Rheumatoid arthritis with splenomegaly and leukopenia (Q64192): Difference between revisions

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A tríade de artrite reumatoide (AR), esplenomegalia e neutropenia é chamada de síndrome de Felty. Neutropenia persistente (<2000 / mm3) deve estar presente, mas a tríade completa não é necessária para um diagnóstico de síndrome de Felty porque os pacientes sem esplenomegalia se assemelham aos pacientes com síndrome de Felty completa na maioria das características clínicas, sorológicas e imunogenéticas.
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The triad of rheumatoid arthritis (RA), splenomegaly, and neutropaenia is called Felty's syndrome. Persistent neutropaenia (<2000/mm3) must be present, but the complete triad is not required for a diagnosis of Felty's syndrome because patients without splenomegaly resemble patients with full-blown Felty's syndrome in most clinical, serologic, and immunogenetic features.
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Property / Canonical URI: https://id.who.int/icd/entity/1118910093 / rank
 
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CID11:ID_1118910093
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dki-india-ID_1118910093
Property / Canary Token: dki-india-ID_1118910093 / rank
 
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Concluído
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
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CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 11:46, 14 August 2026

The triad of rheumatoid arthritis (RA), splenomegaly, and neutropaenia is called Felty's syndrome. Persistent neutropaenia (<2000/mm3) must be present, but the complete triad is not required for a diagnosis of Felty's syndrome because patients without splenomegaly resemble patients with full-blown Felty's syndrome in most clinical, serologic, and immunogenetic features.
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    Rheumatoid arthritis with splenomegaly and leukopenia
    The triad of rheumatoid arthritis (RA), splenomegaly, and neutropaenia is called Felty's syndrome. Persistent neutropaenia (<2000/mm3) must be present, but the complete triad is not required for a diagnosis of Felty's syndrome because patients without splenomegaly resemble patients with full-blown Felty's syndrome in most clinical, serologic, and immunogenetic features.

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      CID11:ID_1118910093
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      dki-india-ID_1118910093
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      Concluído
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      13 August 2026
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