Tsujimoto Hiroshi, Kounami Shinji, Mitani Yasuyuki, Watanabe Takashi, Takifuji Katsunari
Department of Pediatrics, Wakayama Medical University, 811-1 Kimiidera, Wakayama, Japan.
Department of Second Surgery, Wakayama Medical University, 811-1 Kimiidera, Wakayama, Japan.
Case Rep Hematol. 2015;2015:610581. doi: 10.1155/2015/610581. Epub 2015 Jul 1.
Neonatal acute megakaryoblastic leukemia (AMKL) without Down syndrome (DS) is an extremely rare disorder. We report of a one-day-old male infant without DS who developed AMKL with leukemia cutis and right facial nerve palsy. Magnetic resonance imaging of the patient's brain revealed multiple intracranial tumors. A biopsy specimen of the skin lesion was suggestive of AMKL, but the bone marrow leukemic cells were less than 5% of the marrow nucleated cells. The skin and intracranial lesions had spontaneously regressed within one and a half months, but the patient's anemia and thrombocytopenia gradually worsened and the leukemic cells in the bone marrow gradually increased to more than 20% of the nucleated cells. In addition, multiple intracranial lesions reappeared at 72 days of life. We diagnosed the patient with AMKL, and chemotherapy followed by unrelated cord blood transplantation after a reduced-intensity conditioning regimen resulted in sustained complete remission. At present, the patient is well, and he has demonstrated normal development for five years.
非唐氏综合征(DS)的新生儿急性巨核细胞白血病(AMKL)是一种极其罕见的疾病。我们报告了一名无DS的1日龄男婴,其患AMKL并伴有皮肤白血病和右侧面神经麻痹。该患者脑部的磁共振成像显示有多个颅内肿瘤。皮肤病变的活检标本提示为AMKL,但骨髓白血病细胞少于骨髓有核细胞的5%。皮肤和颅内病变在一个半月内自发消退,但患者的贫血和血小板减少逐渐加重,骨髓中的白血病细胞逐渐增加至有核细胞的20%以上。此外,在出生72天时多个颅内病变再次出现。我们诊断该患者患有AMKL,化疗后采用减低强度预处理方案进行非亲缘脐带血移植,结果实现了持续完全缓解。目前,患者情况良好,且已表现出五年的正常发育。