Department of Diagnostic Haematology, The Royal Melbourne Hospital, Parkville, Victoria, Australia.
J Clin Pathol. 2011 Jun;64(6):520-3. doi: 10.1136/jcp.2010.088591. Epub 2011 Apr 6.
Correlations between the marrow histopathology and clinical findings in Waldenström macroglobulinaemia (WM) are not well defined, and the pathophysiology of the plasma cell involvement is poorly understood. The authors used a standardised immunohistological approach to the enumeration of B lymphocyte and plasma cell compartments in the bone-marrow trephine to investigate associations between bone-marrow morphology and clinical/laboratory indices.
In 80 newly diagnosed, untreated cases of WM, the authors determined the degree and pattern of B lymphocyte (CD20+) and plasma cell (CD138+) infiltration in the bone-marrow trephine, as defined by immunohistochemistry, and correlated the disease in the marrow with components of the international scoring system for WM (age, serum IgM paraprotein level, haemoglobin, platelet count and β(2) microglobulin). Plasma cell clonality was assessed by κ and λ staining.
Serum IgM paraprotein concentration was related to the plasma cell burden in the bone marrow (coefficient 0.231, p<0.005), but not the B lymphocytic infiltrate. Overall lymphoplasmacytic disease burden weakly correlated with severity of anaemia (coefficient 0.236, p=0.055). In 28/28 evaluated cases, plasma cells exhibited light chain restriction that was concordant with both that of the B lymphocytic infiltrate and paraprotein.
Bone-marrow features, in particular the degree of plasma cell infiltration, correlate with IgM paraprotein concentration at diagnosis in WM. The plasma cell compartment in this condition appears to be part of the neoplastic clone. In WM, specific evaluation of the plasma cell compartment in the bone marrow at baseline and following therapy may be valuable.
瓦尔登斯特伦巨球蛋白血症(WM)骨髓组织病理学与临床发现之间的相关性尚未明确,浆细胞浸润的病理生理学也知之甚少。作者采用标准化免疫组织化学方法对骨髓活检中的 B 淋巴细胞和浆细胞区室进行计数,以研究骨髓形态与临床/实验室指标之间的关系。
在 80 例新诊断、未经治疗的 WM 患者中,作者通过免疫组织化学确定骨髓活检中 B 淋巴细胞(CD20+)和浆细胞(CD138+)浸润的程度和模式,并将骨髓中的疾病与 WM 的国际评分系统的组成部分(年龄、血清 IgM 副蛋白水平、血红蛋白、血小板计数和β2 微球蛋白)相关联。浆细胞克隆性通过κ和λ染色评估。
血清 IgM 副蛋白浓度与骨髓浆细胞负荷相关(系数 0.231,p<0.005),但与 B 淋巴细胞浸润无关。总体淋巴浆细胞疾病负担与贫血严重程度呈弱相关(系数 0.236,p=0.055)。在 28/28 例评估病例中,浆细胞表现出轻链限制,与 B 淋巴细胞浸润和副蛋白一致。
骨髓特征,特别是浆细胞浸润程度,与 WM 诊断时的 IgM 副蛋白浓度相关。该疾病的浆细胞区室似乎是肿瘤克隆的一部分。在 WM 中,在基线和治疗后对骨髓浆细胞区室进行特定评估可能具有价值。