患有 21 三体综合征、一过性骨髓造血异常和神经纤维瘤病 1 型的新生儿嗜酸性粒细胞增多症

IF 0.9 4区 医学 Q4 HEMATOLOGY Journal of Pediatric Hematology/Oncology Pub Date : 2024-11-01 Epub Date: 2024-09-18 DOI:10.1097/MPH.0000000000002950
Kayla M Schmittau, Brian M Walker, Nupur Mittal, Lisa Giordano
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引用次数: 0

摘要

一过性骨髓造血异常是一种导致未成熟髓系细胞过度增殖的综合征,在患有 21 三体综合征的新生儿中,10%-15% 会出现这种情况。一过性骨髓造血异常通常可自行缓解,但偶尔也需要化疗。这种疾病通常不伴有嗜酸性粒细胞增多。我们报告了一名患有 21 三体综合征并以白细胞增多和明显嗜酸性粒细胞增多为特征的一过性骨髓造血异常的新生儿。患者需要使用两个周期的阿糖胞苷才能充分控制骨髓增生。此外,这名患者后来还被诊断出患有神经纤维瘤病 1 型,而该病与 21 三体综合征或一过性骨髓增生异常并无关联。
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Eosinophilia in a Neonate With Trisomy 21, Transient Abnormal Myelopoiesis, and Neurofibromatosis Type 1.

Transient abnormal myelopoiesis is a syndrome that causes excess proliferation of immature myeloid cells and occurs in 10% to 15% of neonates with trisomy 21. Transient abnormal myelopoiesis usually resolves spontaneously but occasionally requires treatment with chemotherapy. The disorder is not typically associated with eosinophilia. We report on a neonate with trisomy 21 and transient abnormal myelopoiesis characterized by leukocytosis with marked eosinophilia. The patient required 2 cycles of cytarabine for adequate myeloproliferative control. Furthermore, this patient was subsequently also diagnosed with neurofibromatosis type 1, which has no known association with trisomy 21 or transient abnormal myelopoiesis.

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来源期刊
CiteScore
1.90
自引率
8.30%
发文量
415
审稿时长
2.5 months
期刊介绍: ​Journal of Pediatric Hematology/Oncology (JPHO) reports on major advances in the diagnosis and treatment of cancer and blood diseases in children. The journal publishes original research, commentaries, historical insights, and clinical and laboratory observations.
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