怀疑意外:自身免疫性溶血性贫血和嗜血细胞淋巴组织细胞增多症与内脏利什曼病的罕见关联:病例报告和文献综述。

Q2 Medicine Electronic Journal of the International Federation of Clinical Chemistry and Laboratory Medicine Pub Date : 2023-12-21 eCollection Date: 2023-12-01
Aman Elwadhi, Neha Kc, Kamal Joshi, G Krishna Charan
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引用次数: 0

摘要

内脏利什曼病是一种常见的热带传染病,表现为多种血液学异常。我们报告了一例不寻常的病例:一名 11 岁女孩发热,伴有肝脾肿大和贫血。实验室检查结果包括全血细胞减少和高胆红素血症。利什曼病抗原 rK39 呈阳性,骨髓检查显示有嗜血细胞增多症和纺锤体形式的多诺万利什曼病。直接库姆斯氏试验呈阳性(温热型,IgG),低密度脂蛋白胆固醇(LDH)升高。其他感染检测结果均为阴性。诊断结果为内脏利什曼病合并自身免疫性溶血性贫血(温抗体型,IgG)和嗜血细胞淋巴组织细胞增多症。患者在接受抗利什曼病治疗后病情有所好转。
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Suspect the Unexpected: A Rare Association of Autoimmune Hemolytic Anemia and Hemophagocytic Lymphohistiocytosis with Visceral Leishmaniasis: A Case Report and Review of Literature.

Visceral leishmaniasis is a common tropical infection presenting with a myriad of hematological abnormalities. We report an unusual case of an 11-year-old girl suffering from a febrile illness with hepatosplenomegaly and anemia. Laboratory findings included pancytopenia and hyperbilirubinemia. The leishmania antigen rK39 was positive and bone marrow examination revealed hemophagocytosis and amastigote forms of Leishmania donovani. Direct Coombs' test was positive (warm type, IgG) and LDH was elevated. Tests for other infections were negative. A diagnosis of visceral leishmaniasis with autoimmune hemolytic anemia (warm antibody type, IgG) with hemophagocytic lymphohistiocytosis was made. Patient showed response with anti-leishmanial treatment with improvement in clinical condition.

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