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内脏利什曼病:肝移植后诊断困难的病例报告。

Visceral Leishmaniasis: A Case Report of a Challenging Diagnosis After Orthotopic Liver Transplantation.

机构信息

Liver Transplant Division, Real Hospital Português, Recife, Brazil.

Liver Transplant Division, Real Hospital Português, Recife, Brazil.

出版信息

Transplant Proc. 2022 Jul-Aug;54(6):1657-1660. doi: 10.1016/j.transproceed.2022.05.008. Epub 2022 Jul 4.

Abstract

Leishmaniasis is a disease caused by a protozoan and transmitted by sandfly species in several emerging countries. Visceral leishmaniasis is a serious complication, especially in immunosuppressed patients, and is uncommon after liver transplantation. We report the case of a 48-year-old female patient who underwent liver transplantation owing to polycystic liver disease. Six months after the procedure, she was hospitalized with diarrhea, acute kidney failure, and leukopenia. She had been off steroids for 3 months and was taking mycophenolate and tacrolimus. She had already been treated for cytomegalovirus, which was negative on admission. During hospitalization, fever, splenomegaly, ascites, and pancytopenia appeared. Serology for Leishmania by indirect immunofluorescence was negative. Then, bone biopsy and molecular testing for Leishmania diagnosed it as visceral leishmaniasis. Amphotericin therapy was initiated with resolution of fever after 4 days of treatment and gradual recovery from pancytopenia. This case highlights the challenge of early diagnosis of visceral leishmaniasis in liver transplant recipients with diarrhea and leukopenia, which can be caused by immunosuppression or more prevalent viral diseases. Late onset of fever, splenomegaly, and a first negative serologic test also made early diagnosis difficult. The aim of the report is to emphasize the suspicion of visceral leishmaniasis in symptomatic patients from emerging countries and to question the benefit of including protozoan screening in liver transplant donors and recipients in endemic areas.

摘要

利什曼病是一种由原生动物引起的疾病,由几种新兴国家的沙蝇传播。内脏利什曼病是一种严重的并发症,特别是在免疫抑制患者中,在肝移植后并不常见。我们报告了一例 48 岁女性患者,因多囊肝而行肝移植。术后 6 个月,因腹泻、急性肾衰竭和白细胞减少症住院。她已经停用类固醇 3 个月,服用吗替麦考酚酯和他克莫司。她已经接受过巨细胞病毒的治疗,入院时结果为阴性。住院期间,出现发热、脾肿大、腹水和全血细胞减少。间接免疫荧光法检测利什曼血清学为阴性。随后,骨髓活检和利什曼分子检测诊断为内脏利什曼病。开始用两性霉素治疗,治疗 4 天后发热消退,全血细胞减少逐渐恢复。本病例强调了对腹泻和白细胞减少的肝移植受者进行早期诊断内脏利什曼病的挑战,这些症状可能是由免疫抑制或更常见的病毒疾病引起的。发热、脾肿大和首次阴性血清学检测的迟发性也使早期诊断变得困难。本报告的目的是强调对来自新兴国家的有症状患者怀疑患有内脏利什曼病,并质疑在流行地区对肝移植供体和受者进行原生动物筛查的益处。

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