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克氏锥虫病再激活:两名免疫抑制患者的皮肤表现。

Reactivation of Chagas' disease: cutaneous manifestations in two immunosuppressed patients.

机构信息

Department of Dermatology, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.

出版信息

Int J Dermatol. 2012 Jul;51(7):829-34. doi: 10.1111/j.1365-4632.2011.05224.x.

Abstract

BACKGROUND

Chagas' disease is a zoonosis caused by a protozoan agent, Trypanosoma cruzi. Patients undergoing immunosuppressive treatment due to organ transplant, malignancies, infections, or chemotherapy may reactivate a preexisting chronic or indeterminate Trypanosoma cruzi infection.

METHODS

We present two transplant patients who underwent reactivation of Chagas' disease with cutaneous manifestations after an augmentation in their immunosuppressive therapy. A 38-year-old man was hospitalized on day 69 after receiving an allogeneic bone marrow transplant; he developed multiple painful erythematous plaques with diffuse borders, confined to the right cheek, trunk, thigh, elbows, and feet. A 59-year-old woman with a 14-year history of Chagasic cardiomyopathy presented one month after heart transplantation with a painful infiltrated purpuric plaque on the back of her right leg.

RESULTS

In both cases, histologic examination of skin biopsies showed dermal infiltration with intrahistiocytic amastigotes. In one of the reported cases, the Strout method detected parasitemia. Treatments with nifurtimox (600 mg/d) in case 1 and benznidazole (400 mg/d) in case 2 were started. Fever and cutaneous lesions resolved immediately after seven days of treatment.

CONCLUSIONS

Reactivation of Chagas' disease is a serious complication that usually occurs in immunocompromised patients. Clinical manifestations include febrile illness occasionally associated with painful skin lesions. Early diagnosis and proper treatment can significantly improve these patients' outcome.

摘要

背景

恰加斯病是一种由原生动物寄生虫克氏锥虫引起的动物源性疾病。由于器官移植、恶性肿瘤、感染或化疗而接受免疫抑制治疗的患者可能会使先前存在的慢性或不确定的克氏锥虫感染重新激活。

方法

我们报告了两名移植患者,他们在免疫抑制治疗增强后出现了伴有皮肤表现的恰加斯病再激活。一名 38 岁男性在接受异基因骨髓移植后第 69 天住院,他出现了多个疼痛性红斑性斑块,边界弥漫,局限于右脸颊、躯干、大腿、肘部和脚部。一名 59 岁女性患有 14 年恰加斯心肌病史,在心脏移植后 1 个月出现右小腿后侧疼痛性浸润性紫癜斑块。

结果

在这两种情况下,皮肤活检的组织学检查均显示真皮内有组织内阿米巴内寄生体浸润。在报告的病例中,Strout 方法检测到寄生虫血症。在第 1 例中开始使用硝呋莫司(600 mg/d)治疗,在第 2 例中开始使用苯硝唑(400 mg/d)治疗。在开始治疗的 7 天后,发热和皮肤病变立即得到缓解。

结论

恰加斯病再激活是一种严重的并发症,通常发生在免疫功能低下的患者中。临床表现包括发热性疾病,偶尔伴有疼痛性皮肤病变。早期诊断和适当的治疗可以显著改善这些患者的预后。

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