TAFRO syndrome (Q92905): Difference between revisions
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A síndrome TAFRO é um transtorno inflamatório sistêmico caracterizado por trombocitopenia, anasarca, incluindo derrame pleural e ascite, febre, insuficiência renal e organomegalia, incluindo hepatoesplenomegalia e linfadenopatia. Seu início pode ser agudo ou subagudo, mas sua etiologia é indeterminada. | |||
| description / en | description / en | ||
TAFRO syndrome is a systemic inflammatory disorder characterised by thrombocytopenia, anasarca including pleural effusion and ascites, fever, renal insufficiency, and organomegaly including hepatosplenomegaly and lymphadenopathy. Its onset may be acute or sub-acute, but its etiology is undetermined. | |||
Revision as of 08:01, 16 August 2026
TAFRO syndrome is a systemic inflammatory disorder characterised by thrombocytopenia, anasarca including pleural effusion and ascites, fever, renal insufficiency, and organomegaly including hepatosplenomegaly and lymphadenopathy. Its onset may be acute or sub-acute, but its etiology is undetermined.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1505841618 |
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| English | TAFRO syndrome |
TAFRO syndrome is a systemic inflammatory disorder characterised by thrombocytopenia, anasarca including pleural effusion and ascites, fever, renal insufficiency, and organomegaly including hepatosplenomegaly and lymphadenopathy. Its onset may be acute or sub-acute, but its etiology is undetermined. |
