Hepatic haemophagocytosis in haematology patients with hepatic dysfunction: prognostic impact and contribution of liver biopsy combined with the haemophagocytic syndrome diagnostic score (HScore)
- PMID: 35968907
- PMCID: PMC9805208
- DOI: 10.1111/bjh.18382
Hepatic haemophagocytosis in haematology patients with hepatic dysfunction: prognostic impact and contribution of liver biopsy combined with the haemophagocytic syndrome diagnostic score (HScore)
Abstract
Hepatic dysfunction (HD) is common in patients with haematological malignancies. Hepatic haemophagocytosis (HH) was detected in >50% of liver biopsies taken when HD remained unresolved after standard examination. We aimed to explore the contribution of liver biopsy in patients with both haematological malignancies and HD, describe the population of patients with HH, assess the prognostic impact of HH, and investigate haemophagocytic syndrome diagnostic score (HScore) utility in patients with HH. Between 2016 and 2019, 116 consecutive liver biopsies (76 transjugular, 40 percutaneous) were taken in 110 patients with haematological malignancy and HD (hyperbilirubinaemia, elevated transaminases, and/or cholestasis) and without a clear diagnosis. Liver biopsies were safe and diagnostically efficient. Predominant diagnoses included: HH (56%), graft-versus-host disease (55%), associated infections (24%), sinusoidal obstruction syndrome (15%), and tumoral infiltration (8%). Of patients, 35% were critically ill and 74% were allogeneic haematopoietic stem cell transplantation recipients, while 1-year overall survival (OS) was 35% with HH versus 58% without HH (p = 0.026). The 1-year OS was 24% with a HScore of ≥169 versus 50% with a HScore of <169 (p = 0.019). Liver biopsies are feasible in and contribute significantly to haematology patients with HD. HH occurred frequently and was associated with a poor prognosis. Combined with liver biopsy, the HScore may be helpful in refining haemophagocytic syndrome diagnosis.
Keywords: HScore; haemophagocytic syndrome; hepatic dysfunction; hepatic haemophagocytosis; liver biopsy.
© 2022 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.
Conflict of interest statement
The authors have no conflict of interest to declare.
Figures




Similar articles
-
Secondary haemophagocytic lymphohistiocytosis in COVID-19: correlation of the autopsy findings of bone marrow haemophagocytosis with HScore.J Clin Pathol. 2022 Jun;75(6):383-389. doi: 10.1136/jclinpath-2020-207337. Epub 2021 Mar 15. J Clin Pathol. 2022. PMID: 33722841
-
Correlation of haemophagocytosis with clinical criteria of haemophagocytic lymphohistiocytosis and recommendations for bone marrow reporting.Pathology. 2022 Jun;54(4):434-441. doi: 10.1016/j.pathol.2021.07.015. Epub 2021 Oct 26. Pathology. 2022. PMID: 34711415 Review.
-
Assessment of the HScore for reactive haemophagocytic syndrome in patients with rheumatic diseases.Scand J Rheumatol. 2017 Jan;46(1):44-48. doi: 10.3109/03009742.2016.1167951. Epub 2016 Jun 30. Scand J Rheumatol. 2017. PMID: 27359073
-
Diagnostic Performance of Hemophagocytic Lymphohistiocytosis Criteria and HScore in Critically Ill Patients With Severe Hemophagocytic Syndrome.Crit Care Med. 2021 Sep 1;49(9):e874-e879. doi: 10.1097/CCM.0000000000005038. Crit Care Med. 2021. PMID: 33852445
-
Pathology updates and diagnostic approaches to haemophagocytic lymphohistiocytosis.Histopathology. 2022 Mar;80(4):616-626. doi: 10.1111/his.14591. Epub 2022 Feb 10. Histopathology. 2022. PMID: 34716920 Review.
Cited by
-
Prognostic factors in patients with secondary hemophagocytic lymphohistioc ytosis in a Chinese cohort.Ann Hematol. 2024 Mar;103(3):695-703. doi: 10.1007/s00277-023-05567-x. Epub 2024 Jan 24. Ann Hematol. 2024. PMID: 38265737
References
-
- Barba P, Martino R, Perez‐Simón JA, Fernández‐Avilés F, Piñana JL, Valcárcel D, et al. Incidence, characteristics and risk factors of marked hyperbilirubinemia after allogeneic hematopoietic cell transplantation with reduced‐intensity conditioning. Bone Marrow Transplant. 2012;47(10):1343–9. - PubMed
-
- Subbarao G, Haut PR, Johnson CS, Gowan D, Molleston JP. Incidence, etiology, and risk factors for liver dysfunction in children following hematopoietic stem cell transplantation. Pediatr Transplant. 2006;10(6):682–9. - PubMed
-
- Van de Louw A, Twomey K, Habecker N, Rakszawski K. Prevalence of acute liver dysfunction and impact on outcome in critically ill patients with hematological malignancies: a single‐center retrospective cohort study. Ann Hematol. 2021;100(1):229–37. - PubMed
-
- Hogan WJ, Maris M, Storer B, Sandmaier BM, Maloney DG, Schoch HG, et al. Hepatic injury after nonmyeloablative conditioning followed by allogeneic hematopoietic cell transplantation: a study of 193 patients. Blood. 2004;103(1):78–84. - PubMed
-
- Bisbal M, Darmon M, Saillard C, Mallet V, Mouliade C, Lemiale V, et al. Hepatic dysfunction impairs prognosis in critically ill patients with hematological malignancies: a post‐hoc analysis of a prospective multicenter multinational dataset. J Crit Care. 2021;62:88–93. - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical