Vitolo Umberto, Ferreri Andrés J M, Montoto Silvia
Hematology Unit, Azienda Ospedaliera S. Giovanni Battista Molinette, Turin, Italy.
Crit Rev Oncol Hematol. 2008 Jun;66(3):248-61. doi: 10.1016/j.critrevonc.2008.01.014. Epub 2008 Mar 21.
Follicular lymphomas constitute approximately 30% of all non-Hodgkin lymphomas. These lymphomas are characterized by at least partially follicular growth pattern, but diffuse areas may be present. The proportions of follicular or diffuse areas vary also from case to case, which seems to be associated with prognosis. Follicular lymphomas should not be divided into distinct subtypes, but rather shows a continuous gradation in the number of large cells. On the bases of this grading, three groups have been defined: grades 1-3. There is a consensus that grade 3 follicular lymphomas, namely grade 3b, should be discriminated from lower-grade cases. The cells of follicular lymphomas express surface immunoglobulin, more frequently IgM+/-IgD>IgG>IgA, B-cell-associated antigens, CD10+/-; they are CD5-, CD23-/+, CD43-, and CD11c-. Follicular lymphomas express bcl-2 proteins, which is useful in distinguishing reactive from neoplastic follicles. t(14;18) is present in 70-95% of follicular lymphomas, involving rearrangement of bcl-2 gene. Clinical behavior of follicular lymphomas is heterogeneous and differs according to the histologic grade and extension of disease. Moreover, the evaluation of these malignancies is conditioned by therapeutic decision, which is also determined by main prognostic factors. The International Prognostic Index for aggressive lymphomas is not optimal for follicular lymphomas. Conversely, the Italian Lymphoma Intergroup Index and, more recently, the Follicular Lymphoma International Prognostic Index (FLIPI), designed in pre-rituximab era, seem to correlate well with outcome. Several active therapeutic approaches from the "wait and watch" strategy to the allogeneic transplantation are available for management of patients with follicular lymphoma. Therapeutic decision is mostly conditioned by patient's characteristics, stage, histologic grade, tumor burden, and risk-predicting factors.
滤泡性淋巴瘤约占所有非霍奇金淋巴瘤的30%。这些淋巴瘤的特征是至少部分呈滤泡性生长模式,但也可能存在弥漫区域。滤泡或弥漫区域的比例因病例而异,这似乎与预后相关。滤泡性淋巴瘤不应分为不同的亚型,而是在大细胞数量上呈现连续的分级。基于这种分级,定义了三组:1-3级。目前已达成共识,即3级滤泡性淋巴瘤,即3b级,应与低级别病例区分开来。滤泡性淋巴瘤的细胞表达表面免疫球蛋白,更常见的是IgM+/-IgD>IgG>IgA,以及B细胞相关抗原,CD10+/-;它们CD5-、CD23-/+、CD43-和CD11c-。滤泡性淋巴瘤表达bcl-2蛋白,这有助于区分反应性滤泡和肿瘤性滤泡。70-95%的滤泡性淋巴瘤存在t(14;18),涉及bcl-2基因重排。滤泡性淋巴瘤的临床行为具有异质性,根据组织学分级和疾病范围而有所不同。此外,对这些恶性肿瘤的评估受治疗决策的制约,而治疗决策也由主要预后因素决定。侵袭性淋巴瘤的国际预后指数对滤泡性淋巴瘤并不适用。相反,意大利淋巴瘤协作组指数,以及最近在利妥昔单抗时代之前设计的滤泡性淋巴瘤国际预后指数(FLIPI),似乎与预后有很好的相关性。对于滤泡性淋巴瘤患者的管理,有几种从“观察等待”策略到异基因移植的积极治疗方法可供选择。治疗决策主要受患者特征、分期、组织学分级、肿瘤负荷和风险预测因素的制约。