Dictar M, Sinagra A, Verón M T, Luna C, Dengra C, De Rissio A, Bayo R, Ceraso D, Segura E, Koziner B, Riarte A
Bone Marrow Transplant Unit and Infectious Diseases Service, CP Independencia, Buenos Aires, Capital Federal, Argentina.
Bone Marrow Transplant. 1998 Feb;21(4):391-3. doi: 10.1038/sj.bmt.1701107.
We report the clinical course of five adult patients with chronic Chagas' disease (Cd) who underwent BMT. Two patients with non-Hodgkin's lymphoma and one with ALL received an ABMT. Allogeneic BMT was performed in two patients with AML and CML respectively. One donor had chronic Cd. Samples of peripheral blood for parasite investigation by the Strout method, blood culture, and immunological studies by indirect immunofluorescent assay, ELISA and indirect hemagglutination tests were performed weekly from the start of chemotherapy until day +60 for ABMT and during the period of immunosuppression for allogeneic BMT. No prophylaxis was given to any of these patients. In only one ABMT patient were trypomastigotes detected early by blood culture without symptoms of reactivation. Benznidazole as preemptive treatment was administered at 5-8 mg/kg/daily for 30 days. Parasitemia was rapidly cleared and at the end of therapy xenodiagnosis was negative. The other Cd patients showed no evidence of relapse of parasitemia or signs and symptoms of reactivation. In brief, evidence of Cd should be sought in all BMT patients coming from endemic areas because parasitemia and reactivation are potential complications during the period of neutropenia and immunosuppression. The strategy used for early detection and treatment of parasitemia and reactivation was safe and effective.
我们报告了5例接受骨髓移植(BMT)的成年慢性恰加斯病(Cd)患者的临床病程。2例非霍奇金淋巴瘤患者和1例急性淋巴细胞白血病患者接受了自体骨髓移植(ABMT)。2例急性髓系白血病(AML)和慢性髓系白血病(CML)患者分别接受了异基因BMT。1名供者患有慢性Cd。从化疗开始至ABMT的第+60天以及异基因BMT的免疫抑制期间,每周进行外周血样本检测,采用Strout方法进行寄生虫检查、血培养,并通过间接免疫荧光测定、酶联免疫吸附测定(ELISA)和间接血凝试验进行免疫学研究。这些患者均未接受预防性治疗。仅1例ABMT患者通过血培养早期检测到锥鞭毛体,但无再激活症状。给予苯硝唑进行抢先治疗,剂量为5 - 8mg/kg/天,持续30天。寄生虫血症迅速清除,治疗结束时虫媒接种诊断为阴性。其他Cd患者未出现寄生虫血症复发或再激活的体征和症状。简而言之,对于所有来自流行地区的BMT患者,均应寻找Cd证据,因为在中性粒细胞减少和免疫抑制期间,寄生虫血症和再激活是潜在的并发症。用于早期检测和治疗寄生虫血症及再激活的策略是安全有效的。