TY  - JOUR
T1  - Hemophagocytic Syndrome; A Mortal Progressing Case Despite Early Diagnosis and Treatment
TT  - Hemofagositik sendrom, erken tanıya rağmen mortal seyreden bir olgu
AU  - İncaman, Deniz
PY  - 2021
DA  - July
Y2  - 2021
DO  - 10.16899/jcm.944765
JF  - Journal of Contemporary Medicine
JO  - J Contemp Med
PB  - Rabia YILMAZ
WT  - DergiPark
SN  - 2667-7180
SP  - 582
EP  - 585
VL  - 11
IS  - 4
LA  - en
AB  - 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.
KW  - Hemophagocytic syndrome
KW  - jaundice
KW  - pancytopenia
N2  - 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.
CR  - 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.
UR  - https://doi.org/10.16899/jcm.944765
L1  - https://dergipark.org.tr/en/download/article-file/1795076
ER  -