Alexandropoulou Ourania, Tsolia Maria, Kossiva Lydia, Giannaki Maria, Karavanaki Kyriaki
2nd Department of Pediatrics, University of Athens, Greece.
Pediatr Emerg Care. 2012 Jun;28(6):533-7. doi: 10.1097/PEC.0b013e3182587d5d.
Visceral leishmaniasis (VL, kala-azar) is caused by Leishmania spp, a parasite that is commonly encountered in Mediterranean countries. Leishmaniasis usually presents with fever, hepatosplenomegaly, lymphadenopathy, and pancytopenia.
The aim of the study was to prospectively examine the characteristics of cytopenia associated with VL and compare it with other post-infectious cytopenias observed in children with febrile illnesses.
We studied 112 children, aged (mean) 4.0 (SD, 3.8) years (range, 0-14 years), who were admitted to the pediatric ward because of febrile cytopenia associated with infections, during a 2-year period (March 2005 to June 2007). Study participants were investigated with measurement of acute-phase reactants, bacterial cultures, and serologic tests.
Pancytopenia was detected in 9 (8%) of 112 patients (5 boys), with a mean age of 4.5 (SD, 3.0) years.The mean value of white blood cell was 3827 (SD, 1455)/mL; absolute neutrophil count, 1229 (SD, 655)/mL; hemoglobin, 8.3 (SD, 1.1) g/dL; and platelet count, 88,200 (SD, 20,186)/mL. All patients with pancytopenia had fever (mean duration, 8.9 [SD, 8.7] days) (maximum temperature, 39.5°C [SD, 0.6°C]) and hepatosplenomegaly (9/9), whereas 2 of 9 had lymphadenopathy. In these patients, a bone marrow aspiration was performed, and VL was detected in all 9 samples. They were treated with liposomal amphotericin B and had an excellent response rate. Pancytopenia resolved within a mean period of 17.6 (SD, 17.3) days (range, 8-60 days), and there was no relapse during a 2 years' follow-up.
In endemic countries, leishmaniasis is the main cause of febrile pancytopenia among children in whom hematologic malignancy has been ruled out.
内脏利什曼病(VL,黑热病)由利什曼原虫属引起,这种寄生虫在地中海国家较为常见。利什曼病通常表现为发热、肝脾肿大、淋巴结病和全血细胞减少。
本研究旨在前瞻性地研究与VL相关的血细胞减少的特征,并将其与发热性疾病患儿中观察到的其他感染后血细胞减少进行比较。
我们研究了112名儿童,年龄(平均)为4.0(标准差,3.8)岁(范围为0至14岁),他们在2年期间(2005年3月至2007年6月)因与感染相关的发热性血细胞减少而入住儿科病房。对研究参与者进行了急性期反应物测量、细菌培养和血清学检测。
112名患者中有9名(8%)(5名男孩)检测到全血细胞减少,平均年龄为4.5(标准差,3.0)岁。白细胞平均值为3827(标准差,1455)/mL;绝对中性粒细胞计数为1229(标准差,655)/mL;血红蛋白为8.3(标准差,1.1)g/dL;血小板计数为88,200(标准差,20,186)/mL。所有全血细胞减少的患者均有发热(平均持续时间,8.9[标准差,8.7]天)(最高体温,39.5°C[标准差,0.6°C])和肝脾肿大(9/9),而9名患者中有2名有淋巴结病。对这些患者进行了骨髓穿刺,所有9份样本均检测到VL。他们接受了脂质体两性霉素B治疗,反应率极佳。全血细胞减少在平均17.6(标准差,17.3)天(范围为8至60天)内得到缓解,在2年的随访期间无复发。
在流行国家,利什曼病是排除血液系统恶性肿瘤的儿童发热性全血细胞减少的主要原因。