56 , Moléculas de Adesão Celular/análise , Citoplasma/imunologia , Humanos , Imunoglobulinas/análise , Molécula 1 de Adesão Intercelular , Glicoproteínas de Membrana , Paraproteinemias/imunologia , Macroglobulinemia de Waldenstrom/imunologiaRESUMO
A case of bronchiolitis obliterans after prior inhalation of NO2 is described. The diagnosis was confirmed histologically following diagnostic thoracotomy and biopsy by means of pulmonary wedge resection. The clinical course of the case was compatible with the typical phases described in the literature, and the condition underwent complete remission following treatment with corticoids.