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Hemophagocytic lymphohistiocytosis induced by radio-chemo-immunotherapy: a case report.

증례보고 3/5 보강
Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] 📖 저널 OA 51.9% 2021: 1/1 OA 2022: 1/1 OA 2025: 4/13 OA 2026: 22/37 OA 2021~2026 2026 Vol.202(5) p. 539-543 cited 3 OA Autoimmune and Inflammatory Disorder
TL;DR This case highlights the importance of early recognition and aggressive management of HLH secondary to immunotherapy, particularly in patients presenting with unexplained fever, G-CSF-refractory cytopenia, and hyperferritinemia.
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PubMed DOI PMC OpenAlex Semantic 마지막 보강 2026-04-28
연도별 인용 (2025–2026) · 합계 3
OpenAlex 토픽 · Autoimmune and Inflammatory Disorders Research Immune Cell Function and Interaction CNS Lymphoma Diagnosis and Treatment

Salazar-Zuniga B, Thurner L, Mohr T, Staber P, Hecht M, Fleser O

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This case highlights the importance of early recognition and aggressive management of HLH secondary to immunotherapy, particularly in patients presenting with unexplained fever, G-CSF-refractory cytop

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APA Bryan Salazar-Zuniga, Lorenz Thurner, et al. (2026). Hemophagocytic lymphohistiocytosis induced by radio-chemo-immunotherapy: a case report.. Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al], 202(5), 539-543. https://doi.org/10.1007/s00066-025-02478-w
MLA Bryan Salazar-Zuniga, et al.. "Hemophagocytic lymphohistiocytosis induced by radio-chemo-immunotherapy: a case report.." Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al], vol. 202, no. 5, 2026, pp. 539-543.
PMID 41083745 ↗

Abstract

[BACKGROUND] Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory syndrome characterized by supramaximal immune activation. Although rare, HLH has been increasingly recognized as an immune-related adverse event in patients undergoing immune checkpoint inhibitor (ICI) therapy.

[CASE PRESENTATION] We report the case of a female patient treated with concomitant radio-chemo-immunotherapy for cervical cancer (according to the KEYNOTE-A18 trial). She developed HLH following a single dose of pembrolizumab, presenting initially with immune-mediated pneumonitis and subsequently with fever, prolonged pancytopenia, and elevated inflammatory markers. After intensive diagnostics, broad-spectrum anti-infective treatment and granulocyte colony-stimulating factor (G-CSF) stimulation was started, without improvement. The diagnosis was finally made by HLH-2004 criteria, strongly indicated by an H‑score of 251 (> 99% probability of HLH). The HLH was successfully treated with corticosteroids alone.

[CONCLUSION] This case highlights the importance of early recognition and aggressive management of HLH secondary to immunotherapy, particularly in patients presenting with unexplained fever, G‑CSF-refractory cytopenia, and hyperferritinemia.

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🏷️ 같은 키워드 · 무료전문 — 이 논문 MeSH/keyword 기반

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