医学
噬血细胞性淋巴组织细胞增多症
无症状的
内脏利什曼病
全血细胞减少症
儿科
噬血作用
疾病
利什曼病
骨髓
病理
免疫学
作者
Geydson Silveira da Cruz,Amélia Ribeiro de Jesus,Roque Pacheco de Almeida,Mariana Porto
标识
DOI:10.4269/ajtmh.20-1435
摘要
Visceral leishmaniasis (VL) is a neglected tropical disease with more than 30,000 cases annually reported worldwide. In Brazil, about 3,700 cases are annually reported. The VL clinical presentation is variable, from asymptomatic to severe cases with a high risk of death. We reported three cases of VL with clinical sign similarities but distinct development. All cases had bone marrow hemophagocytosis and hemophagocytic lymphohistiocytosis (HLH) criteria. HLH is a rare condition that may have secondary causes, including infectious and parasitic diseases, like VL. The delayed recognition of the secondary HLH (sHLH) association to VL may cause unfavorable outcomes and death.
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