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作 者:侯军[1] 胡晓静[1] 韩颖[1] 孟秀琴[1] 施菊妹[1]
机构地区:[1]同济大学附属第十人民医院血液科,上海200072
出 处:《临床血液学杂志》2014年第1期66-68,共3页Journal of Clinical Hematology
基 金:上海市卫生局资助项目(No:2010081)
摘 要:1病例资料患者,男,56岁,既往体健,无神经系统疾病史。2012年11月起无明显诱因突发左侧肢体麻木、无力,伴前胸部节段性紧绷感、麻木感,且症状进行性加重,并出现右侧肢体和足底麻木,伴腹胀、嗳气,无口角流涎,无头晕、头痛、胸闷、胸痛、腹痛、呕血及黑便。有盗汗,半年体重下降10kg。A case of 56years old male mantle cell lymphoma(MCL)patient with central nervous system in- filtration as the initial symptom was reported.He had a progressive limbs numbness and weakness firstly and then appeared chest segmental tension.Electromyography showed the neurogenic damage in double arms.Cerebrospinal fluid infiltration was confirmed by a large number of white blood cells(10.0×106/L)and high concentration of protein(1 007mg/L).Flow cytometry analysis of cerebrospinal fluid revealed 6.7percent of abnormal cells,posi- tive for CD5and negative for CD10expression at the same time.PET-CT demonstrated that there had a mild in- creased intake of FDG in cervical and thoracic spine without obvious destruction in vertebral body.Routine blood test showed that the number of white blood cells was 21.89×10^9/L with 31percent of abnormal cells.Further- more,the laboratory results showed 5percent of blast lymphocytic cells in bone marrow and 38.3percent of mono- clonal mature small B lymphocytic cells with CD5-positive and CD10-negative expression in peripheral blood.FISH showed IGH/CCND1(+)fusion gene.At last,this patient was diagnosed with MCL.
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