Hemophagocytic Lymphohistiocytosis in B-Cell Lymphoproliferative Disorder: Report of a Rare Association
✍ Scribed by Deepti Aggarwal; Ruchika Gupta; Sompal Singh; Kusum Gupta; Madhur Kudesia
- Book ID
- 107645370
- Publisher
- Springer-Verlag
- Year
- 2010
- Tongue
- English
- Weight
- 372 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0971-4502
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract ## Background Epstein‐Barr virus‐associated hemophagocytic lymphohistiocytosis (EBV‐HLH), also known as EBV‐associated hemophagocytic syndrome, develops mostly in children and young adults and may be fatal. Early etoposide treatment has been confirmed to be effective in children. Howev
Aplastic anemia is a disorder characterized by pancytopenia and bone marrow hypocellularity. There is some evidence that aplastic anemia may be due to suppression of hematopoiesis by activated T-suppressor cells. Thus, immunosuppressive agents have been used as an alternative to bone marrow transpla
## Abstract Lymphoproliferative disorder (LPD) is described in only a few children receiving chemotherapy for cancer. In all of them, an association between LPD and EBV (Epstein‐Barr Virus) was found. We report on a patient who developed LPD not associated with EBV while receiving chemotherapy for
## Abstract We report a case of an EBV‐associated high grade B‐cell lymphoproliferative disorder occurring in the synovial membrane of an elderly patient with gout arthropathy. The EBV‐infected B‐cells displayed a pattern of viral gene expression (EBNA2^+^/LMP1^+^) typically seen during primary EBV