No abstract available.
Adult ; Humans ; Still's Disease, Adult-Onset

No abstract available.
Adult* ; Humans ; Still's Disease, Adult-Onset*

No abstract available.
Fever ; Humans ; Still's Disease, Adult-Onset* ; Urticaria*

No abstract available.
Blood Platelets* ; Still's Disease, Adult-Onset*

No abstract available.
Adult ; Bone Marrow ; Humans ; Still's Disease, Adult-Onset

Adult onset Still's disease is a rare inflammatory disease characterized by spiking fevers, arthritis/ arthralgias, typical salmon-colored bumpy rash, pharyngalgia, myalgia and possible involvement of visceral organs. The diagnosis is exclusively based on clinical symptoms, according to the criteria, after the exclusion of well-known infectious, neoplastic, or other autoimmune/autoinflammatory disorders. This report includes one case of adult onset Still's disease with the initial symptom of pharyngalgia.
Adult ; Humans ; Pharyngitis ; Rare Diseases ; Still's Disease, Adult-Onset ; diagnosis

Up to date, symptomatic neonate who needed treatments due to mother's AOSD has not been reported. We experienced a neonate born of mother diagnosed with AOSD a week before delivery. Despite treatment, the mother's symptoms had not been improved until delivery. Our patient was affected by her mother's condition, and exhibited several symptoms (fever over one week, poor activity, poor feeding) since 5 days of age, with thrombocytopenia, negative results on viral and bacterial studies, and elevation of CRP, OT/PT and ferritin. Treatment with steroid, NSAID and IV immunoglobulin was started on 14 days of age under the impression of possible maternal effects from uncontrolled AOSD of mother. The symptoms were gradually improved. Ferritin level was decreased, others were normal on 29 days of age. We present this case for the first time as effects of maternal AOSD on newborn, with review of literature.
Adult* ; Ferritins ; Humans ; Immunoglobulins ; Infant, Newborn* ; Mothers* ; Pregnancy ; Still's Disease, Adult-Onset* ; Thrombocytopenia

No abstract available.
Adult* ; Disseminated Intravascular Coagulation* ; Humans ; Multiple Organ Failure* ; Still's Disease, Adult-Onset*

OBJECTIVE: Adult onset Still s disease is an acute systemic inflammatory disorder. There are no pathognomonic symptoms or specific laboratory abnormalities. In recent reports, serum ferritin concentration is increased in active disease phase and decreased after defervescence. Our purpose was to determine the clinical significance of serum ferritin as an indicator for disease activity. METHODS: Seven patients who were diagnosed as adult onset Still s disease at Samsung Medical Center between October 1994 and March 1997, were reviewed. In these patients we checked leukocyte count, ESR, CRP and serum ferritin concentrations at the time of diagnosis and during follow-up periods and recorded febrile events during follow-up periods. RESULTS: At the time of diagnosis and during febrile periods, the concentrations of ferritin were extremely high(927ng/ml to 96,650ng/ml normal 10-290.8 ng/ml). The values were unrelated to other manifestations of the disease or laboratory findings. The ferritin concentrations decreased rapidly after adequate treatment. Eleven febrile reattacks happened in 7 patients. Serum ferritin concentrations were increased in 8 febrile attacks, while leukocyte count, ESR, and CRP were increased in 5, 5, 6 febrile attacks respectively, There were 10 events of increased serum ferritin concentrations in 7 patients during follow-up periods and 8 events were related with fever. The increases of other laboratory tests were similar. CONCLUSIONS: In all patients, serum ferritin concentrations were increased at the time of diagnosis and closely related to fever. During follow-up periods, serum ferritin concentrations are helpful in monitoring disease activity and guiding decisions about treatment.
Adult* ; Diagnosis ; Ferritins* ; Fever ; Follow-Up Studies ; Humans ; Leukocyte Count ; Still's Disease, Adult-Onset*

Adult-onset of Still's disease is a rare systemic rheumatic disorder. It involves various organs including the lungs and pleura. We report here the CT findings of a patient with the thoracic manifestations of Still's disease, including axillary and mediastinal lymphadenopathies, pleural and pericardial effusions and infiltrations in both lung bases.
Arthritis, Rheumatoid ; Humans ; Lung ; Pericardial Effusion ; Pleura ; Still's Disease, Adult-Onset*