Lim E J, Peh S C
Department of Pathology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Singapore Med J. 2000 Jun;41(6):279-85.
47 patients with non-Hodgkin's lymphoma (NHL) were studied retrospectively to determine their marrow and blood changes at diagnosis.
The blood counts, blood films, marrow smears, trephine and tissue biopsies of patients at diagnosis were reviewed. The scheme proposed by the International Lymphoma Study Group (REAL) was utilised for lymphoma subclassification.
21.3% had lymphoblastic lymphoma, 21.3% had peripheral T-cell lymphoma (unspecified), 29.8% had diffuse large B-cell NHL, 10.6% had Burkitt's lymphoma and 17% had others. The incidences of anaemia, one or more abnormal counts, lymphocytopenia, increased marrow reticulin and marrow eosinophilia at diagnosis were 66%, 85.1%, 41.3%, 40.9% and 44.7% respectively. Marrow involvement was present in 46.8% of the patients, with diffuse infiltration noted in 71.4% of these cases. Abnormal counts and anaemia were common in all the NHL subtypes. In lymphoblastic lymphoma, the common haematological abnormalities were peripheral atypical lymphocytes and diffuse marrow involvement. In peripheral T-cell lymphoma (unspecified), common features were peripheral lymphocytopenia, increased marrow reticulin and eosinophilia. In diffuse large B-cell NHL, peripheral lymphocytopenia, peripheral myeloid precursors and/or nucleated red cells and marrow involvement were common. In Burkitt's lymphoma, diffuse marrow involvement and eosinophilia were common. No significant differences were noted between most of the haematological parameters of B and T-NHLs. In comparison with other reports, we recorded higher overall incidences of anaemia and diffuse marrow involvement, and a lower incidence of marrow infiltration in peripheral T-cell lymphoma (unspecified).
对47例非霍奇金淋巴瘤(NHL)患者进行回顾性研究,以确定其诊断时的骨髓和血液变化。
回顾患者诊断时的血细胞计数、血涂片、骨髓涂片、骨髓活检和组织活检。采用国际淋巴瘤研究组(REAL)提出的方案对淋巴瘤进行亚分类。
21.3%为淋巴母细胞淋巴瘤,21.3%为外周T细胞淋巴瘤(未特定),29.8%为弥漫性大B细胞NHL,10.6%为伯基特淋巴瘤,17%为其他类型。诊断时贫血、一项或多项血细胞计数异常、淋巴细胞减少、骨髓网硬蛋白增加和骨髓嗜酸性粒细胞增多的发生率分别为66%、85.1%、41.3%、40.9%和44.7%。46.8%的患者存在骨髓受累,其中71.4%的病例为弥漫性浸润。所有NHL亚型中血细胞计数异常和贫血都很常见。在淋巴母细胞淋巴瘤中,常见的血液学异常是外周非典型淋巴细胞和弥漫性骨髓受累。在外周T细胞淋巴瘤(未特定)中,常见特征是外周淋巴细胞减少、骨髓网硬蛋白增加和嗜酸性粒细胞增多。在弥漫性大B细胞NHL中,外周淋巴细胞减少、外周髓系前体细胞和/或有核红细胞以及骨髓受累很常见。在伯基特淋巴瘤中,弥漫性骨髓受累和嗜酸性粒细胞增多很常见。B和T-NHLs的大多数血液学参数之间未发现显著差异。与其他报告相比,我们记录的贫血和弥漫性骨髓受累的总体发生率较高,外周T细胞淋巴瘤(未特定)的骨髓浸润发生率较低。