Congenital Acute Myeloid Leukemia with Unique Translocation t(11;19)(q23;p13.3)

被引:1
|
作者
Yarbrough, Chester K. [1 ]
Bandt, S. Kathleen [2 ]
Hurth, Kyle [3 ]
Wambach, Jennifer A. [4 ]
Rao, Rakesh [4 ]
Kulkarni, Shashikant [5 ]
White, Francis V. [5 ]
Frater, John L. [5 ]
Leonard, Jeffrey R. [6 ]
机构
[1] Washington Univ, Sch Med, St Louis, MO 63130 USA
[2] Washington Univ, Sch Med, Neurol Surg, St Louis, MO USA
[3] USC, Keck Sch Med, Pathol, Neuropathol, Los Angeles, CA USA
[4] Washington Univ, Sch Med, Newborn Med, Pediat, St Louis, MO USA
[5] Washington Univ, Sch Med, Pathol & Immunol, St Louis, MO USA
[6] Ohio State Univ, Nationwide Childrens Hosp, Neurol Surg, Columbus, OH 43210 USA
来源
CUREUS | 2015年 / 7卷 / 07期
关键词
congenital leukemia; fetal leukemia; subdural hematoma; 11q23; mll rearrangement; 19p13.3;
D O I
10.7759/cureus.289
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Congenital leukemia is rarely encountered in clinical practice, even in tertiary children's hospitals. Leukemia may cause significant coagulopathy, putting the patient at risk of intracranial hemorrhage. In this case, the authors present a female infant with a unique mixed phenotypic congenital acute myeloid leukemia showing mixed-lineage leukemia (MLL) rearrangement and severe coagulopathy resulting in a large subdural hematoma. Despite the fatal outcome in this case, neurosurgical treatment of patients with acute myeloid leukemia should be considered if coagulopathy and the clinical scenario allow.
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页数:8
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