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Rare disease: Visceral leishmaniasis in immunosuppressed Caucasian patient

机译:罕见疾病:免疫抑制的白种人患者发生内脏利什曼病

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摘要

A 64-year-old man was admitted with fever, weight loss, fatigue and night sweats. He was known to have rheumatoid arthritis and had been taking methotrexate for 1 year. He had worked in Saudi Arabia until 1994 and had been living in Spain for 6 months every year. Clinical examination showed an enlarged spleen. Routine investigations showed pancytopaenia. Serial blood cultures were negative. CT scan confirmed splenomegaly and was otherwise unremarkable. Bone marrow biopsy revealed Leishmania amastigote consistent with a diagnosis of visceral leishmaniasis. After discussing with the hospital for tropical diseases (HTD), he was started on liposomal amphotericin B. Following two infusions of amphotericin B, he started improving as his fever, night sweats and weakness had settled. He was then discharged and followed up in HTD clinic 4 weeks later where he was found to be consistently improving.
机译:一名64岁的男子因发烧,体重减轻,疲倦和盗汗而入院。已知他患有类风湿关节炎,并已服用甲氨蝶呤一年。他一直在沙特阿拉伯工作到1994年,并且每年在西班牙居住6个月。临床检查显示脾脏肿大。常规检查显示全血细胞减少。连续血培养阴性。 CT扫描证实为脾肿大,否则无异常。骨髓活检显示利什曼原虫鞭毛体与内脏利什曼病的诊断一致。与热带病医院(HTD)讨论后,他开始使用脂质体两性霉素B。两次输注两性霉素B后,由于发烧,盗汗和虚弱无力,他开始好转。然后,他出院,并在4周后在HTD诊所接受随访,发现他一直在进步。

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