Department of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Key Laboratory of Birth Defects and Related Diseases of Women and Children, Sichuan University, Ministry of Education, Chengdu, Sichuan, China.
Front Public Health. 2023 Jun 22;11:1197149. doi: 10.3389/fpubh.2023.1197149. eCollection 2023.
Visceral leishmaniasis (VL) is a neglected vector-borne tropical disease caused by () and (). Due to the very small dimensions of the protozoa impounded within blood cells and reticuloendothelial structure, diagnosing VL remains challenging.
Herein, we reported a case of VL in a 17-month-old boy with acute lymphoblastic leukemia (ALL). The patient was admitted to West China Second University Hospital, Sichuan University, due to repeated fever after chemotherapy. After admission, chemotherapy-related bone marrow suppression and infection were suspected based on clinical symptoms and laboratory test results. However, there was no growth in the conventional peripheral blood culture, and the patient was unresponsive to routine antibiotics. Metagenomics next-generation sequencing (mNGS) of peripheral blood identified reads, followed by spp amastigotes using cytomorphology examination of the bone marrow specimen. The patient was given pentavalent antimonials as parasite-resistant therapy for 10 days. After the initial treatment, reads were still found in peripheral blood by mNGS. Subsequently, the anti-leishmanial drug amphotericin B was administrated as rescue therapy, and the patient was discharged after a clinical cure.
Our results indicated that leishmaniasis still exists in China. Unbiased mNGS provided a clinically actionable diagnosis of a specific infectious disease from an uncommon pathogen that eluded conventional testing.
内脏利什曼病(VL)是一种被忽视的热带病,由()和()引起。由于被禁锢在血细胞和网状内皮结构内的原生动物的体积非常小,因此诊断 VL 仍然具有挑战性。
在此,我们报告了一例 17 个月大的急性淋巴细胞白血病(ALL)合并 VL 的病例。该患者因化疗后反复发热而入住四川大学华西第二医院。入院后,根据临床症状和实验室检查结果,怀疑为化疗相关骨髓抑制和感染。然而,常规外周血培养无生长,且患者对常规抗生素无反应。外周血宏基因组下一代测序(mNGS)鉴定到 条读段,随后通过骨髓标本的细胞形态学检查发现 spp 无鞭毛体。给予患者五价锑剂进行寄生虫耐药治疗 10 天。初始治疗后,mNGS 仍在外周血中发现 条读段。随后,给予两性霉素 B 抗利什曼原虫药物进行挽救治疗,患者临床治愈后出院。
我们的结果表明,利什曼病在中国仍然存在。无偏倚的 mNGS 为一种罕见病原体引起的特定传染病提供了具有临床意义的诊断,该病原体逃避了常规检测。