Infectious Diseases and Immunology Department, Oeste Paulista University, Presidente Prudente, São Paulo, Brazil.
Imunodeficiencies Outpatient Clinic, Pediatrics Outpatient Clinic, Regional Hospital of Presidente Prudente, Presidente Prudente, São Paulo, Brazil.
BMC Infect Dis. 2019 Jan 18;19(1):70. doi: 10.1186/s12879-018-3652-1.
Visceral leishmaniasis (VL) is becoming endemic in São Paulo state, in the southeastern region of Brazil. Unusual manifestations with non-specific signs and symptoms may make diagnosis difficult and delay treatment, increasing the risk of severity and death, particularly in new endemic areas. There are few studies on patients with these characteristics in Brazil. We describe a case series of unusual manifestations of VL in children and its spatial dispersion in the western region of São Paulo state.
From 2009 to 2014, five clinical cases involving children treated in the Regional Hospital of Presidente Prudente (RH) were selected. Two patients had multiple relapses requiring liposomal amphotericin B; one patient had VL-cytomegalovirus-dengue co-infection and liver injury; one patient was diagnosed with X-linked agammaglobulinemia, a primary immunodeficiency; and one patient was diagnosed with VL-human immunodeficiency virus/acquired immunodeficiency syndrome (VL-HIV/AIDS) co-infection. Primary or secondary immunodeficiencies were found in four children, and associated viral infections were found in three children. Three patients were referred from other hospitals to RH. With regard to the geographic spread of VL, more cases were found in the northern area, in the epicenter of the infection where the first cases were registered, flowing south; a spatial-temporal occurrence was found.
Primary and secondary immunodeficiencies and viral co-infectious should be considered among unusual manifestations of VL, especially in those with multiple relapses. Spatial-temporal occurrence was found. Thus, integrated actions and effective monitoring of the disease are needed to complement curative practices to stem the tide of the epidemic.
内脏利什曼病(VL)在巴西东南部的圣保罗州呈地方性流行。不典型表现伴非特异性体征和症状可能使诊断变得困难,并导致治疗延迟,增加严重程度和死亡的风险,尤其是在新的地方性流行地区。巴西有关此类特征患者的研究较少。我们描述了圣保罗州西部地区儿童内脏利什曼病不典型表现的病例系列及其空间分布。
2009 年至 2014 年,选择了在总统普鲁登特地区医院(RH)接受治疗的 5 例临床病例。2 例患者有多次复发,需要使用脂质体两性霉素 B;1 例患者同时感染了内脏利什曼病-巨细胞病毒-登革热;1 例患者诊断为 X 连锁无丙种球蛋白血症,即原发性免疫缺陷;1 例患者诊断为内脏利什曼病-人类免疫缺陷病毒/获得性免疫缺陷综合征(VL-HIV/AIDS)合并感染。4 例患儿存在原发性或继发性免疫缺陷,3 例患儿存在相关病毒感染。3 例患者从其他医院转诊至 RH。就 VL 的地理分布而言,在感染的震中即北部地区发现了更多病例,从北部向南部流动,呈现时空发生。
在 VL 的不典型表现中,尤其是在多次复发的情况下,应考虑原发性和继发性免疫缺陷以及病毒合并感染。呈现时空发生。因此,需要采取综合行动和有效监测疾病,以补充治疗措施,遏制疫情蔓延。