Primary B cell lymphoma of the mediastinum

✍ Scribed by C. S. Chim; Raymond Liang; A. C. L. Chan; Y. L. Kwong; F. C. S. Ho; David Todd

• Publisher: John Wiley and Sons
• Year: 1996
• Tongue: English
• Weight: 471 KB
• Volume: 14
• Category: Article
• ISSN: 0278-0232
• DOI: 10.1002/(sici)1099-1069(199612)14:4<173::aid-hon588>3.0.co;2-w

✦ Synopsis

Primary B cell mediastinal lymphoma has been recognized as a distinct entity recently. This is a retrospective study to define the clinical features and treatment outcome over a 10-year period. Twenty-four consecutive patients (male/female: 11/13) with B cell lymphoma primarily involving the mediastinum were studied. The median age was 34 years. Symptoms were mainly referrable to the chest, with superior vena cava syndrome (SVCO) present in one-third of the patients. Bulky disease was present in over half (58 per cent) and B symptoms were present in 38 per cent of patients. The overall CR rate was 70 per cent and the 5-year 0s rates were 56 per cent and 72 per cent for all and CR patients respectively.

Five (71 per cent) primary refractory patients and four (66 per cent) relapsed patients died despite salvage therapy. Six relapses occurred at a median of 6 months from treatment. This study showed that primary large B cell lymphoma of the mediastinum is a clinically distinct entity affecting young patients. A significant proportion attained CR and overall, more than half achieved prolonged remission, and most of the relapses occurred early. However, those who failed to attain CR or relapsed still had a poor outcome. An intensive therapy such as autologous bone marrow transplant has to be considered in this subgroup of patients. ! ( j 1996 by John Wiley & Sons, Ltd.