Department of Pathology, City of Hope National Medical Center, Duarte, CA 91010, United States.
Leuk Res. 2010 Apr;34(4):475-82. doi: 10.1016/j.leukres.2009.07.034. Epub 2009 Aug 19.
CD30-positive anaplastic large cell lymphoma (ALCL) is a distinctive malignant large cell lymphoma of T-cell lineage, often presenting in lymph node or extranodal sites. ALCL cases with extensive bone marrow and peripheral blood involvement manifested as "leukemic phase" are extremely rare and the most of those cases reported are anaplastic large cell lymphoma kinase (ALK) positive ALCL in childhood population. Here we report four adult cases of ALK-negative ALCL with extensive bone marrow and peripheral blood involvement manifested as "leukemic phase". Circulating large lymphoma cells varied from 20 to 80% in peripheral blood and bone marrow biopsy showed various nodular or interstitial infiltrates. By reviewing the clinicopathologic data of previously reported ALCL cases with extensive bone marrow and peripheral blood involvement, there appears to be of large variations in regard to the patient's age, morphologic variants, immunophenotypic or genotypic characteristics of the disease. While most cases of ALCL with peripheral blood and bone marrow involvement were ALK-positive or carrying t(2;5) translocation, rare ALK-negative cases were also present. Leukemic ALCL patients usually have unfavourable prognosis, regardless of ALK expression.
CD30 阳性间变性大细胞淋巴瘤(ALCL)是一种独特的 T 细胞谱系恶性大细胞淋巴瘤,常发生于淋巴结或结外部位。广泛累及骨髓和外周血表现为“白血病期”的 ALCL 病例极为罕见,且大多数报道的病例为儿童人群中的间变性大细胞淋巴瘤激酶(ALK)阳性 ALCL。本文报道了 4 例 ALK 阴性 ALCL 广泛累及骨髓和外周血表现为“白血病期”的成人病例。外周血中循环的大淋巴瘤细胞占 20%至 80%不等,骨髓活检显示各种结节状或间质浸润。通过复习先前报道的广泛累及骨髓和外周血的 ALCL 病例的临床病理资料,发现患者的年龄、形态学变异、疾病的免疫表型或基因型特征存在很大差异。虽然大多数累及外周血和骨髓的 ALCL 病例为 ALK 阳性或携带 t(2;5)易位,但也存在少数 ALK 阴性病例。无论 ALK 表达如何,白血病性 ALCL 患者通常预后不良。