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Successful outcome of Langerhans cell histiocytosis complicated by therapy-related myelodysplasia and acute myeloid leukemia: a case report

机译:朗格汉斯细胞组织细胞增生症并发与治疗有关的骨髓增生异常和急性髓性白血病的成功结果:一例报告

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Background Various therapeutic options are available for the management of Langerhans cell histiocytosis. However, treatment administered to control this disease may be complicated by acute leukemia. Case presentation A 34 years old male was diagnosed to have Langerhans cell histiocytosis in March 1999. Unfortunately, the cytotoxic chemotherapy and radiotherapy given to control the repeated relapses and exacerbations of the primary disease predisposed him to therapy-induced myelodysplastic syndrome which transformed into acute myeloid leukemia. After achieving complete remission of his leukemia, the patient received an allogeneic hematopoietic stem cell transplant. The allograft was complicated by chronic graft versus host disease that was controlled by various immunosuppressive agents and extracorporal photophoresis. Conclusion Management of complicated cases of histiocytosis requires various therapeutic modalities and a multidisciplinary approach. Having complications of therapy eg myelodysplasia or acute leukemia make the outcome more dismal and the management options limited to aggressive forms of treatment. High dose chemotherapy followed by an allograft may be a curative option not only for therapy-related myelodysplasia/acute leukemia, but also for frequently relapsing and poorly controlled Langerhans cell histiocytosis.
机译:背景技术各种治疗选择可用于朗格汉斯细胞组织细胞增生症的管理。但是,为控制这种疾病而进行的治疗可能会并发急性白血病。病例报告1999年3月,一名34岁的男性被诊断患有朗格汉斯细胞组织细胞增生症。不幸的是,为控制原发性疾病的反复发作和恶化而进行的细胞毒性化学疗法和放射疗法使他易感于由治疗引起的骨髓增生异常综合症,该综合症转化为急性髓样白血病。白血病完全缓解后,患者接受了异基因造血干细胞移植。慢性移植物抗宿主病使同种异体移植物变得复杂,该疾病由各种免疫抑制剂和体外电泳控制。结论处理组织细胞增多症的复杂病例需要多种治疗方法和多学科方法。具有治疗并发症,例如骨髓增生异常或急性白血病会使结果更加令人沮丧,并且治疗选择仅限于积极的治疗形式。高剂量化疗后同种异体移植可能不仅是治疗相关的骨髓增生异常/急性白血病的治疗方法,而且对于频繁复发且控制不良的朗格汉斯细胞组织细胞增生症可能是一种治疗选择。

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