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Artikel ; Online: Hemophagocytic lymphohistiocytosis

Brittany Grzybowski / Vijay A Vishwanath

Journal of Pediatric Neurosciences, Vol 12, Iss 1, Pp 55-

A diagnostic conundrum

2017  Band 60

Abstract: Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of excessive immune activation causing widespread inflammation and tissue destruction leading to multi-organ dysfunction and failure. Making the diagnosis of HLH could be quite challenging due to the ...

Abstract Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of excessive immune activation causing widespread inflammation and tissue destruction leading to multi-organ dysfunction and failure. Making the diagnosis of HLH could be quite challenging due to the broad range of presenting symptoms and their lack of specificity. After ruling out considerations for differential diagnoses, recognizing the most common presenting signs and symptoms of HLH, including neurologic dysfunction, and having a high clinical suspicion for HLH in the setting of inflammatory/demyelinating diseases are important for prompt diagnosis and treatment.
Schlagwörter Acute disseminated encephalomyelitis ; encephalopathy ; familial hemophagocytic lymphohistiocytosis ; hemophagocytic lymphohistiocytosis ; seizures ; Pediatrics ; RJ1-570 ; Medicine ; R ; Neurosciences. Biological psychiatry. Neuropsychiatry ; RC321-571 ; Internal medicine ; RC31-1245
Sprache Englisch
Erscheinungsdatum 2017-01-01T00:00:00Z
Verlag Medknow Publications
Dokumenttyp Artikel ; Online
Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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