Lilleyman J S, Britton J A, Laycock B J
J Clin Pathol. 1981 Jan;34(1):60-2. doi: 10.1136/jcp.34.1.60.
Blast cell morphology was assessed at diagnosis and subsequent bone marrow relapse in 33 unselected patients with lymphoblastic leukemia (ALL). Each marrow was classified 'blind' according to the French-American-British (FAB) criteria, and it was found that 19 of 24 (79%) patients initially typed as FAB L1 changed to FAB L2 during the course of their disease, but no patient made the reverse morphological change (p is less than 0.001). Five patients retained FAB L1 appearances; these included three of the four who had T-cell markers. One patient typed as FAB L3 did so consistently. This study indicates that FAB L2 ALL frequently emerges as a treatment-resistant offshoot of FAB L1 and provides further evidence that this marks a more aggressive form of the disease.
对33例未经挑选的淋巴细胞白血病(ALL)患者在诊断时及随后的骨髓复发时的原始细胞形态进行了评估。根据法国-美国-英国(FAB)标准对每份骨髓进行“盲法”分类,发现24例最初分型为FAB L1的患者中有19例(79%)在病程中转变为FAB L2,但没有患者出现相反的形态学改变(p<0.001)。5例患者保持FAB L1外观;其中包括4例有T细胞标志物的患者中的3例。1例分型为FAB L3的患者始终保持该分型。本研究表明,FAB L2 ALL常作为FAB L1的耐药分支出现,并进一步证明这标志着该疾病更具侵袭性的形式。