Smadja N, Krulik M, Louvet C, de Gramont A, Gonzalez-Canali G, Mougeot-Martin M
Laboratoire de Cytogénétique Hémato-Cancérologique, Hôpital Saint-Antoine, Paris, France.
Cancer Genet Cytogenet. 1991 Mar;52(1):123-9. doi: 10.1016/0165-4608(91)90062-y.
Plasma cell leukemia (PCL) is a very rare disease. We report two cases of PCL with complex chromosomal abnormalities: long arm trisomy and short arm partial monosomy of chromosome 1, a marker derived from chromosome 8, and monosomy 13 were found in both cases; other additional chromosome abnormalities were also present in each case. Bastard et al. reports two similar cases in this issue. Cytogenetic studies in PCL have seldom been reported in the literature: chromosomal abnormalities are most often complex: chromosomes 1, 8, 11, 13, and 14 are those most frequently involved. Such cytogenetic findings are observed in advanced multiple myeloma. Cytogenetic, clinical, and immunological findings observed in PCL and the advanced stage of multiple myeloma are arguments for the single origin of pathogenesis.
浆细胞白血病(PCL)是一种非常罕见的疾病。我们报告了两例伴有复杂染色体异常的PCL病例:两例均发现1号染色体长臂三体和短臂部分单体、一条源自8号染色体的标记染色体以及13号染色体单体;每例还存在其他额外的染色体异常。巴斯塔德等人在本期报道了两例类似病例。关于PCL的细胞遗传学研究在文献中鲜有报道:染色体异常最常较为复杂,1、8、11、13和14号染色体是最常受累的染色体。在晚期多发性骨髓瘤中也观察到此类细胞遗传学结果。在PCL和晚期多发性骨髓瘤中观察到的细胞遗传学、临床和免疫学结果支持发病机制单一起源的观点。