MEDITERRANEAN JOURNAL OF HEMATOLOGY AND INFECTIOUS DISEASES www.mjhid.org ISSN 2035-3006 Case Reports Epstein-Barr Virus (EBV)-Associated Associated Haemophagocytic Syndrome

We describe the case of a 17 syndrome (HPS) one month following acute infection caused by Epstein initiation of treatment and reduction of EBV load, laboratory signs of HPS as severe cytopenia, hypofibrinogenemia, hyperferritinemia and hypertriglyceridemia p multiorgan failure. HPS is a rare, but life Introduction. The haemophagocytic syndrome (HPS) represents a severe and aggressive hyperinflammatory disease with major diagnostic and therapeutic difficulties. HPS is a spectrum of inherited and acquired conditions with disturbed immune regulation which results into a dysregulated ac proliferation of lymphocytes. Haemophagocytosis is part of a sepsis-like syndrome caused by severe hypercytokinemia as result of a highly stimulated but ineffective immune response. Cardinal symptoms are prolonged fever, cytopenia affecting a three lineages, hepatosplenomegaly and coagulopathy with hypofibrinogenemia. Diagnostic criteria for this disorder are shown in Table 1 edited by the Histiocyte Society. HPS may be the consequence of a familial immune dysregulatory disorder or be associated with a number of different infections, autoimmune disorders or malignancies, like lymphomas or carcinomas Frequent triggers are infectious agents, especially virus of the herpes group. Among the infectious agents www.mjhid.org ISSN 2035-3006 Haemophagocytic Syndrome , Annarosa Cuccaro, Elena Maiolo , Stefan Hohaus and Luciana Teofili , Microbiology and Anaesthesiology, Catholic University, Rome, Italy , Catholic University of Rome -6-3055153. E-mail: lteofili@rm.unicatt.it at no competing interests exist. 2, 4(1): e2012008, DOI: 10.4084/MJHID.2012.008 Creative Commons Attribution License ), which permits unrestricted use, distribution, and reproduction in any medium, . year old female who developed fatal haemophagocytic -Barr virus (EBV). Despite ersisted, and the patient died of -threatening complication of EBV infection.

We describe the case of a 17-year old female who developed fatal haemophagocytic syndrome (HPS) one month following acute infection caused by Epstein-Barr virus (EBV). Despite initiation of treatment and reduction of EBV load, laboratory signs of HPS as severe cytopenia, hypofibrinogenemia, hyperferritinemia and hypertriglyceridemia persisted, and the patient died of multiorgan failure. HPS is a rare, but life-threatening complication of EBV infection. syndrome (HPS) represents a severe and aggressive hyperinflammatory disease with major diagnostic and therapeutic HPS is a spectrum of inherited and acquired conditions with disturbed immune regulation which results into a dysregulated activation and proliferation of lymphocytes. Haemophagocytosis is like syndrome caused by severe hypercytokinemia as result of a highly stimulated but ineffective immune response. Cardinal symptoms are prolonged fever, cytopenia affecting at least two of three lineages, hepatosplenomegaly and coagulopathy with hypofibrinogenemia. Diagnostic criteria for this edited by the Histiocyte HPS may be the consequence of a familial immune er or be associated with a number of different infections, autoimmune disorders or malignancies, like lymphomas or carcinomas. 4 EBV-associated haemophagocytic syndrome has a relatively high incidence in Asian countries and particularly in Japan. 3 Here we present a case of EBV associated haemophagocytic syndrome in a young Italian women that was fatal despite prompt medical treatment.

Case Presentation.
A 17 year admitted to our hospital for fever, fatigue and abdominal discomfort. Her medical history showed no relevant data; in particular no recurrent infectious episodes were documented except for the common childhood diseases. One month before the admission, the patient suffered from infectious mononucleosis. She had developed a widespread skin rash during antibiotic therapy with amoxicillin given for fever. Here we present a case of EBVassociated haemophagocytic syndrome in a young Italian women that was fatal despite prompt medical A 17 year-old white woman was ur hospital for fever, fatigue and

