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全反式维甲酸治疗青年急性早幼粒细胞白血病致多发颅神经病变和颅内高压

Multiple cranial neuropathy and intracranial hypertension associated with all-trans retinoic acid treatment in a young adult patient with acute promyelocytic leukemia.

机构信息

Servicio de Hematología, Hospital Universitario de Salamanca, Paseo de San Vicente, 58-182, Salamanca 37007, Spain.

出版信息

Int J Hematol. 2012 Sep;96(3):383-5. doi: 10.1007/s12185-012-1134-6. Epub 2012 Jul 6.

Abstract

All-trans retinoic acid (ATRA) induces complete remission in 64-100 % of patients with acute promyelocytic leukemia (APL), and is considered to be a safe agent. Pseudotumor cerebri is a neurological side effect of ATRA reported in pediatric patients, and which is characterized by raised cerebrospinal fluid pressure in the absence of any intracranial pathology or secondary causes of intracranial hypertension. Involvement of cranial nerves other than II and VI is very uncommon in idiopathic intracranial hypertension (IIH); peripheral facial nerve palsy is exceptional and has rarely been described in the context of treatment with ATRA. We describe the case of a 15-year-old female patient with APL who developed an IIH and involvement of cranial nerves (bilateral papilledema, left facial and right sixth nerves) after receiving induction therapy including ATRA. Viral infections and other causes of secondary cranial nerve lesions were excluded. Symptoms completely subsided with the temporary withdrawal of ATRA and did not recur after reintroducing the drug. To date, the patient has managed to receive the treatment as per protocol. In conclusion, we report an atypical presentation of IIH that merits consideration, especially with respect to young patients with APL receiving ATRA; our most important observation is that the drug could be safely reintroduced once the symptoms had resolved.

摘要

全反式维甲酸(ATRA)可诱导 64%-100%的急性早幼粒细胞白血病(APL)患者完全缓解,被认为是一种安全的药物。假性脑瘤是 ATRA 在儿科患者中报告的一种神经系统副作用,其特征是在没有任何颅内病理或颅内压升高的继发原因的情况下,脑脊液压力升高。在特发性颅内高压(IIH)中,除第二和第六脑神经外,其他脑神经受累非常罕见;特发性颅内高压中很少描述外周面神经麻痹,在接受 ATRA 治疗的情况下更是如此。我们描述了一例 15 岁女性 APL 患者的病例,该患者在接受包括 ATRA 在内的诱导治疗后,出现 IIH 和脑神经受累(双侧视盘水肿、左侧面神经和右侧第六脑神经)。排除了病毒感染和其他引起继发性脑神经病变的原因。症状在暂时停用 ATRA 后完全缓解,重新引入药物后未再复发。迄今为止,该患者已按方案接受了治疗。总之,我们报告了一种需要考虑的 IIH 不典型表现,尤其是在接受 ATRA 治疗的 APL 年轻患者中;我们最重要的观察是,一旦症状缓解,药物可以安全重新引入。

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