Haemophagocytic lymphohistiocytosis and abdominal compartment syndrome in acute pancreatitis
Haemophagocytic lymphohistiocytosis (HLH) is a rare and often fatal syndrome that may be primary or secondary. This is a case of HLH associated with necrotizing pancreatitis, complicated by abdominal compartment syndrome. It highlights the need for high degree of suspicion for diagnosis in surgical patients, the complexity of managing the sequalae of HLH, and the importance of early treatment.
Authors
- Oliver M. Fisher (ORCID: https://orcid.org/0000-0001-9836-8636)
- Linda Y. Zhang (ORCID: https://orcid.org/0000-0001-6135-0563)
- Hasib Ahmadzai
- Aimee Hope (ORCID: https://orcid.org/0000-0002-8083-5811)
- Nishka Tapaswi
Institutions
- UNSW Sydney (AU)
- St George Hospital (AU)
- St. George Hospital (IN)
Publication Details
- Journal
- Journal of Surgical Case Reports
- Published
- 2025-09-30
- DOI
- https://doi.org/10.1093/jscr/rjaf813
- Primary Topic
- Muscle and Compartmental Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00