ABSTRACT

Hemophagocytic histiocytosis is a syndrome of similar inflammatory response that can occur with different underlying pathologies that can be seen at any age. It is a rare disease characterized by fever, splenomegaly, jaundice, hemophagocytosis of bone marrow and other tissues (phagocytosis of erythrocytes, leukocytes platelets and their precursors by macrophages). There are two forms as primary and secondary, primary form (familial hemophagocytic syndrome) is autosomal recessive inheritance. It is seen in newborn children approximately 1/50.000 ratios. The secondary form is especially associated with Epstein-Barr virus infection, but it can be seen together with viral, bacterial, fungal and parasitic infections, collagen tissue diseases and malignant diseases. In this article, a 44-year-old female patient with no chronic disease history and has respiratory complaints was admitted to the chest diseases service with pre-diagnosis of pneumonia and the patient was admitted to the intensive care unit after the development of acute respiratory distress syndrome (ARDS). In this case, the development of hemophagocytic syndrome due to ARDS which is rarely seen syndrome is presented while ARDS therapy continues.

Keywords: Acute respiratory distress syndrome, hemophagocytic syndrome, intensive care