首页|期刊导航|临床误诊误治|输入性内脏利什曼病误诊误治致多器官衰竭合并噬血细胞综合征病例分析

输入性内脏利什曼病误诊误治致多器官衰竭合并噬血细胞综合征病例分析OA

Misdiagnosis and mistreatment of imported visceral leishmaniasis leading to multiple organ failure complicated by hemophagocytic lymphohistiocytosis:A case analysis

中文摘要英文摘要

目的 探讨输入性内脏利什曼病(VL)误诊误治致多器官衰竭(MOF)合并噬血细胞综合征(HLH)的诊治经过,分析多重困境下采用普通两性霉素B救治的有效性和安全性,为临床类似VL的诊治提供参考.方法 回顾性分析2023年3月诊治的1例因"脾大"误诊误治,最终确诊为输入性VL合并HLH和MOF患者的临床资料.结果 患者以"脾大"为首发症状,多次就医,后因腹胀,伴呼吸困难及不明原因发热,诊断为"脾功能亢进、自身免疫性肝病、三系减少".在未明确病因的情况下,行脾动脉栓塞导致脾梗死,病情进一步加重至MOF;经流行病学史询问、骨髓穿刺、外周血镜检及多学科会诊后诊断为输入性VL合并HLH及MOF.误诊时间为2个月.给予普通两性霉素B剂量爬坡方案成功治疗,患者好转出院,随访2年未复发.结论 对于不明原因脾大患者,应详细询问流行病学史,早期行病原学检查,定期随访,避免误诊误治.在VL及合并相关并发症患者的临床治疗中,普通两性霉素B剂量爬坡方案可作为优选方案,其疗效确切,不良反应可控,具有良好的临床价值.

Objective To investigate the diagnosis and treatment process of visceral leishmaniasis(VL)misdiagnosed and mismanaged leading to multiple organ failure(MOF)combined with hemophagocytic lymphohistiocytosis(HLH),to analyze the effectiveness and safety of using conventional Amphotericin B for treatment under multiple dilemmas,so as to provide reference for the diagnosis and treatment of diseases similar to VL in clinical practice.Methods A retrospective analysis was conducted on the clinical data of a patient diagnosed and treated in March 2023 for splenomegaly,who was misdiagnosed and mistreated,and was ultimately confirmed to have imported VL combined with HLH and MOF.Results The patient presented with splenomegaly as the initial symptom and sought medical treatment repeatedly.Later,due to abdominal distension,accompanied by breathing difficulties and unexplained fever,the patient was diagnosed with hypersplenism,autoimmune liver disease,and pancytopenia.Without a clear cause identified,the patient underwent splenic artery embolization to cause splenic infarction,and the condition further deteriorated to MOF.After inquiries about the epidemiological history,bone marrow puncture,peripheral blood examination,and multidisciplinary consultation,it was diagnosed as imported VL combined with HLH and MOF.The misdiagnosis period was 2 months.The patient was successfully treated with a gradual dose-escalation regimen of conventional Amphotericin B,was discharged after recovery.Follow-up for 2 years showed no recurrence.Conclusion For patients with unexplained splenomegaly,a detailed epidemiological history should be taken,early etiological examinations should be performed,and regular follow-up should be ensured to avoid misdiagnosis and mistreatment.In the clinical treatment of VL and patients with related complications,a gradual dose-escalation regimen of conventional Amphotericin B can be used as the preferred scheme,with definite efficacy,controllable adverse reactions,and good clinical value.

朱先;吴娴;周明玉;杨黄燕;张宝芳;张权;陆爽

贵州医科大学临床医学院,贵阳 550002贵州医科大学附属医院感染科,贵阳 550002贵州医科大学附属医院感染科,贵阳 550002贵州医科大学临床医学院,贵阳 550002贵州医科大学附属医院感染科,贵阳 550002贵州医科大学附属医院感染科,贵阳 550002贵州医科大学临床医学院,贵阳 550002||贵阳市第二人民医院(金阳医院)/贵州医科大学附属金阳医院感染科,贵阳 550081

内脏利什曼病多器官衰竭噬血细胞综合征误诊脾功能亢进两性霉素B多学科诊疗

visceral leishmaniasismultiple organ failurehemophagocytic lymphohistiocytosismisdiagnosishypersplenismAmphotericin Bmultidisciplinary diagnosis and treatment

《临床误诊误治》 2026 (7)

1-7,7

国家自然科学基金资助项目(82260132)北京肝胆相照公益基金会项目(iGandanF-1082025-LG032)

10.3969/j.issn.1002-3429.2026.07.001

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