Dergiler / Journal of Contemporary Medicine / 2021 / Cilt: 11 - Sayı: 4

Hemofagositik sendrom, erken tanıya rağmen mortal seyreden bir olgu

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

Sayfa
582–585
DOI
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Özet

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.

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.

Anahtar kelimeler: hemafagositik sendrom, ikter, pansitopeni