Case Report
Copyright ©The Author(s) 2023.
World J Clin Cases. Sep 16, 2023; 11(26): 6183-6188
Published online Sep 16, 2023. doi: 10.12998/wjcc.v11.i26.6183
Table 1 Diagnostic criteria of hemophagocytic lymphohistiocytosis: Hemophagocytic lymphohistiocytosis-2004
Criteria
Diagnosis will be established if one of either 1 or 2 below is fulfilled
AA molecular diagnosis consistent with HLH: Pathogenic mutations of PRF-1, UNC13D, STXBP2, Rab27a, STX11, SH2D1A, or XIAP
BDiagnostic criteria for HLH fulfilled (5 of 8 criteria below)
1Fever ≥ 38.5 C for ≥ 7 d
2Splenomegaly ≥ 3 finger breadth below left subcostal margin
3Cytopenia affecting ≥ 2 of 3 lineages in peripheral blood: Hemoglobin < 9 g/L; platelets < 100 × 109/L; absolute neutrophil count < 1.0 × 109/L
4Hypertriglyceridemia (> 265 mg/dL) and/or hypofibrinogenemia (< 150 mg/dL)
5Hemophagocytosis in bone marrow or spleen or lymph nodes or liver
6Low or absent natural killer cell activity
7Ferritin > 500 ng/mL
8Elevated soluble CD25 (sIL-2 receptor) ≥ 2400 U/mL
Table 2 Number of diagnostic criteria met, treatments, and outcomes
Case No
Diagnostic criteria met
Primary therapy
Outcome
11,2,3,4,5,7,8HLH-04Died
21,2,3,4,5,6,7HLH-04Survived
31,3,4,5,7,8HLH-04Survived
41,2,4,5,6,7,8HLH-94Survived
51,2,4,5,6,7,8HLH-94Survived
61,3,4,5,7HLH-94Died
71,2,4,6,7,8FDSurvived
81,2,4,5,6,7,8DEPSurvived
91,2,3,4,5,6,7,8HLH-94 with anakinraSurvived
101,2,3,4,5,7HLH-04Survived
111,2,3,4,7MethylprednisoloneSurvived