Vaswani Preeti Prerna M, Dumagay Teresita E
Section of Hematology, Department of Internal Medicine, Philippine General Hospital, University of the Philippines Manila, Manila, Philippines.
BMJ Case Rep. 2018 Aug 20;2018:bcr-2018-226006. doi: 10.1136/bcr-2018-226006.
Trisomy 5 as the sole cytogenetic aberration in acute lymphoblastic leukaemia (ALL) is exceedingly rare. As such, its prognostic and therapeutic relevance remains unknown. We report a case of an 18-year-old young man who was diagnosed with B cell ALL with trisomy 5 as the sole chromosomal abnormality. He was treated with chemotherapy and went into complete remission. On the 14th month of treatment, he relapsed with central nervous system involvement characterised by leukaemic infiltration of the optic nerve and facial palsy. He subsequently underwent reinduction chemotherapy with aggressive intrathecal chemotherapy followed by posterior globe and whole brain radiation therapy. He is currently on his 26th month of treatment, in second remission, with complete resolution of leukaemic infiltrative optic neuropathy and facial paralysis. As more cases of this nature are reported, we will be able to determine the relevance of this distinct cytogenetic entity.
5号染色体三体作为急性淋巴细胞白血病(ALL)唯一的细胞遗传学异常极为罕见。因此,其预后及治疗相关性仍不明确。我们报告一例18岁青年男性,被诊断为B细胞ALL,5号染色体三体是唯一的染色体异常。他接受了化疗并实现完全缓解。在治疗的第14个月,他复发,伴有中枢神经系统受累,表现为视神经白血病浸润和面瘫。随后,他接受了强化鞘内化疗的再诱导化疗,接着进行了眼球后部和全脑放射治疗。他目前处于治疗的第26个月,处于第二次缓解期,白血病浸润性视神经病变和面瘫已完全消退。随着更多此类病例的报告,我们将能够确定这种独特细胞遗传学实体的相关性。