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[米托蒽醌相关的多发性硬化症急性白血病。不明原因血细胞减少的病例报告及实用方法]

[Mitoxantrone-related acute leukemia by multiple sclerosis. Case report and practical approach by unclear cytopenia].

作者信息

Meyer C, Ansorge N, Siglienti I, Salmen S, Stroet A, Nückel H, Dührsen U, Ritter P R, Schmidt W E, Gold R, Chan A

机构信息

Neurologische Klinik, St.-Josef-Hospital, Klinikum der Ruhr-Universität Bochum, Gudrunstraße 56, 44791, Bochum.

出版信息

Nervenarzt. 2010 Dec;81(12):1483-9. doi: 10.1007/s00115-010-3041-5.

Abstract

BACKGROUND

Mitoxantrone is highly efficacious in the treatment of severe multiple sclerosis (MS). Mitoxantrone therapy-related acute leukemia (TRAL) has recently become the focus of interest.

METHODS

A case report of fatal TRAL following mitoxantrone therapy is presented with a discussion on the differential diagnosis and risk factors. The interdisciplinary development of diagnostic and therapeutic algorithms is presented from a haematological and neurological point of view.

RESULTS

We describe the case of a 34-year-old MS patient who developed TRAL following mitoxantrone therapy (cumulative dose 45 mg/m(2) body surface). The patient died from endocarditis. TRAL is a rare but potentially fatal complication of mitoxantrone therapy with a wide variation of reported incidence. Thus far, no specific risk factors relating for example to preceding therapy and treatment regimens have been identified. Frequent laboratory controls and early bone marrow aspiration are mandatory for suspected TRAL as the condition is potentially curable.

CONCLUSIONS

TRAL needs to be considered in the risk-benefit assessment of mitoxantrone therapy, however, the exact incidence and risk factors (e.g. dosage, treatment regimen) are still unclear. The risks are controllable under close surveillance and early diagnosis is important for prognosis. Future investigations need to concentrate on identification of potential risk factors.

摘要

背景

米托蒽醌在治疗严重多发性硬化症(MS)方面疗效显著。米托蒽醌治疗相关急性白血病(TRAL)最近成为关注焦点。

方法

本文报告了1例米托蒽醌治疗后发生致命性TRAL的病例,并对鉴别诊断和危险因素进行了讨论。从血液学和神经学角度介绍了诊断和治疗算法的跨学科发展情况。

结果

我们描述了1例34岁的MS患者,其在接受米托蒽醌治疗(累积剂量45mg/m²体表面积)后发生TRAL。该患者死于心内膜炎。TRAL是米托蒽醌治疗一种罕见但可能致命的并发症,报道的发病率差异很大。迄今为止,尚未确定例如与先前治疗和治疗方案相关的具体危险因素。对于疑似TRAL,必须进行频繁的实验室检查和早期骨髓穿刺,因为该病症有可能治愈。

结论

在米托蒽醌治疗的风险效益评估中需要考虑TRAL,然而,确切的发病率和危险因素(如剂量、治疗方案)仍不清楚。在密切监测下风险是可控的,早期诊断对预后很重要。未来的研究需要集中于识别潜在危险因素。

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