Clinical features of 16 cases of lymphoplasmacytic lymphoma/Waldenström macroglobulinemia / 中国实验血液学杂志
Journal of Experimental Hematology
; (6): 1494-1498, 2010.
Article
en Zh
| WPRIM
| ID: wpr-332331
Biblioteca responsable:
WPRO
ABSTRACT
In order to investigate the clinical manifestations, diagnosis, therapy and prognosis of lymphoplasmacytic lymphoma/Waldenström macroglobulinemia (LPL/WM), 16 patients with LPL/WM were analyzed retrospectively. The results showed that the average age of 16 patients with LPL/WM was 65.1 years old, the most common syndromes were anemia and hyperviscosity syndrome, bone marrows were composed of small lymphocyte, admixed with variable numbers of plasma cells and plasmacytoid lymphocytes. And lymph node biopsy revealed that most cells expressed B-cell-associated antigen. Among the 16 cases, complete remission was 25%, overall response rate (ORR) was 81.3%, overall survival time was 6 to 108 months. 3 patients died and survival rate was 81.3 %. It is concluded that the clinical course of LPL/WM is typically indolent. These patients can acquire remission in clinic, but can not be cured, some of them can transform into patients with more malignant lymphoma.
Texto completo:
1
Base de datos:
WPRIM
Asunto principal:
Patología
/
Terapéutica
/
Médula Ósea
/
Estudios Retrospectivos
/
Macroglobulinemia de Waldenström
/
Diagnóstico
Tipo de estudio:
Diagnostic_studies
/
Observational_studies
/
Prognostic_studies
Límite:
Adult
/
Aged
/
Aged80
/
Female
/
Humans
/
Male
Idioma:
Zh
Revista:
Journal of Experimental Hematology
Año:
2010
Tipo del documento:
Article