Disease | pancytopenia |
Symptom | C0019214|hepatosplenomegaly |
Sentences | 5 |
PubMedID- 25332523 | This case highlights the importance of considering hepatosplenic t cell lymphoma as differential diagnosis in the clinical setting of pancytopenia with hepatosplenomegaly to allow timely diagnosis of these aggressive neoplasms. |
PubMedID- 21919309 | Hemophagocytic syndrome (hps) features fever and hepatosplenomegaly associated with pancytopenia, hypertriglyceridemia, and hypofibrinogemia, due to hypercytokinemia. |
PubMedID- 21152410 | Hemophagocytic lymphohistiocytosis (hlh) is characterized by fever and hepatosplenomegaly associated with pancytopenia . |
PubMedID- 22736603 | Hlh, primary or secondary, is characterised by prolonged fever and hepatosplenomegaly associated with pancytopenia, hypertriglyceridaemia and hypofibrinogenaemia. |
PubMedID- 23467543 | The infection may involve multiple organ systems, including the gastrointestinal tract (with resulting ulceration), adrenal glands (precipitating adrenal insufficiency), the reticuloendothelial system (causing hepatosplenomegaly), bone marrow (leading to pancytopenia), the central nervous system, and the lungs. |
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