Hemophagocytic Syndrome; A Mortal Progressing Case Despite Early Diagnosis and Treatment

Year 2021, Volume: 11 Issue: 4, 582 - 585, 31.07.2021

Deniz İncaman

https://doi.org/10.16899/jcm.944765

Abstract

In this case we discussed with a hemaphagocytic syndrome in a patient who was investigated for jaundice. Hemophagocytic syndrome; fever, hypertriglyceridemia, hepatosplenomegaly, bone marrow involvement is a multisystemic disease.This is due to excess cytokines released from the cells.Hemophagocytic syndrome, can occur as a familial or sporadic disorder, and it can be triggered by a variety of events that disrupt immune homeostasis.

Keywords

Hemophagocytic syndrome, jaundice, pancytopenia

Project Number

yok

Hemofagositik sendrom, erken tanıya rağmen mortal seyreden bir olgu

Abstract

In this case we discussed with a hemaphagocytic syndrome in a patient who was investigated for jaundice. Hemophagocytic syndrome; fever, hypertriglyceridemia, hepatosplenomegaly, bone marrow involvement is a multisystemic disease.This is due to excess cytokines released from the cells.Hemophagocytic syndrome, can occur as a familial or sporadic disorder, and it can be triggered by a variety of events that disrupt immune homeostasis.

Keywords

hemafagositik sendrom, ikter, pansitopeni

Supporting Institution

yok

Project Number

yok

References

• Rederans1 How I treat hemophagocytic lymphohistiocytosis. Jordan MB, Allen CE, Weitzman S, Filipovich AH, McClain KL, Blood. 2011;118(15):4041. Epub 2011 Aug 9. Referans2 The unique aspects of presentation and diagnosis of hemophagocytic lymphohistiocytosis in adults.Nikiforow S, Berliner N. Hematology Am Soc Hematol Educ Program. 2015;2015:183-9.