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1.
Indian Pediatr ; 2016 June; 53(6): 534
Artículo en Inglés | IMSEAR | ID: sea-179101
2.
Indian Pediatr ; 2016 Jun; 53(6): 505-511
Artículo en Inglés | IMSEAR | ID: sea-179055

RESUMEN

Hemophagocytic lymphohistiocytosis (HLH) is a multisystem disorder mediated by cytokine storm and is characterized by fever, pancytopenia and organomegaly coupled with laboratory features like hyperferritinemia, hypertriglyceridemia, hypofibrinogenemia and transaminitis. Etiology can be genetic or acquired such as infections, malignancy and autoimmune disorders. Diagnosis, identification of underlying etiology and management of HLH remain tough clinical puzzles to sort out for the managing physician. We report a clinico-pathological conference of a three-year-old boy who had such a presentation and succumbed during the hospital stay.

3.
Indian Pediatr ; 2015 July; 52(7): 601-606
Artículo en Inglés | IMSEAR | ID: sea-171702
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