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Felty's syndrome

disorder
SNOMED 57160007CUI C0015773

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Research Evidence

Peer-reviewed studies linked via MeSH term "Felty Syndrome" from the MEDLINE/PubMed database.

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The spectrum of somatic mutations in large granular lymphocyte leukemia, rheumatoid arthritis, and Felty's syndrome.
[object Object], [object Object], [object Object] · Semin Hematol · 2022
PMID: 36115688Review
Hematological Manifestations among Patients with Rheumatic Diseases.
[object Object], [object Object] · Acta Haematol · 2021
PMID: 33221805Review
Chronic neutropenia in LGL leukemia and rheumatoid arthritis.
[object Object], [object Object] · Hematology Am Soc Hematol Educ Program · 2017
PMID: 29222254ReviewFull text (PMC)
Treatment of pseudo Felty's syndrome: Is there a place for rituximab?
[object Object], [object Object], [object Object] et al. · Joint Bone Spine · 2015
PMID: 25623522Review
Citrullination of autoantigens implicates NETosis in the induction of autoimmunity.
[object Object], [object Object] · Ann Rheum Dis · 2014
PMID: 24291655Review
[Large granular lymphocyte leukemia: clinical and pathogenic aspects].
[object Object], [object Object], [object Object] et al. · Rev Med Interne · 2013
PMID: 23928096Review
Autoimmune manifestations in large granular lymphocyte leukemia.
[object Object], [object Object] · Clin Lymphoma Myeloma Leuk · 2012
PMID: 22999943Review
Neutrophil activation and B-cell stimulation in the pathogenesis of Felty's syndrome.
[object Object], [object Object] · Pol Arch Med Wewn · 2012
PMID: 22814518Review
Gastrointestinal and hepatic manifestations of rheumatoid arthritis.
[object Object], [object Object] · Dig Dis Sci · 2011
PMID: 21203902Review
Search all PubMed articles for Felty's syndrome

Research data from MEDLINE/PubMed

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Arthralgias
Very frequent (80-99%)HP:0002829
Arthritis
Very frequent (80-99%)HP:0001369
Autoimmunity
Very frequent (80-99%)HP:0002960
Breakdown of bone
Very frequent (80-99%)HP:0002797
Immune deficiency
Very frequent (80-99%)HP:0002721
Joint disease
Very frequent (80-99%)HP:0001367
Limitation of joint mobility
Very frequent (80-99%)HP:0001376
Multiple, subcutaneous nodules
Very frequent (80-99%)HP:0001482
Neutropoenia
Very frequent (80-99%)HP:0001875
Predisposition to infections
Very frequent (80-99%)HP:0002719
respiratory infections, recurrent
Very frequent (80-99%)HP:0002205
Synovitis
Very frequent (80-99%)HP:0100769
Abnormal lymphocytes
Frequent (30-79%)HP:0004332
Chronic middle ear infection
Frequent (30-79%)HP:0000389
Decreased haemoglobin
Frequent (30-79%)HP:0001903
Large spleen
Frequent (30-79%)HP:0001744
Lymph node hyperplasia
Frequent (30-79%)HP:0002716
Nasal inflammation
Frequent (30-79%)HP:0012384
Pneumonia, recurrent
Frequent (30-79%)HP:0006532
Recurrent sore throat
Frequent (30-79%)HP:0100776
Sinusitis
Frequent (30-79%)HP:0000246
Weight loss
Frequent (30-79%)HP:0001824
Bacterial infection of skin
Occasional (5-29%)HP:0100658
Cancer of lymphatic system
Occasional (5-29%)HP:0002665
Enlarged liver
Occasional (5-29%)HP:0002240
Episcleritis
Occasional (5-29%)HP:0100534
Generalised hyperpigmentation
Occasional (5-29%)HP:0007440
Hypoplastic bone marrow
Occasional (5-29%)HP:0005528
Infection in blood stream
Occasional (5-29%)HP:0100806
Irregular hyperpigmentation
Occasional (5-29%)HP:0007400

Quick Facts

SNOMED CT
57160007
UMLS CUI
C0015773
Fully Specified Name
Felty's syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
30
Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.