Hemophagocytic syndrome.

Autor: Dhawale MS; Department of Pathology, Government Medical College and Hospital, C/O L.C. Deo 39, SBH Colony, Near Peer Bazaar, Osmanpura, Aurangabad, 431003 Maharashtra India., Joshi AR; Department of Pathology, Government Medical College and Hospital, C/O L.C. Deo 39, SBH Colony, Near Peer Bazaar, Osmanpura, Aurangabad, 431003 Maharashtra India., Bhatkule MA; Department of Pathology, Government Medical College and Hospital, C/O L.C. Deo 39, SBH Colony, Near Peer Bazaar, Osmanpura, Aurangabad, 431003 Maharashtra India., Kumbhakarna NR; Department of Pathology, Government Medical College and Hospital, C/O L.C. Deo 39, SBH Colony, Near Peer Bazaar, Osmanpura, Aurangabad, 431003 Maharashtra India., Bindu RS; Department of Pathology, Government Medical College and Hospital, C/O L.C. Deo 39, SBH Colony, Near Peer Bazaar, Osmanpura, Aurangabad, 431003 Maharashtra India.
Jazyk: angličtina
Zdroj: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion [Indian J Hematol Blood Transfus] 2014 Sep; Vol. 30 (Suppl 1), pp. 9-11. Date of Electronic Publication: 2012 Dec 18.
DOI: 10.1007/s12288-012-0217-0
Abstrakt: Hemophagocytic syndrome is a life threatening condition characterized by uncontrolled hyperinflammation on the basis of various inherited or acquired immune deficiencies. We report a case of hemophagocytic syndrome in a 18 years old male with a brief review of literature.
Databáze: MEDLINE
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