Your browser doesn't support javascript.
loading
A Case of Prolonged Hypogammaglobulinemia after Rituximab-Containing Chemotherapy in a Patient with Lymphoma / 대한내과학회지
Korean Journal of Medicine ; : 357-362, 2014.
Article em Ko | WPRIM | ID: wpr-63185
Biblioteca responsável: WPRO
ABSTRACT
Rituximab, an anti-CD20 monoclonal antibody, is an effective target agent against the B lymphocytes in B-cell lymphoid malignancies and various lymphoproliferative diseases. Moreover, the toxicity of rituximab is less severe than that of conventional cytotoxic agents, which has promoted the widespread application of rituximab in the treatment of B-cell lymphoma. However, depletion of B lymphocytes by rituximab, which leads to secondary hypogammaglobulinemia, can cause deterioration of humoral immunity. Although immune reconstitution after hematopoietic stem cell transplantation is known to prevent prolonged hypogammaglobulinemia, very few cases of long-standing hypogammaglobulinemia have been reported. We report herein a case of prolonged hypogammaglobulinemia after rituximab-containing chemotherapy and splenectomy in a patient with non-Hodgkin's lymphoma and discuss the clinical significance and pathogenetic mechanism of this phenomenon with a literature review.
Assuntos
Palavras-chave
Texto completo: 1 Base de dados: WPRIM Assunto principal: Esplenectomia / Linfoma não Hodgkin / Linfócitos B / Linfoma de Células B / Deficiência de IgG / Transplante de Células-Tronco Hematopoéticas / Citotoxinas / Agamaglobulinemia / Tratamento Farmacológico / Imunidade Humoral Limite: Humans Idioma: Ko Revista: Korean Journal of Medicine Ano de publicação: 2014 Tipo de documento: Article
Texto completo: 1 Base de dados: WPRIM Assunto principal: Esplenectomia / Linfoma não Hodgkin / Linfócitos B / Linfoma de Células B / Deficiência de IgG / Transplante de Células-Tronco Hematopoéticas / Citotoxinas / Agamaglobulinemia / Tratamento Farmacológico / Imunidade Humoral Limite: Humans Idioma: Ko Revista: Korean Journal of Medicine Ano de publicação: 2014 Tipo de documento: Article