Case Series of Hemophagocytic Lymphohistiocytosis from a Tertiary Care Centre: An Underdiagnosed Entity
Objective: Hemophagocytic Lymphohistiocytosis (HLH) is an uncommon, life-threatening hyperinflammatory syndrome, caused by severe hypercytokinemia, due to an overstimulated but ineffective immune process. The presenting features of HLH are non-specific, mimicking many other diseases, and hence its e...
Main Authors: | Vijay KUMAR, Bhavna SHARMA, Abhay S. NIGAM |
---|---|
Format: | Article |
Language: | English |
Published: |
Federation of Turkish Pathology Societies
2019-09-01
|
Series: | Türk Patoloji Dergisi |
Subjects: | |
Online Access: |
http://www.turkjpath.org/pdf.php3?id=1893
|
Similar Items
-
Measles and Secondary Hemophagocytic Lymphohistiocytosis
by: Julien Lupo, et al.
Published: (2012-09-01) -
Infection associated hemophagocytic lymphohistiocytosis: An institutional experience
by: Kavitha Kanjirakkattumana Parameswaran, et al.
Published: (2019-07-01) -
Hemophagocytic lymphohistiocytosis: Uncommon systemic inflammatory clinical syndrome
by: Paparao N, et al.
Published: (2016-09-01) -
Germline Compound Heterozygous Variants Identified in the STXBP2 Gene Leading to a Familial Hemophagocytic Lymphohistiocytosis Type 5: A Case Report
by: Vera Maria Dantas, et al.
Published: (2021-06-01) -
Brucellosis presenting with pancytopenia due to hemophagocytic syndrome
by: Ela Erdem, et al.
Published: (2011-03-01)