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      The Prognostic Significance of Beta2 Microglobulin in Patients with Hemophagocytic Lymphohistiocytosis

      research-article
      1 , 2 , 1 , *
      Disease Markers
      Hindawi Publishing Corporation

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          Abstract

          Objective. To determine the prognostic significance of beta2 microglobulin ( β 2-m) concentrations in patients with hemophagocytic lymphohistiocytosis (HLH), a rare disorder caused by pathologic activation of the immune system. Patients and Methods. The study population consisted of 74 patients diagnosed with HLH and 35 healthy controls. Serum β 2-m levels were measured using a latex agglutination photometric immunoassay. Results. Median serum β 2-m levels were significantly higher in HLH patients than in healthy controls (4.05 versus 1.5 mg/L; P < 0.001) and were significantly higher in patients with lymphoma associated hemophagocytic syndrome (LAHS) than in patients with benign disease-associated HLH (4.2 versus 3.3 mg/L; P < 0.001). Higher serum β 2-m levels were positively correlated with LAHS ( P = 0.005), abnormal lactate dehydrogenase concentrations ( P = 0.009), and hypoalbuminemia ( P = 0.003). ROC analysis showed that overall survival (OS) was significantly shorter in LAHS patients with serum β 2-m levels ≥4.03 mg/L compared to <4.03 mg/L ( P < 0.001). Moreover, multivariate analysis showed that serum β 2-m level was an independent prognostic of OS ( P = 0.034) in patients with LAHS. Conclusion. High serum β 2-m levels and LAHS were associated with markedly poorer OS in patients with HLH. Serum β 2-m concentration was a powerful and independent prognostic factor for OS in patients with LAHS.

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          Most cited references24

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          Nationwide survey of hemophagocytic lymphohistiocytosis in Japan.

          Hemophagocytic lymphohistiocytosis (HLH), a disorder of the mononuclear phagocyte system, can be classified into two distinct forms: primary HLH (FHL) and secondary HLH. To clarify the epidemiology and clinical outcome for each HLH subtype, we conducted a nationwide survey of HLH in Japan. Since 799 patients were diagnosed in 292 institutions of Japan between 2001 and 2005, the annual incidence of HLH was estimated as 1 in 800,000 per year. Among them, 567 cases were actually analyzed in this study. The most frequent subtype was Epstein-Barr virus (EBV)-associated HLH, followed by other infection- or lymphoma-associated HLH. Age distribution showed a peak of autoimmune disease- and infection-associated HLH in children, while FHL and lymphoma-associated HLH occurred almost exclusively in infants and the elderly, respectively. The 5-year overall survival rate exceeded 80% for patients with EBV- or other infection-associated HLH, was intermediate for those with FHL or B-cell lymphoma-associated HLH, and poor for those with T/NK cell lymphoma-associated HLH (<15%). Although this nationwide survey establishes the heterogeneous characteristics of HLH, the results should be useful in planning prospective studies to identify the most effective therapy for each HLH subtype.
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            Hemophagocytic syndromes.

            Hemophagocytic syndromes (hemophagocytic lymphohistiocytosis, HLH) represent a severe hyperinflammatory condition with the cardinal symptoms prolonged fever, cytopenias, hepatosplenomegaly, and hemophagocytosis by activated, morphologically benign macrophages. Biochemical markers include elevated ferritin and triglycerides, and low fibrinogen. Whereas in children several inherited immune deficiencies may lead to this syndrome, most adults with HLH have no known underlying immune defect. Nevertheless, impaired function of natural killer (NK) cells and cytotoxic T-cells (CTL) is characteristic for both genetic and acquired forms of HLH. Frequent triggers are infectious agents, mostly viruses of the herpes group. Malignant lymphomas, especially in adults, may be associated with HLH. A special form of HLH in rheumatic diseases is called macrophage-activation syndrome. Initially HLH may masquerade as a normal infection since all symptoms, even though less pronounced, may also be found in immune competent patients. Patients with HLH, however, cannot control the hyperinflammatory response which, if untreated, is fatal in genetic cases and in a high percentage of acquired cases. Awareness of the clinical symptoms and of the diagnostic criteria of HLH is important to start life-saving therapy with immunosuppressive/immunomodulatory agents in time.
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              Hemophagocytic lymphohistiocytosis: an update on diagnosis and pathogenesis.

              Hemophagocytic lymphohistiocytosis (HLH) is a frequently fatal and likely underdiagnosed disease involving a final common pathway of hypercytokinemia, which can result in end-organ damage and death. Although an early diagnosis is crucial to decrease mortality, the definitive diagnosis is often challenging because of the lack of specificity of currently accepted diagnostic criteria and the absence of confirmatory gold standards. Because of the wide range of laboratory assays involved in the diagnosis of HLH, practicing pathologists from a broad spectrum of clinical specialties need to be aware of the disease so that they may appropriately flag results and convey them to their clinical counterparts. Our article summarizes these new advances in the diagnosis of HLH and includes a review of clinical findings, updated understanding of the pathogenesis, and promising new testing methods.
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                Author and article information

                Journal
                Dis Markers
                Dis. Markers
                DM
                Disease Markers
                Hindawi Publishing Corporation
                0278-0240
                1875-8630
                2016
                27 March 2016
                : 2016
                : 1523959
                Affiliations
                1Department of Cardiology, Beijing University of Chinese Medicine Third Affiliated Hospital, Beijing 100029, China
                2Departments of Clinical Laboratory, Beijing Youan Hospital, Capital Medical University, Beijing 100069, China
                Author notes

                Academic Editor: Michele Malaguarnera

                Article
                10.1155/2016/1523959
                4826701
                27110054
                3c742a0e-d0a9-414a-9878-8aef333c0413
                Copyright © 2016 Tiantong Jiang et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 12 January 2016
                : 6 March 2016
                Categories
                Research Article

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