Rheumatology Section, Hospital Universitari Germans Trias I Pujol, Ctra del Canyet s/n, 08916 Badalona, Spain.
Joint Bone Spine. 2010 May;77(3):271-3. doi: 10.1016/j.jbspin.2010.01.011. Epub 2010 Apr 7.
Visceral leishmaniasis is a protozoan infection usually asymptomatic, but can progress to fatal disease in immunocompromised hosts, especially in HIV patients. Visceral leishmaniasis is rare among patients under immunosuppressive therapies, and even more among patients under anti-TNF-alpha treatment, where only four cases have been described.
Visceral leishmaniasis was established by bone marrow aspiration, and although there was no histological confirmation, according to HLH-2004 criteria, a secondary macrophagic activation syndrome was established. The patient had a favourable outcome.
We report herein the fifth case of visceral leishmaniasis in a patient under TNF-alpha therapy, and the first one, to our knowledge, presenting a consequent secondary macrophagic activation syndrome.
内脏利什曼病是一种原生动物感染,通常无症状,但在免疫功能低下的宿主中,特别是在 HIV 患者中,可进展为致命疾病。在接受免疫抑制治疗的患者中,内脏利什曼病很少见,在接受抗 TNF-α治疗的患者中甚至更为罕见,仅有 4 例被描述过。
1)描述一名接受阿达木单抗治疗的类风湿关节炎患者,该患者出现发热、全血细胞减少、脾肿大和极度高铁蛋白血症。2)通过在 PubMed 中进行搜索(1991-2008 年期间),回顾已发表的内脏利什曼病和抗 TNF-α治疗病例,以及利什曼病和巨细胞活化综合征并存的病例。
骨髓抽吸术确立了内脏利什曼病的诊断,尽管没有组织学证实,但根据 HLH-2004 标准,确立了继发性巨细胞活化综合征。患者的结局良好。
我们在此报告了第五例接受 TNF-α治疗的患者发生内脏利什曼病,据我们所知,这也是首例继发巨细胞活化综合征的病例。