Familial haemophagocytic lymphohistiocytosis (Q88710): Difference between revisions
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Linfohistiocitose hemofagocítica familiar (LHF) é caracterizada por uma síndrome de ativação macrofágica que se apresenta com febre alta inexplicada, irritabilidade, dor generalizada, edema e hepatoesplenomegalia, ocorrendo usualmente após um período assintomático que pode durar de vários meses até, mais raramente, vários anos após o nascimento. | |||
| description / en | description / en | ||
Familial hemophagocytic lymphohistiocytosis (FHL) is characterised by a macrophage activation syndrome presenting with unexplained high fever, irritability, general pain, oedema and hepatosplenomegaly, usually occurring after a healthy period that may range from several months after the birth to, more rarely, several years. | |||
Revision as of 15:05, 15 August 2026
Familial hemophagocytic lymphohistiocytosis (FHL) is characterised by a macrophage activation syndrome presenting with unexplained high fever, irritability, general pain, oedema and hepatosplenomegaly, usually occurring after a healthy period that may range from several months after the birth to, more rarely, several years.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_950019605 |
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| English | Familial haemophagocytic lymphohistiocytosis |
Familial hemophagocytic lymphohistiocytosis (FHL) is characterised by a macrophage activation syndrome presenting with unexplained high fever, irritability, general pain, oedema and hepatosplenomegaly, usually occurring after a healthy period that may range from several months after the birth to, more rarely, several years. |
