Author/Authors
Solmaz, Soner Başkent University Adana Hospital - Department of Hematology, Turkey , Boğa, Can Başkent University Adana Hospital - Department of Hematology, Turkey , Kozanoğlu, İlknur Başkent University Adana Hospital - Department of Hematology, Turkey , Asma, Süheyl Başkent University Adana Hospital - Department of Hematology, Turkey , Turunç, Tuba Başkent University Adana Hospital - Department of Infectious Diseases, Turkey , Demiroğlu, Yusuf Ziya Başkent University Adana Hospital - Department of Infectious Diseases, Turkey
Title Of Article
A rare hematological complication of visceral leishmaniasis: hemophagocytic syndrome
شماره ركورد
24157
Abstract
The term “hemophagocytosis” describes the pathologic finding of activated macrophages, engulfing erythrocytes, leukocytes, platelets and their precursor cells. This phenomenon is an important finding in patients with hemophagocytic syndrome. It is a distinct clinical entity characterized by fever, pancytopenia, splenomegaly and hemophagocytosis in bone marrow, liver and lymph nodes. Hemophagocytic syndrome can be classified according to the underlying etiology into either primary (genetic) or secondary (acquired). Severe infections, malignancies, rheumatologic disorders and some metabolic diseases can lead to secondary hemophagocytic syndrome. Infection-associated hemophagocytic syndrome implicating Leishmania is very rare and often difficult to diagnose. Therefore, we aimed to report a young boy with Visceral Leishmaniasis associated hemophagocytic syndrome.
From Page
161
NaturalLanguageKeyword
Leishmania , hemophagocytic syndrome , hemophagocytosis , zoonoses
JournalTitle
Cukurova Medical Journal
To Page
163
JournalTitle
Cukurova Medical Journal
Link To Document