Evidence map›Paper›PMID 42774303›Full record

ArticleFrontiers in immunology2026

Case Report: Definite DRESS following phenobarbital exposure with secondary HLH and DAT-positive hemolysis during high-dose IVIG treatment in a child.

Lingmei Zhang, Siyu Lei, Daiyu Zhang, Feng Chen, Qian Wan, Hong Wang, Zhongjin Xu, Chongjun Wu

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Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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8 authors.

Lingmei ZhangDepartment of Hematology, Jiangxi Provincial Children's Hospital, Nanchang, China.
Siyu LeiJiangxi Medical College, Nanchang University, Nanchang, China.
Daiyu ZhangJiangxi Medical College, Nanchang University, Nanchang, China.
Feng ChenDepartment of Hematology, Jiangxi Provincial Children's Hospital, Nanchang, China.
Qian WanDepartment of Hematology, Jiangxi Provincial Children's Hospital, Nanchang, China.
Hong WangDepartment of Hematology, Jiangxi Provincial Children's Hospital, Nanchang, China.
Zhongjin XuDepartment of Hematology, Jiangxi Provincial Children's Hospital, Nanchang, China.
Chongjun WuDepartment of Hematology, Jiangxi Provincial Children's Hospital, Nanchang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Drug reaction with eosinophilia and systemic symptoms (DRESS) is a severe delayed drug hypersensitivity reaction that may overlap with secondary hemophagocytic lymphohistiocytosis (HLH). Direct antiglobulin test (DAT)-positive hemolysis during intravenous immunoglobulin (IVIG) treatment creates an attribution problem because disease-associated autoimmune hemolysis and treatment-related passive red-cell sensitization or hemolysis may present similarly. Case presentation: A 13-year-and-5-month-old boy developed fever and a generalized pruritic eruption following phenobarbital exposure. A point-by-point RegiSCAR assessment yielded 6 points, classifying the presentation as definite DRESS. He fulfilled five HLH-2004 criteria, consistent with secondary HLH. The patient was blood group AB and RhD-positive, received no red-cell transfusions, and received 87.5 g of IVIG (approximately 2.0 g/kg). After 77.5 g had already been administered, dark urine was observed and DAT sampling was performed on hospital day (HD) 5 before the final 10 g IVIG infusion. Hemoglobin fell from 119 g/L on HD 2 to 86 g/L on HD 5 and reached 83 g/L on HD 7; indirect bilirubin increased, and DAT was immunoglobulin G (IgG) positive (1+) and C3d negative. DAT weakened on HD 9 and became negative on HD 13. Neither pre-IVIG DAT nor red-cell antibody screening was performed, and no subsequent antibody elution or specificity testing was available. Hemolysis profiling was further limited by the absence of haptoglobin measurements, peripheral-smear assessment, cold-antibody testing, and serial reticulocyte measurements. Withdrawal of suspected drugs, high-dose methylprednisolone followed by tapering, and supportive care were followed by sustained recovery without red-cell transfusion or HLH-specific cytotoxic therapy. Conclusion: This case suggests that, in a child with definite DRESS following phenobarbital exposure and secondary HLH, DAT-positive hemolysis is temporally associated with high-dose IVIG exposure, although the underlying mechanism remains unclear. Therefore, in similar clinical scenarios, we suggest documenting blood group, pre-IVIG DAT and antibody screening, and cumulative dose prospectively.

Indexed as

Drug Hypersensitivity SyndromeHemolysisImmunoglobulins, IntravenousLymphohistiocytosis, HemophagocyticPhenobarbitalAdolescentCoombs TestHumansMaleTreatment OutcomeImmunoglobulins, IntravenousPhenobarbitalcase reportDAT-positive hemolysisdressintravenous immunoglobulinsecondary hemophagocytic lymphohistiocytosis

Identifiers

PMID42774303
PMCPMC13593811

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