Published online Oct 16, 2021. doi: 10.12998/wjcc.v9.i29.8831
Peer-review started: June 8, 2021
First decision: June 25, 2021
Revised: June 28, 2021
Accepted: August 17, 2021
Article in press: August 17, 2021
Published online: October 16, 2021
Processing time: 129 Days and 2.6 Hours
Eosinophilic fasciitis (EF) is a rare disease characterized by inflammation of the fascia with immune system involvement. Failure to promptly diagnose and treat this disease can seriously affect the quality of life of patients. However, no clear and uniform criteria for diagnosis and treatment exist.
In this paper, we report two cases of EF, both of which showed symmetrical limb swelling and rigidity, increased eosinophils in the peripheral blood and bone marrow, increased red blood cell sedimentation rate, increased antinuclear antibody titer, and pathological changes in the tissues such as eosinophil and lymphocyte infiltration. Both patients were treated with hormones and cyclosporine, and showed significant improvements in their conditions.
EF is an autoimmune disease causing swelling and sclerosis of the fascia and eosinophilia. It is diagnosable by magnetic resonance imaging, positron emission tomography-computed tomography, blood routine tests, and bone marrow puncture. Glucocorticoids and immunosuppressants are effective treatments.
Core Tip: Eosinophilic fasciitis is a rare disease that can affect the immune system. Currently, there are no clear diagnostic criteria for this entity. Because of the rarity of eosinophilic fasciitis, patients may go to orthopedics department, dermatology department, etc., for dyskinesias, skin lesions, etc., so the disease is diagnosis and treatment will be restricted in many ways. This article records two eosinophilic fasciitis patients, in order to provide more detailed and comprehensive information for the clinical diagnosis and treatment of this rare disease.