Department of Histopathology, Hammersmith Hospital Campus, Imperial College Healthcare NHS Trust, London, & Imperial College London, UK.
Br J Haematol. 2011 Aug;154(4):466-70. doi: 10.1111/j.1365-2141.2011.08760.x. Epub 2011 Jul 2.
Haematogones are normal, maturing B-cell precursors. They can be confused with neoplastic immature lymphoid cells of B lymphoblastic leukaemia/lymphoma or B-cell acute lymphoblastic leukaemia (B-ALL). Though multi-colour flow-cytometry strategies for distinguishing haematogones from cells of B-ALL are well-described, similar strategies have not been determined for bone marrow trephine biopsies (BMTB). We revisited the morphological and immunohistochemical features (CD20, CD34, TdT and PAX5 expression) in 69 BMTB from 62 patients - 27 with excess haematogones; seven with residual B-ALL after therapy; 18 with no reported excess of haematogones or residual acute leukaemia on BMTB; and 17 diagnostic samples of B-ALL. The distinctive immunophenotypic pattern of BMTB with excess haematogones was of CD34, TdT, CD20 and PAX5 accounting for increasing proportions of cells in the order mentioned, whereas among B-ALL, the immunohistochemical pattern was of CD20, PAX5 and TdT accounting for an equal proportion of cells. Furthermore, among haematogones, the intensity of CD20 expression was extremely heterogeneous as compared to the neoplastic cells in CD20-positive B-ALL. The TdT-positive haematogones were generally small and uniform, while a certain degree of heterogeneity was noticed among neoplastic B-ALL cells. This study provides a practical strategy to distinguish haematogones from B-ALL cells in BMTB.
血幼粒细胞是正常的成熟 B 细胞前体。它们可能与 B 淋巴母细胞白血病/淋巴瘤或 B 细胞急性淋巴细胞白血病(B-ALL)的肿瘤性未成熟淋巴细胞混淆。虽然已经很好地描述了用于区分血幼粒细胞和 B-ALL 细胞的多色流式细胞术策略,但尚未确定用于骨髓活检(BMTB)的类似策略。我们重新研究了 62 例患者的 69 例 BMTB 的形态学和免疫组织化学特征(CD20、CD34、TdT 和 PAX5 的表达),其中 27 例有过多的血幼粒细胞;7 例经治疗后仍有残留的 B-ALL;18 例 BMTB 无报道的血幼粒细胞或残留急性白血病过多;17 例 B-ALL 诊断样本。过多血幼粒细胞的 BMTB 的独特免疫表型模式为 CD34、TdT、CD20 和 PAX5,按上述顺序代表越来越多的细胞,而在 B-ALL 中,免疫组织化学模式为 CD20、PAX5 和 TdT,代表细胞比例相等。此外,与 CD20 阳性的 B-ALL 中的肿瘤细胞相比,血幼粒细胞中 CD20 的表达强度极为不均匀。TdT 阳性的血幼粒细胞通常较小且均匀,而在肿瘤性 B-ALL 细胞中则注意到一定程度的异质性。这项研究提供了一种实用的策略,可用于区分 BMTB 中的血幼粒细胞和 B-ALL 细胞。