Ali Saba F, Sonu Rebecca J, Dwyre Denis M, Jonas Brian A, Rashidi Hooman H
Department of Pathology and Laboratory Medicine, University of California Davis Medical Center, Sacramento, CA 95817, USA.
Department of Internal Medicine, Division of Hematology and Oncology, University of California Davis Medical Center, Sacramento, CA 95817, USA.
Case Rep Hematol. 2015;2015:318545. doi: 10.1155/2015/318545. Epub 2015 Dec 21.
Most myelodysplastic syndromes (MDS) present with loss or gain of chromosomal material and less commonly show translocations as a sole abnormality. In addition, certain translocations are more commonly seen in MDS than others, but to our knowledge, the presence of t(6;15) has not been reported in MDS, specifically therapy-related MDS (t-MDS) cases. Patients with t-MDS, a group of heterogeneous stem cell related disorders resulting as a latent complication of cytotoxic and/or radiation therapy, generally tend to have a poorer prognosis than de novo MDS. We present a unique case of a patient who initially presented with acute myeloid leukemia (AML) with a normal karyotype and FLT3-ITD and NPM1 mutations. The patient was successfully treated with chemotherapy and an autologous bone marrow transplant but subsequently developed a new FLT3-ITD negative t-MDS with a unique translocation, t(6;15)(q12;q15), three years after transplant. To our knowledge, this unique sole translocation has never been reported in MDS or t-MDS and given her successful response to treatment and remission, presence of this translocation may have some prognostic value.
大多数骨髓增生异常综合征(MDS)表现为染色体物质的丢失或增加,较少见的情况是仅以易位作为唯一异常表现。此外,某些易位在MDS中比其他易位更常见,但据我们所知,t(6;15)在MDS中尚未见报道,尤其是治疗相关的MDS(t-MDS)病例。t-MDS患者是一组因细胞毒性和/或放射治疗的潜在并发症而导致的异质性干细胞相关疾病,总体预后通常比原发性MDS更差。我们报告了一例独特的患者,该患者最初表现为急性髓系白血病(AML),核型正常,伴有FLT3-ITD和NPM1突变。患者接受化疗和自体骨髓移植治疗成功,但在移植三年后出现了一种新的FLT3-ITD阴性的t-MDS,并伴有一种独特的易位,即t(6;15)(q12;q15)。据我们所知,这种独特的单一易位在MDS或t-MDS中从未有过报道,鉴于她对治疗的成功反应和缓解情况,这种易位的存在可能具有一定的预后价值。