Successful treatment of cutaneous leishmaniasis with lipid formulations of amphotericin B in two immunocompromised patients

被引:52
作者
Amato, VS
Rabello, A
Rotondo-Silva, A
Kono, A
Maldonado, TPH
Alves, IC
Floeter-Winter, LM
Neto, VA
Shikanai-Yasuda, MA
机构
[1] Univ Sao Paulo, Fac Med, Hosp Clin, Infect & Parasit Dis Clin, BR-05403010 Sao Paulo, Brazil
[2] Fiocruz MS, Fundacao Oswaldo Cruz, Ctr Pesquisas Rene Rachou, Lab Clin Res, BR-30190002 Belo Horizonte, MG, Brazil
[3] Univ Sao Paulo, Fac Med, Hosp Clin, Lab Immunol LIM 48, BR-05403000 Sao Paulo, Brazil
[4] Univ Sao Paulo, Inst Biomed, Dept Parasitol, Mol Biol Leishmania, BR-05508900 Sao Paulo, Brazil
[5] Univ Sao Paulo, Fac Med, Hosp Clin, Lab Med Invest Parasitol LIM46, BR-05403000 Sao Paulo, Brazil
[6] Univ Sao Paulo, Fac Med, Hosp Clin, Lab Immunol LIM 48, BR-05403010 Sao Paulo, Brazil
[7] Univ Sao Paulo, Fac Med, Dept Infect & Parasit Dis, BR-05403010 Sao Paulo, Brazil
关键词
cutaneous leishmaniasis; American tegumentary leishmaniasis; lipid formulations of amphotericin B; leishmaniasis; human immunodeficiency virus;
D O I
10.1016/j.actatropica.2004.06.006
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Pentavalent antimonial drugs are habitually the first choice for treating leishmaniasis, although they possess well-known toxicity and may present some therapeutic failure. Lipid formulations of amphotericin B (LFAB) have been increasingly used for treating several types of leishmaniasis. However, the administration of such lipid formulations specifically to patients with cutaneous leishmaniasis (CL) is still rare, including immunocompromised patients to whom standard treatments are more frequently contraindicated. We describe here two cases of immunocompromised patients with CL, one of them with AIDS, representing the first case of AIDS and CL co-infection treated with LFAB described in the literature. The patient achieved therapeutic success with a total 1.500 mg dose of amphotericin B colloidal dispersion. The other had diabetes mellitus as well as kidney failure and was under dialysis, having obtained the healing of lesion with a total dose of 600 mg of liposomal amphotericin B. Thus, the authors suggest that LFAB can represent a safe, efficient and less toxic therapeutic alternative to pentavalent antimonials, as well as to the so-called second line drugs, pentamidine and amphotericin B deoxycholate. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 132
页数:6
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