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新生儿急性巨核细胞白血病伴皮肤白血病和多发颅内病变,通过无关脐血移植成功治疗

Neonatal Acute Megakaryoblastic Leukemia Presenting with Leukemia Cutis and Multiple Intracranial Lesions Successfully Treated with Unrelated Cord Blood Transplantation.

作者信息

Tsujimoto Hiroshi, Kounami Shinji, Mitani Yasuyuki, Watanabe Takashi, Takifuji Katsunari

机构信息

Department of Pediatrics, Wakayama Medical University, 811-1 Kimiidera, Wakayama, Japan.

Department of Second Surgery, Wakayama Medical University, 811-1 Kimiidera, Wakayama, Japan.

出版信息

Case Rep Hematol. 2015;2015:610581. doi: 10.1155/2015/610581. Epub 2015 Jul 1.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c7e/4502332/5cd89a1c833c/CRIHEM2015-610581.001.jpg

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