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Felty () described five patients with chronic some cases of Felty’s syndrome (Calabresi, Edwards, .. No se lleg6 a controlar la enfermedad por transfu. La enfermedad pulmonar intersticial (EPI) constituye Palabras clave: Enfermedad pulmonar intersticial, artritis reumatoide, tratamiento. . Síndrome de Felty. El síndrome de Felty se caracteriza por reunir la tríada compuesta por: artritis reumatoide, neutropenia y esplenomegalia. Es una enfermedad autoinmune poco.

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At least some cases of Felty syndrome are thought to be genetically determined. Felty syndrome is usually described as associated with or a complication of rheumatoid arthritis.

Create a personal account to register for email alerts with links to free full-text articles. Serious infection within the 3 months prior to randomization? Secondary anemia was present in all but one case, and in two patients low grade fever was detected.

Cancer AND drug name. Ishikawa K, Tsukada y, Tamura S, et al. Subjects will return to their normal standard of care therapy as determined wnfermedad their physician. Congenital and acquired neutropenia. Breastfeeding or nursing lactating women. The Merck Dw, 17th ed. Efermedad to search [pdf]. Create a free personal account to access your subscriptions, sign up for alerts, and more. Arch Intern Med Chic. In some affected individuals, Felty syndrome may develop during a period when the symptoms and physical findings associated with rheumatoid arthritis have subsided or are not present.


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Trials with results Trials without results. Pneumonia AND sponsor name. About News Events Contact. EU Clinical Trials Register. Diagnosis Felty syndrome is usually diagnosed as a result of a thorough clinical evaluation, a detailed patient history, and the identification of the classic triad of physical findings i.

Active psoriatic arthritis PsA defined as the presence of at least 3 tender and at least 3 swollen joints? End of the study is the date of ee last visit or the last scheduled procedure for the last active subject in the study whichever is later.

Males have one X and one Y chromosome and females have two X chromosomes. It is believed to be an autoimmune disorder that may be genetically transmitted as an autosomal dominant trait.


In this case, Felty syndrome may remain undiagnosed. Definition of the end of the trial and justification where it is not the last visit of the last subject undergoing the trial.

Merck Research Laboratories; Get free access to newly published articles. Trials with results Trials without results Clear advanced search filters. General Discussion Felty syndrome is usually described as associated with or a complication of rheumatoid arthritis. Combination product that includes a device, but does not involve an Advanced Therapy. Purchase access Subscribe to JN Learning for one year.


As a result of neutropenia, affected individuals are increasingly susceptible to certain infections. Some studies of families with Felty syndrome across several generations lead clinical geneticists enffrmedad suggest that a spontaneous mutation may occur that is transmitted as an autosomal dominant trait.

Evidence of active inflammatory arthritic syndromes or spondyloarthropathies other than PsA? Years Published, The numbered bands specify the location of the thousands of genes that are present on each chromosome. Sign in to customize your interests Sign in to your personal account. Presence of active psoriatic skin lesion or a history of plaque psoriasis Ps?

Serious disorder or illness other than psoriatic arthritis? Men must agree to use a reliable method of birth control or remain abstinent during the study? InFelty 1 described the occurrence in five middle-aged adults of a syndrome characterized by chronic deforming arthritis, splenomegaly, lymphadenopathy, leukopenia and cutaneous pigmentation. The exact cause of Felty syndrome is unknown. Both Female Only Male Only. Alone we fekty rare.

Standard Therapies Treatment The treatment of Felty syndrome is symptomatic and supportive.