Abla Oussama, Gassas Adam, Stevens Robert, Grant Ronald, Abdelhaleem Mohamed
The Hospital for Sick Children, Toronto, Ontario, Canada.
J Pediatr Hematol Oncol. 2006 Feb;28(2):98-9. doi: 10.1097/01.mph.0000199589.21797.dd.
The authors report an unusual presentation of a Philadelphia chromosome-positive acute lymphoblastic leukemia with two unusual features: a bcr-abl fusion mRNA coding for p210 protein and a T-cell immunophenotype. The patient was a 16-year-old boy who presented with septic shock and pancytopenia, likely precipitated by an acute parvovirus B19 infection. Management consisted of supportive therapy, followed by chemotherapy for T-cell acute lymphoblastic leukemia and stem cell transplantation. He died 8 months after transplant due to idiopathic pneumonia syndrome, but without evidence of relapsed disease.
编码p210蛋白的bcr-abl融合mRNA和T细胞免疫表型。患者为一名16岁男孩,表现为感染性休克和全血细胞减少,可能由急性B19细小病毒感染引发。治疗包括支持性治疗,随后进行T细胞急性淋巴细胞白血病化疗和干细胞移植。他在移植后8个月因特发性肺炎综合征死亡,但无疾病复发证据。