The spectrum of chronic lymphoproliferative disorders in Chinese people
Open Access
- 1 July 1994
- Vol. 74 (1) , 174-181
- https://doi.org/10.1002/1097-0142(19940701)74:1<174::aid-cncr2820740128>3.0.co;2-0
Abstract
Background. Chronic lymphoproliferative disorders are considered rare in Oriental patients and are thought to constitute only 2% of all leukemias in these patients, compared to 20‐30% in Western patients. We conducted a retrospective analysis of Chinese patients with chronic lymphoproliferative disorders to define the frequency and spectrum of these disorders. Methods. A consecutive series of Chinese patients with leukemia and lymphoproliferative disorders seen at two regional hospitals in Hong Kong were analyzed retrospectively. The diagnosis of chronic lymphoproliferative disorders was based on morphologic and immunologic criteria proposed by the French‐American‐British Cooperative Study Group. Results. Sixty‐four Chinese patients with chronic lymphoproliferative disorders were identified, and these patients constituted 19% of a total of 342 cases of leukemia diagnosed in 3 years. Chronic lymphocytic leukemia was the most common form, occurring at a frequency of 12.5% of all leukemias. The clinicopathologic features of these patients were similar to those of Western patients, except that Chinese patients tended to present with more advanced (Rai's Stages III and IV; Binet's Stage C) and bulky (splenomegaly >9 cm) disease, and expressed λ light chain about six times more frequently. Other chronic lymphoproliferative disorders identified in this study included prolymphocytic leukemia, mantle zone lymphoma, hairy cell leukemia, splenic lymphoma with villous lymphocytes, large granular lymphocyte leukemia, and Sezary syndrome. The authors did not identify any case of human T‐cell lymphotropic virus‐I‐related lymphoproliferative disorders within the study period. Conclusion. In addition to providing the frequencies of various chronic lymphoproliferative disorders in southern Chinese people, this study also showed that these disorders no longer should be considered rare in this population. Inherent biologic differences between lymphoproliferative disorders in Chinese and Western patients also may exist.Keywords
This publication has 21 references indexed in Scilit:
- Population-Based Age- and Sex-Specific Incidence Rates in the 4 Main Types of LeukaemiaScandinavian Journal of Haematology, 2009
- Prognostic factors in chronic lymphocytic leukaemia: the importance of age, sex and response to treatment in survivalBritish Journal of Haematology, 1989
- Proposals for the classification of chronic (mature) B and T lymphoid leukaemias. French-American-British (FAB) Cooperative Group.Journal of Clinical Pathology, 1989
- Malignant lymphoma in Hawaii-Japanese: A retrospective morphologic surveyHematological Oncology, 1989
- Chronic Lymphocytic Leukemia: Recommendations for Diagnosis, Staging, and Response CriteriaAnnals of Internal Medicine, 1989
- Chronic lymphocytic leukemia in chinaAmerican Journal of Hematology, 1987
- Cancer Epidemics in the People's Republic of China 3 4JNCI Journal of the National Cancer Institute, 1978
- A clinical staging system for chronic lymphocytic leukemia.Prognostic significanceCancer, 1977
- Clinical staging of chronic lymphocytic leukemiaBlood, 1975
- Incidence of Leukaemia in Singapore, and Rarity of Chronic Lymphocytic Leukaemia in ChineseBMJ, 1960