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Subdural hematomas in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia receiving imatinib mesylate in conjunction with systemic and intrathecal chemotherapy.

机译:接受甲磺酸伊马替尼联合全身和鞘内化疗的费城染色体阳性急性淋巴细胞白血病患者的硬膜下血肿。

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Imatinib mesylate and other tyrosine kinase inhibitors (TKIs) that inhibit BCR-ABL have had a favorable impact on the treatment of Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL). TKIs are generally well tolerated, but they can induce platelet dysfunction, which is of particular concern in the setting of thrombocytopenia in patients with acute leukemia. We present three patients with Ph+ ALL receiving imatinib mesylate in conjunction with systemic and intrathecal chemotherapy who developed subdural hematomas (SDHs). All three were thrombocytopenic and had undergone repeated lumbar punctures for prophylactic intrathecal chemotherapy, but they were not coagulopathic and did not have meningeal leukemia. SDHs occurred in three of a total of 10 adult patients with Ph+ ALL receiving imatinib mesylate in conjunction with systemic and intrathecal chemotherapy at our institution from 2007 to 2010, but in none of 22 adult patients with Ph- ALL receiving the same therapy without imatinib mesylate (p < 0.05). Patients with Ph+ ALL receiving imatinib mesylate, and likely also dasatinib, in conjunction with systemic and intrathecal chemotherapy may be at increased risk of SDH, and should be closely monitored for subtle manifestations of this complication.
机译:甲磺酸伊马替尼和其他抑制BCR-ABL的酪氨酸激酶抑制剂(TKIs)对费城染色体阳性(Ph +)急性淋巴细胞白血病(ALL)的治疗产生了有利影响。 TKI通常具有良好的耐受性,但它们可诱发血小板功能障碍,这在急性白血病患者的血小板减少症的发生中尤其令人关注。我们介绍了三名Ph + ALL患者,他们接受了甲磺酸伊马替尼联合全身和鞘内化疗,并发展了硬膜下血肿(SDHs)。所有这三个都是血小板减少性的,并且已经进行了反复的腰椎穿刺以进行预防性鞘内化疗,但是它们不是凝结性的,也没有脑膜白血病。从2007年到2010年,在我们机构的10名接受甲磺酸伊马替尼联合全身和鞘内化疗的成年Ph + ALL成人患者中,有3例发生了SDH,但22例接受相同甲磺酸伊马替尼治疗的成年Ph-ALL患者中均没有发生SDH (p <0.05)。接受甲磺酸伊马替尼治疗的Ph + ALL患者,可能还有达沙替尼,以及全身和鞘内化疗,均可能增加SDH的风险,应密切监测这种并发症的微妙表现。

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