Perrot J L, Lanthier K, Benoit F, Graille M C, Guy C, Bertheas M F, Cambazard F
Service de Dermatologie, CHU Saint-Etienne.
Ann Dermatol Venereol. 1995;122(10):663-6.
Secondary myelodysplasia after antimitotic therapy is a rare complication usually observed with alkylating agents. The condition usually progresses to acute leukaemia with very poor short term prognosis.
We report the cases of 2 women who developed myelodysplasia 2 and 9 months after treatment associating dacarbazine and fotemustine for visceral metastases of a malignant melanoma.
The frequency of these rare complications is probably underestimated because of the rapid unfavourable outcome of metastatic malignant melanoma. We were unable to determine whether dacarbazine, fotemustine or their combination was incriminated in this complication. Risk could be reduced by carefully determining the cumulative doses of these antimitotics.
抗有丝分裂治疗后发生的继发性骨髓发育异常是一种罕见的并发症,通常见于烷化剂治疗后。这种情况通常会进展为急性白血病,短期预后很差。
我们报告了2例女性患者的病例,她们在使用达卡巴嗪和福莫司汀联合治疗恶性黑色素瘤内脏转移后2个月和9个月出现了骨髓发育异常。
由于转移性恶性黑色素瘤的不良结局迅速,这些罕见并发症的发生率可能被低估了。我们无法确定达卡巴嗪、福莫司汀或它们的联合使用是否与这种并发症有关。通过仔细确定这些抗有丝分裂药物的累积剂量,可以降低风险。