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鲁索替尼联合两性霉素 B 治疗复发性利什曼病相关噬血细胞性淋巴组织细胞增多症有效: 一病例报告及文献复习
Received 16 August 2022
Accepted for publication 19 October 2022
Published 11 November 2022 Volume 2022:15 Pages 6625—6629
DOI https://doi.org/10.2147/IDR.S384628
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Professor Héctor M Mora-Montes
Background: Hemophagocytic lymphohistiocytosis (HLH) is known as a life-threatening syndrome, and Leishmania is the most common protozoan that triggers infection-related HLH. It is thus important to find the root cause and treat it effectively.
Case Report: This paper reports a 44-year-old man who developed antisynthetase antibody syndrome previously. The patient progressed rapidly to the extent of meeting the HLH-2004 diagnostic criteria, despite the unknown etiology. Although the patient was promptly treated in line with the HLH-1994 protocol to achieve remission, he still relapsed after glucocorticoid reduction. Afterwards, it was found out that HLH was secondary to Leishmania infection. The symptoms of HLH were alleviated quickly by the treatment with Ruxolitinib and Amphotericin B.
Conclusion: Etiological screening plays a crucial role in leishmaniasis-related HLH. An experienced pathologist and real-time PCR are essential for treating Leishmania . The treatment of Ruxolitinib and Amphotericin B proved effective in alleviating the relapse of visceral leishmaniasis-related HLH.
Keywords: hemophagocytic lymphohistiocytosis, visceral leishmaniasis, Amphotericin B, Ruxolitinib