Emphysematous pyelonephritis in patient with hemophagocytic lymphohistiocytosis: A case report

Autoimmune Lymphoproliferative Syndrome Misdiagnosed as Hemophagocytic Lymphohistiocytosis A Case Report

Autoimmune lymphoproliferative Syndrome (ALPS) is a rare inherited disorder of apoptosis. It usually presents with chronic lymphadenopathy, splenomegaly, and symptomatic cytopenia in a child. Herein, we report a 14-year-old boy with symptoms misdiagnosed as hemophagocytic lymphohistiocytosis who was treated before ALPS was diagnosed for the patient. This case should alert pediatricians to consi...

Emphysematous Pyelonephritis: A Case Report

hemophagocytic lymphohistiocytosis in a neonate: case report

hemophagocytic lymphohistiocytosis (hlh) is a syndrome of pathologic immune activation, occurring as either a familial disorder or a sporadic condition, in association with a variety of triggers. this article will introduce a neonate with hlh in iran. we report a case of hlh presenting with respiratory distress and fever, hepatosplenomegaly, jaundice and pancytopenia on the second day of life. ...

Neonatal hemophagocytic lymphohistiocytosis--case report.

Hemophagocytic lymphohystiocytosis (HLH) represents a severe hyperinflammatory condition with the cardinal symptoms prolonged fever, hepatosplenomegaly, and cytopenias. The most prominent histopathological feature of HLH is an accumulation of activated T lymphocytes and macrophages predominantly in lymphoid tissues. Although it can occur in all age groups, neonatal-onset HLH is very rare. We re...

Hemophagocytic Lymphohistiocytosis in a Neonate: Case Report.

 Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of pathologic immune activation, occurring as either a familial disorder or a sporadic condition, in association with a variety of triggers. This article will introduce a neonate with HLH in Iran. We report a case of HLH presenting with respiratory distress and fever, hepatosplenomegaly, jaundice and pancytopenia on the second day of life....