伊马替尼诱导的儿童慢性髓性白血病腹膜后纤维化:1例报告。

American journal of blood research Pub Date : 2021-12-15 eCollection Date: 2021-01-01
Swaminathan Keerthivasagam, Nirmalya Roy Moulik, Ankita Pandey, Kunal Gala, Vasundhara Patil, Chetan Dhamne, Gaurav Chatterjee, Nikhil Patkar, Gaurav Narula, Shripad Banavali
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引用次数: 0

摘要

一名患有慢性髓性白血病(CML)的12岁男孩在接受伊马替尼治疗约41个月后表现为双侧凹陷性足水肿和腹胀,根据影像学和活检结果诊断为腹膜后纤维化(RPF)。他被发现有双侧输尿管积水,需要双j型支架置入影响更严重的右输尿管。伊马替尼被短暂中断,后来由于转录水平上升和当时无法获得其他替代品,后来被达沙替尼取代,一旦通用版本可用。患儿在植入DJ支架18个月后仍无症状。RPF是伊马替尼的罕见并发症,这是文献中报道的第二例。
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Imatinib-induced retroperitoneal fibrosis in a child with chronic myeloid leukemia: a case report.

A 12 year old boy with chronic myeloid leukemia (CML) presenting with bilateral pitting pedal edema and abdominal distension after about 41 months of imatinib therapy and was diagnosed to have retroperitoneal fibrosis (RPF) based on imaging and biopsy findings. He was found to have bilateral hydroureteronephrosis needing double-J stenting to the more severely affected right ureter. Imatinib was briefly interrupted and restarted later due to rising transcript levels and unavailability of other alternatives at that time which was later substituted by dasatinib once generic versions became available. Child remains asymptomatic after 18 months of DJ stenting. RPF is a rare complication of imatinib this being the second case reported in the literature.

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来源期刊
American journal of blood research
American journal of blood research MEDICINE, RESEARCH & EXPERIMENTAL-
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