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

Yıl 2021, Cilt: 11 Sayı: 4, 582 - 585, 31.07.2021

Deniz İncaman

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

Öz

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.

Anahtar Kelimeler

Hemophagocytic syndrome , jaundice , pancytopenia

Proje Numarası

yok

Hemofagositik sendrom, erken tanıya rağmen mortal seyreden bir olgu

Öz

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.

Anahtar Kelimeler

hemafagositik sendrom , ikter , pansitopeni

Destekleyen Kurum

yok

Proje Numarası

yok

Kaynakça

• 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.