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与阿苯达唑诱发全血细胞减少相关的死亡:病例报告及文献复习

Death related to albendazole-induced pancytopenia: case report and review.

作者信息

Opatrny Lucie, Prichard Roger, Snell Linda, Maclean J Dick

机构信息

Division of Clinical Epidemiology, Royal Victoria Hospital, McGill University Hospital Center, Montreal, Quebec, Canada.

出版信息

Am J Trop Med Hyg. 2005 Mar;72(3):291-4.

Abstract

Albendazole is a benzimidazole with wide spectrum coverage as an antiparasitic drug. Reported side effects have been minimal. We report the case of a patient who died with severe prolonged pancytopenia beginning during the third week of therapy for a pulmonary echinococcal cyst. This case was a 68-year-old man who presented with a large cystic lung mass. His medical history was significant for Child-Pugh class B cirrhosis. A prolonged course of albendazole was initiated. Two weeks later, the patient presented in septic shock with severe pancytopenia. The patient was initially resuscitated, but died after 10 days with no marrow recovery. Autopsy was consistent with albendazole-induced pancytopenia. This is the third human case of pancytopenia and the first death reported in relation to albendazole-induced pancytopenia. Neutropenia seems to be related more to higher dosage and longer duration of use. Albendazole sulfoxide peak dose and half life are significantly prolonged by liver disease and concomitant administration of certain drugs. The severity and duration of albendazole-induced pancytopenia in this case was likely related to the underlying liver disease. Frequent serial monitoring of blood counts and cessation of medication with any evidence of marrow toxicity in such patients is warranted.

摘要

阿苯达唑是一种具有广泛抗寄生虫谱的苯并咪唑类药物。报告的副作用极少。我们报告了一例患者,该患者在治疗肺棘球蚴囊肿的第三周开始出现严重的长期全血细胞减少症并死亡。该病例为一名68岁男性,表现为肺部巨大囊性肿块。他有Child-Pugh B级肝硬化病史。开始了长时间的阿苯达唑治疗。两周后,患者出现感染性休克并伴有严重全血细胞减少症。患者最初经复苏,但10天后死亡,骨髓未恢复。尸检结果与阿苯达唑引起的全血细胞减少症相符。这是第三例人类全血细胞减少症病例,也是首例与阿苯达唑引起的全血细胞减少症相关的死亡报告。中性粒细胞减少似乎与较高剂量和较长使用时间关系更大。肝病和同时使用某些药物会显著延长阿苯达唑亚砜的峰值剂量和半衰期。该病例中阿苯达唑引起的全血细胞减少症的严重程度和持续时间可能与潜在的肝病有关。对于此类患者,有必要频繁进行连续血常规监测,并在出现任何骨髓毒性迹象时停药。

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