Case report: Infection-associated HPS during pregnancy cured by HLH-94 protocol with induction therapy of ruxolitinib

Hemophagocytic syndrome (HPS) is a rapidly progressive and highly fatal disease, and is even more complex when it occurs during pregnancy. Currently, the HLH-94 protocol is commonly used for treatment for HPS, with ruxolitinib being mostly used for salvage therapy. Here, we report a pregnant woman who presented with fever, thrombocytopenia, splenomegaly, and subsequently developed into severe pneumonia and multiple organ dysfunction(MODS). The patient was diagnosed as HPS based on clinical manifestations, laboratory indexes, and hemophagocytosis observed in bone marrow aspirate smear. After receiving ruxolitinib as induction therapy combined with HLH-94 protocol, the patient significantly improved and eventually cured.

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Publication Details

Journal
Frontiers in Immunology
Published
2024-11-15
DOI
https://doi.org/10.3389/fimmu.2024.1483257
Citations
3
Primary Topic
Autoimmune and Inflammatory Disorders Research
Type
article
Field-Weighted Citation Impact
1.36
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article

Case report: Infection-associated HPS during pregnancy cured by HLH-94 protocol with induction therapy of ruxolitinib

Weixia Xuan, Jian‐Pei Fang, Shenying Yang, Ziqi Wang et al.
3 citations
Frontiers in Immunology
Autoimmune and Inflammatory Disorders Research
1.36
article

Case report: Infection-associated HPS during pregnancy cured by HLH-94 protocol with induction therapy of ruxolitinib

Weixia Xuan, Jian‐Pei Fang, Shenying Yang, Ziqi Wang, Moyuan Zhang, Lijun Shen, Xiaoju Zhang, Shaohui Huang, Tianqi Cen
article en
3 citations

Abstract

Hemophagocytic syndrome (HPS) is a rapidly progressive and highly fatal disease, and is even more complex when it occurs during pregnancy. Currently, the HLH-94 protocol is commonly used for treatment for HPS, with ruxolitinib being mostly used for salvage therapy. Here, we report a pregnant woman who presented with fever, thrombocytopenia, splenomegaly, and subsequently developed into severe pneumonia and multiple organ dysfunction(MODS). The patient was diagnosed as HPS based on clinical manifestations, laboratory indexes, and hemophagocytosis observed in bone marrow aspirate smear. After receiving ruxolitinib as induction therapy combined with HLH-94 protocol, the patient significantly improved and eventually cured.

Frontiers in ImmunologyVol. 15
Zhengzhou University (CN), Henan Provincial People's Hospital (CN), Henan Medical University (CN)
Good health and well-being
Openalex Percentile: Top 17%
Autoimmune and Inflammatory Disorders Research
1.36
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