Is there a cure for Felty syndrome?
There is no definitive treatment for Felty syndrome. The management for FS is supportive and directed towards controlling the underlying RA while also improving the neutropenia to prevent life-threatening infections.
Is Felty syndrome genetic?
The cause of Felty’s syndrome is unknown, but doctors believe it’s a genetic condition. It’s possible that the affected individuals need only one abnormal gene to develop the disease.
Who is Felty?
Felty’s syndrome is a rare, potentially serious disorder that is defined by the presence of three conditions: rheumatoid arthritis (RA), an enlarged spleen (splenomegaly) and a decreased white blood cell count (neutropenia), which causes repeated infections.
How is Felty syndrome diagnosed?
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.e. the presence of rheumatoid arthritis, low white blood count, and splenomegaly).
How is Felty’s syndrome diagnosed?
What are the best treatments for Felty syndrome?
Approach Considerations. The best way of treating Felty syndrome (FS) is to control the underlying rheumatoid arthritis (RA).
What are the typical symptoms of Felty’s syndrome?
Fatigue
Are there typical signs of Felty’s syndrome?
The signs and symptoms of Felty’s Syndrome are consistent with those of RA, such as pain or stiffness in multiple joints, warmth or redness over joints and lumpy growths around some joints, such as elbows, hands or feet. Additionally, people with FS may have symptoms such as fatigue, fever, weight loss, skin discolouration and/or ulceration.
Are blood tests used to diagnose Felty’s syndrome?
Blood work for Felty syndrome will include a complete blood cell count. Your doctor may also request a blood lab test to check for neutropenia, or exceptionally low neutrophils white blood cells. These blood cells help you to fight off bacterial infections .