Hemophagocytic lymphohistiocytosis (HLH) is an uncommon disorder causing immune dysfunction in infants and young children. Many patients have an underlying immune disorder, although in some patients the underlying disorder is not known. Manifestations may include lymphadenopathy, hepatosplenomegaly, fever, and neurologic abnormalities. Diagnosis is by specific clinical and testing (genetic) criteria. Treatment is usually with chemotherapy and, in refractory cases or in cases with a genetic cause, hematopoietic stem cell transplantation.
(See also Overview of Histiocytic Syndromes.)
Hemophagocytic lymphohistiocytosis (HLH) is uncommon. It affects mostly infants < 18 months but can occur at any age. It involves a defect in targeted killing and the inhibitory controls of natural killer and cytotoxic T cells, resulting in excessive cytokine production and accumulation of activated T cells and macrophages in various organs. Cells in the bone marrow and/or spleen may attack red blood cells, white blood cells, and/or platelets.
HLH can be
Familial (primary)
Acquired (secondary)
HLH is diagnosed when patients fulfill at least 5 of the criteria described below or have a mutation in a known HLH-associated gene.
Acquired HLH can be associated with infections (eg, Epstein-Barr virus, cytomegalovirus, or others), cancer (eg, leukemias, lymphomas), immune disorders (eg, systemic lupus erythematosus, rheumatoid arthritis, polyarteritis nodosa, sarcoidosis, progressive systemic sclerosis, Sjögren syndrome, Kawasaki disease) and can occur in kidney or liver transplant recipients.
In both familial and acquired forms, clinical manifestations are similar.
Symptoms and Signs of HLH
Common manifestations of hemophagocytic lymphohistiocytosis include fever, hepatomegaly, splenomegaly, rash, lymphadenopathy, and neurologic abnormalities (eg, seizures, retinal hemorrhages, ataxia, altered consciousness or coma).
Diagnosis of HLH
Clinical and testing criteria
Hemophagocytic lymphohistiocytosis can be diagnosed if there is a mutation in a known causative gene or if at least 5 of 8 diagnostic criteria based on HLH-2004 protocol (1) are met:
Fever (peak temperature of > 38.5° C for > 7 days)
Splenomegaly (spleen palpable > 3 cm below costal margin)
Cytopenia involving > 2 cell lines (hemoglobin < 9 g/dL [90 g/L], absolute neutrophil count < 100/mcL [0.10 × 109/L], platelets < 100,000/mcL [100 × 109/L])
Hypertriglyceridemia (fasting triglycerides > 177 mg/dL [2.0 mmol/L] or > 3 standard deviations [SD] more than normal value for age) or hypofibrinogenemia (fibrinogen < 150 mg/dL [1.5 g/L] or > 3 SD less than normal value for age)
Hemophagocytosis (in biopsy samples of bone marrow, spleen, or lymph nodes)
Low or absent natural killer cell activity
Serum ferritin > 500 ng/mL (> 1123.5 pmol/Lng/mL)
Elevated soluble interleukin-2 (CD25) levels (>2400 U/mL or very high for age)
Genetic mutations associated with HLH include
PRF1
RAB27
STX11
STXBP2
UNC13D
XLP
Because some of these tests may not be widely available and HLH is uncommon, patients are usually referred to specialized centers for evaluation. Genetic testing is recommended to look for primary HLH mutations as well as mutations that characterize immune dysregulation. Familial and acquired forms are differentiated only by family history.
Довідковий матеріал щодо діагностики
1. Henter JI, Horne A, Aricó M, et al: HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer 48(2):124–131, 2007. doi: 10.1002/pbc.21039
Treatment of HLH
Chemotherapy, cytokine inhibitors, immune suppression, and sometimes hematopoietic stem cell transplantation
Treatment for hemophagocytic lymphohistiocytosis should be started if the disorder is suspected, even if not all diagnostic criteria are fulfilled. Patients are usually treated by a pediatric hematologist and in a referral center experienced in treating patients with HLH. Treatment depends on the presence of factors such as a family history of HLH, coexisting infections, and demonstrated immune system defects. Treatment for HLH may include cytokine inhibitors, immune therapy, chemotherapy, some combination of these, and possibly stem cell transplantation.
A response to early initiation of anakinra (IL1 antagonist) in patients with secondary HLH has been reported and may allow for avoidance of intensive chemotherapy but requires further investigation (1). Ruxolitinib (a JAK-STAT pathway inhibitor) for upfront treatment of HLH is being explored in a clinical trial sponsored by the North American Consortium for Histiocytosis (NACHO).
Emapalumab, an interferon gamma–blocking monoclonal antibody, is available for patients with refractory, recurrent, or progressive HLH or with an intolerance to conventional therapy.
Довідковий матеріал щодо лікування
1. Bami S, Vagrecha A, Soberman D, et al: The use of anakinra in the treatment of secondary hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer 67(11):e28581, 2020. doi: 10.1002/pbc.28581
Ключові моменти
Hemophagocytic lymphohistiocytosis (HLH) is an uncommon rare disorder and usually affects infants < 18 months.
HLH can be familial (inherited) or acquired.
Diagnose HLH if the patient has at least 5 of 8 published diagnostic criteria or if the patient has a known mutation associated with HLH.
Treat with chemotherapy, cytokine inhibitors, immune suppression, and sometimes hematopoietic stem cell transplantation.
Додаткова інформація
The following are some English-language resources that may be useful. Please note that THE MANUAL is not responsible for the content of these resources.
Canna SW, Marsh RA: Pediatric hemophagocytic lymphohistiocytosis. Blood 135(16):1332–1343, 2020. doi: 10.1182/blood.2019000936
Histiocyte Society: International society for research into treatment of histiocytic diseases
North American Consortium for Histiocytosis: Conducts clinical and translational studies on histiocytosis and supports researchers and clinicians working in the field
