منابع مشابه
MR Findings of Fulminent Leukoencephalopathy in EBV-Associated Hemophagocytic Syndrome
Various manifestations of brain involvement for patients with virus-associated hemophagocytic syndrome have been reported. Here, we report on the sequential magnetic resonance (MR) findings of acute demyelination of the entire brain with subsequent brain atrophy in a follow-up study of a 25-month- old boy who was admitted with fever and then diagnosed with infectious mononucleosis and EBV-assoc...
متن کاملEBV associated hemophagocytic lymphohistiocytosis with spontaneous regression.
INDIAN PEDIATRICS 1253 VOLUME 42DECEMBER 17, 2005 A 9-year-old boy, previously healthy, was referred to our center with 10 days of fever, weakness, epistaxis and purpura. Examination revealed a febrile child who had marked pallor; petechiae over limbs and trunk; 1-1.5 cm multiple sub-mental lymph nodes; 3 cm hepatomegaly and 5 cm splenomegaly below costal margins respectively. Investigations (T...
متن کاملInfection-associated Hemophagocytic Syndrome
An epidemic of an infection associated with circulating hemophagocytes (HP) and activated monocytes (AM) was seen in Bombay. Although certain features overlapped with the well-defined entity of virus-associated hemophagocytic syndrome and familial hemophagocytic lymphohistiocytosis, it was distinct enough to place it in a separate category. Affected children were predominantly two days to two y...
متن کاملMumps Virus–associated Hemophagocytic Syndrome
To the Editor: Virus-associated hemophagocytic syndrome (VAHS) is a fulminant disorder associated with systemic viral infection and is characterized pathologically by the proliferation of hemophagocytic histiocytes in the lymphoreticular tissues. Here we report a case of mumps VAHS following parotitis and pancreatitis. A 39-year-old, previously healthy woman sought treatment for abdominal pain ...
متن کاملAutoimmune-Associated Hemophagocytic Syndrome/Macrophage Activation Syndrome
Hemophagocytic syndrome (HPS), also known as hemophagocytic lymphohistiocytosis (HLH) encompasses an infrequent group of non-malignant, yet potentially life-threatening disorders caused by massive cytokine release from activated lymphocytes and macrophages (Filipovich, 2009; Henter et al., 1998, 2007; Janka et al., 1998; Janka, 2009). This multisystem inflammatory syndrome is associated with a ...
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ژورنال
عنوان ژورنال: American Journal of Hematology
سال: 2011
ISSN: 0361-8609
DOI: 10.1002/ajh.21811