Liver disease is frequently observed in Down syndrome patients with transient abnormal myelopoiesis

被引:0
作者
Myoung Ja Park
Manabu Sotomatsu
Kentaro Ohki
Kokoro Arai
Kenichi Maruyama
Tomio Kobayashi
Akira Nishi
Kiyoko Sameshima
Takeshi Takagi
Yasuhide Hayashi
机构
[1] Gunma Children’s Medical Center,Department of Hematology/Oncology
[2] Gunma Children’s Medical Center,Department of Neonatology
[3] Gunma Children’s Medical Center,Department of Cardiology
[4] Gunma Children’s Medical Center,Department of Pediatric Surgery
[5] Gunma Children’s Medical Center,Department of Genetics
[6] Gunma Children’s Medical Center,Department of Obstetrics
来源
International Journal of Hematology | 2014年 / 99卷
关键词
Down syndrome; AML; Liver disease; Direct bilirubin; Cytarabine therapy;
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学科分类号
摘要
Transient abnormal myelopoiesis (TAM) in neonates with Down syndrome (DS) is characterized by the transient appearance of blast cells, which resolves spontaneously. Approximately 20 % of patients with TAM die at an early age due to organ failure, including liver disease. We studied 25 DS-TAM patients retrospectively to clarify the correlation between clinical and laboratory characteristics and liver diseases. Early death (<6 months of age) occurred in four of the 25 patients (16.0 %), and two of those four patients died due to liver failure. Although physiologic jaundice improved gradually after a week, all DS patients had elevated D-Bil levels during the clinical course of TAM, except one who suffered early death. The median peak day of the WBC count, total bilirubin (T-Bil) and D-Bil levels was: day 1 (range day 0–57), day 8 (range day 1–55), and day 17 (range 1–53), respectively. Our results reveal that all patients with DS-TAM may develop liver disease irrespective of the absence or presence of symptoms and risk factors for early death. In patients of DS-TAM, careful observation of the level of D-Bil is needed by at least 1 month of age for the detection of liver disease risk.
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页码:154 / 161
页数:7
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