Serum ferritin and lactate dehydrogenase in a case of hemophagocytic lymphohistiocytosis.
نویسندگان
چکیده
A 40-day-old baby girl presented with intermittent fever, lymphadenopathy, massive hepatosplenomegaly, progressive pancytopenia and features of disseminated intravascular coagulopathy. A bone marrow aspiration was performed and showed florid histiocytic proliferation with marked hemophagocytosis. Based on the diagnostic guideline for Hemophagocytic Lymphohistiocytosis proposed by the Familial Hemophagocytic Lymphohistiocytosis Study Group of Histiocyte Society, this patient has fulfilled most of the criteria. We have also found that serum ferritin and lactate dehydrogenase to be very high in this patient. It remains uncertain whether the disorder is reactive or neoplastic.
منابع مشابه
Hemophagocytic lymphohistiocytosis prior to the diagnosis of Kawasaki disease.
A 9-year-old girl was hospitalized on 7th day of illness because of prolonged fever and cervical lymphadenopathy. On admission, leukopenia (total leukocyte count 1.1×109/L) and thrombocytopenia (platelet count 60×109/L) were present. Serum aspartate aminotransferase (128 U/L), alanine aminotransferase (99 U/ L), lactate dehydrogenase (518 U/L), ferritin (823 mg/ dL), soluble interleukin-2 recep...
متن کاملSecondary hemophagocytic lymphohistiocytosis possibly induced by interferon beta-1a therapy.
A 57-year old woman with a history of multiple sclerosis, treated with interferon beta-1a in the last 5 months, was referred for hyperpyrexia (>40°C) that persisted for 15 days. At admission, there was elevation of transaminases, anemia (hemoglobin 8.9 g/dL), thrombocytopenia (platelet 135,000/mm3), and hypofibrinogenemia (fibrinogen 1.26 g/L). C-reactive protein was 10.7 mg/dL, lactate dehy...
متن کاملSoluble interleukin-2 receptor: a useful prognostic factor for patients with hemophagocytic lymphohistiocytosis.
Elevation of serum concentrations of soluble interleukin-2 receptor (sIL-2R) has been shown in various hematolymphoid malignancies.'" Since its first documentation by Komp et alx in 1989, sIL2R has also been measured and tested for clinical usefulness as a prognostic indicator for patients with hemophagocytic lymphohistiocytosis (HLH)?"' However, these studies evaluated a small number of patien...
متن کاملIntense myelofibrosis in a child: unusual result of EBV-associated hemophagocytic lymphohistiocytosis.
A previously healthy 12-year-old girl was admitted to the intensive care unit with severe pulmonary bleeding. Her history revealed that she had suffered from high fever, fatigue, sore throat, myalgia and generalized rash for two weeks. Physical examination revealed hepatosplenomegaly. Laboratory investigation showed pancytopenia associated with unusual high levels of serum ferritin, triglycerid...
متن کاملT Cell Histiocyte Rich Large B Cell Lymphoma Presenting as Hemophagocytic Lymphohistiocytosis: An Uncommon Presentation of a Rare Disease
T cell histiocyte rich large B cell lymphoma (THRLBCL) is a rare subtype of non-Hodgkin's lymphoma characterized by malignant B cells with reactive T lymphocytes. The pathophysiology is thought to involve cytokine-mediated evasion of T cell immune response by malignant B cells. It usually presents at an advanced stage with extranodal involvement. An extremely unusual manifestation of the diseas...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The Malaysian journal of pathology
دوره 20 2 شماره
صفحات -
تاریخ انتشار 1998