Haemophagocytic Syndrome
Her medical history showed no relevant data; in particular no recurrent infectious episodes were documented except for the common One month before the admission, the patient suffered from infectious mononucleosis. She had developed a widespread skin rash during antibiotic therapy with amoxicillin given for fever. A Table 1: Diagnostic criteria for HPS: One of two criteria should be present for correct diagnosis 4 1) Molecular diagnosis of familial haemophagocytosis (Pathologic mutations of Perforin (PRF1), SH2D1A/SAP, UNC13D, Syntaxin 11 (STX11), MUNC18-2, Ras-related Protein Rab27a (RAB27a)) Or 2) Five out of eight diagnostic criteria listed below are fulfilled: 1. Fever ≥38.5°C 2. Splenomegaly 3. Cytopenias (affecting at least 2 of 3 lineages in the peripheral blood): Hemoglobin <9 g/dl (in infants <4 weeks: hemoglobin <10 g/dl) Platelets <100X103/ml Neutrophils <1X103/ml 4. Hypertriglyceridemia (fasting, > 265 mg/dl) and/or hypofibrinogenemia (<150 mg/dl) 5. Hemophagocytosis in bone marrow or spleen or lymph nodes or liver 6. Low or absent NK-cell activity 7. Ferritin > 500 ng/ml 8. Elevated Soluble CD25 (alpha chain of soluble IL-2 receptor) that time, the monospot test resulted positive and the patient received corticosteroids with symptoms improvement. On admission, the physical examination showed splenomegaly without palpable lymphadenopathy. Laboratory evaluation revealed a severe pancytopenia: platelet count was 17x 10 6 /mmc, hemoglobin was 7,2 g/dl and she had a leucocyte count of 230/mmc. Lactate dehydrogenase was strongly increased to 1570 UI/l, while GPT was 217 U/l and bilirubin was Serological studies for HIV 1,2, hepatitis B and C, cytomegalovirus, parvovirus were negative. Both IgG and IgM anti-viral capsid antigen (VCA) EBV antibodies were positive, while anti-EBV nuclear antigen were negative, indicating a recent primary EBV infection. Amplification of EBV-DNA from whole blood by polymerase chain reaction (PCR) yielded 930.000 copies/ml. As the patient presented signs of an acute colecystitis, she was treated with trans-hepatic drainage of the gall-bladder. Acute acalcolous colecystitis (AAC) observed in our patient, reflected the severe inflammatory response associated with the primary EBV infection.
In addition, the bile stasis can also been implicated in the gallbladder inflammation pathogenesis. Moreover, also EBV-induced hepatitis has been recognized as an important cause of cholestasis. Finally, another possible pathogenetic mechanism, may be the direct invasion of the gallbladder from the EBV-virus. AAC may develop during the course of acute EBV infection, especially in patients with cholestatic hepatitis. 6,7 Clinical conditions of our patient rapidly deteriorated and she was transferred to the  intensive care unit on day 2 following admission. Hemophagocytic syndrome was suspected and confirmed by a second bone marrow examination ( Table 3). Bone marrow cytology and histology revealed several histiocytes with phagocytosis of erythrocytes and platelets (Figure 1). The bone marrow biopsy showed phagocytic cells with engulfed haemopoietic elements. The presence of large sized T lymphocytes in the biopsy raised the suspicion of EBV-related T-lymphoproliferative disease.
The patient was immediately started on high doses of corticosteroids and immunoglobulins (1g/kg for two days). As the clinical conditions did not improve, treatment with etoposide was started according to the HLH-94 protocol. Etoposide was administered in a dose of 150 mg/m 2 , on day 9 and day 12. EBV copy numbers slowly decreased, and laboratory signs of HPS as severe hypofibrinogenemia and hyperferrtinemia improved ( Figure  2), but pancytopenia persisted and the patient was supported with massive transfusions of blood and fresh frozen plasma, granulocyte-colony stimulating factor (G-CSF), and antibiotics. The patient died in multiorgan failure on day 15 following admission.

Discussion.
Haemophagocytic syndrome (HPS) is the most severe complication of infectious mononucleosis. HPS is a highly fatal disease if untreated or treated late. Diagnosing HPS is a challenge, as there is no single simple diagnostic test, and it remains a syndromic disorder with a combination of typical findings being often initially absent but developing with progressive disease. Because of diagnostic difficulties, diagnosis of HPS is often delayed and only established when the patient is already critically ill and transferred to the intensive care unit, as in our case.
As EBV responds poorly to antiviral agents, treatment is aimed at controlling the lymphocyte/macrophage activation and proliferation.
In addition to corticosteroids and immunoglobulins, treatment of EBV-associated HPS often requires administration of etoposide. 8,9 Repetitive administration of a myelosuppressive agent in an already severe cytopenic patient with a high risk for additional infectious complications is not trivial, and should be limited to centers experienced in treatment of acute haematological diseases.
Since HPS is rare, no data are available from randomized controlled clinical trials testing potential different treatment approaches. As T cell dysregulation appears to be involved in the pathogenesis of both primary and secondary HPS, treatment with antithymocyte globulins (ATG) has been reported as an alternative to etoposide-based therapy in a single center study on patients with familial HPS. 10 An on-going trial of the Histiocyte Society studies the early addition of cyclosporine to the etoposide-based regimen. 11 An additional therapy for patients with progressive EBVassociated HPS may be rituximab, at it can eliminate EBV-infected B cells. 12 Bone marrow histology raised the suspicion of a T cell lymphoma in our patient. Lymphomas of T-cell and NK-cell origin are among the most common neoplasias associated with secondary malignancyassociated HPS. 4,5,11 This association has been more frequently been reported in Asian countries where the incidence of EBV-associated lymphomas appear to be significantly higher. In fact some studies describe fulminant EBV-T cell lymphoproliferative disorders following acute EBV-infection. 13 However, the suspicion in our patient was not substantiated by other signs of a lymphoproliferative disease, although we cannot rule out that the EBV-induced lymphoproliferation in our patient was already indication of transformation into a malignant disease. lymphoma.
In conclusion, our case highlights that hemophagocytic syndrome can complicate acute EBV-infection, and should raise the awareness for this rare life-threatening syndrome in order to promptly start appropriate treatment.