Chouchene S, Braham N, Bouatay A, Hizem S, Berriri S, Eljemai A, Boughamoura L, Kortas M
Laboratoire d'hématologie, hôpital Farhat Hached, 4000 Sousse, Tunisie.
Laboratoire d'hématologie, hôpital Farhat Hached, 4000 Sousse, Tunisie.
Arch Pediatr. 2015 Nov;22(11):1107-11. doi: 10.1016/j.arcped.2015.08.012.
The clinical and biological manifestations of visceral leishmaniasis are often confusing, most particularly because it can mimic and lead to a variety of hematological disorders. The aim of this study was to investigate the hematologic abnormalities observed in infantile visceral leishmaniasis from January 2000 and December 2013. The study included 35 children with a mean age of 3.5 years. Clinical manifestations were dominated by splenomegaly, fever, and paleness, defining the classic triad in 16% of our patients. Anemia was present in all patients. Leukopenia was found in 51% of the cases. Thrombocytopenia was observed in 48% of our patients and 36% had pancytopenia. All cases were confirmed by the presence of Leishman bodies (amastigotes) in the bone marrow smears. Quantitative and qualitative megakaryocyte abnormalities were found. Similarly, dysgranulopoiesis was observed in 31% of the cases, eosinophilia was present in 6%, erythroid hypoplasia in 3%, and erythroid hyperplasia in 34%. Different features of dyserythropoiesis were revealed in 71% of the patients with images of hemophagocytosis in 6% and multiple dysplasias in 9%. The knowledge of these hematological abnormalities associated with infantile visceral leishmaniasis can assist us in searching for Leishman bodies in the bone marrow smears to provide a diagnosis more quickly without necessarily resorting to more sophisticated tests.
内脏利什曼病的临床和生物学表现常常令人困惑,尤其是因为它可以模仿并导致多种血液系统疾病。本研究的目的是调查2000年1月至2013年12月期间在婴儿内脏利什曼病中观察到的血液学异常。该研究纳入了35名平均年龄为3.5岁的儿童。临床表现以脾肿大、发热和面色苍白为主,16%的患者出现了典型的三联征。所有患者均存在贫血。51%的病例发现白细胞减少。48%的患者观察到血小板减少,36%的患者出现全血细胞减少。所有病例均通过骨髓涂片发现利什曼小体(无鞭毛体)得以确诊。发现了巨核细胞的定量和定性异常。同样,31%的病例观察到粒细胞生成异常,6%的病例出现嗜酸性粒细胞增多,3%的病例出现红系造血低下,34%的病例出现红系造血增生。71%的患者出现了不同特征的红细胞生成异常,6%的患者出现噬血细胞图像,9%的患者出现多种发育异常。了解这些与婴儿内脏利什曼病相关的血液学异常有助于我们在骨髓涂片中寻找利什曼小体,从而更快地做出诊断,而不必借助更复杂的检查。