Badaro R, Jones T C, Carvalho E M, Sampaio D, Reed S G, Barral A, Teixeira R, Johnson W D
J Infect Dis. 1986 Dec;154(6):1003-11. doi: 10.1093/infdis/154.6.1003.
During an epidemiological study of visceral leishmaniasis in an endemic region of Brazil, new perspectives emerged on a subclinical form of the disease. A group of 86 children with antibody to Leishmania were identified. None of these children had a history of leishmaniasis. The children were segregated into four groups: One group remained asymptomatic (n = 20), whereas another developed classic kala-azar within weeks of the index serology (n = 15). The remaining 51 patients initially had subclinical disease; 13 (25%) of these patients progressed to classic kala-azar (mean, five months). The others (75%) resolved their illness after a prolonged period (mean, 35 months). The initial illness in the subclinical group was characterized by hepatomegaly, frequent splenomegaly, intermittent cough, diarrhea, and low-grade fever. Malaise and poor weight gain were common. Giemsa-stained smears and cultures of bone marrow aspirates were usually negative for Leishmania in the absence of symptoms of classic kala-azar.
在巴西一个内脏利什曼病流行地区进行的一项流行病学研究中,该疾病的亚临床形式出现了新的情况。确定了一组86名携带利什曼原虫抗体的儿童。这些儿童均无利什曼病病史。这些儿童被分为四组:一组仍无症状(n = 20),而另一组在首次血清学检测后的几周内发展为典型的黑热病(n = 15)。其余51名患者最初患有亚临床疾病;其中13名(25%)患者进展为典型的黑热病(平均5个月)。其他患者(75%)在较长一段时间后(平均35个月)病情得到缓解。亚临床组的初始疾病表现为肝肿大、频繁脾肿大、间歇性咳嗽、腹泻和低热。全身不适和体重增加不佳很常见。在没有典型黑热病症状的情况下,吉姆萨染色涂片和骨髓穿刺培养通常未发现利什曼原虫。