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Journal of Dermatology and Clinical Research
Adult onset Still disease is a rare multisystemic autoinflammatory pathology of unknown etiology. Its clinical picture is very diverse, including fever, evanescent maculopapular rash and elevated inflammatory biomarker. It is associated with diseases such as arthritis, rheumatic fever, rheumatoid arthritis. We present the case of a woman with clinical
Suárez Efraín +10 more
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Adult onset Still disease is a rare multisystemic autoinflammatory pathology of unknown etiology. Its clinical picture is very diverse, including fever, evanescent maculopapular rash and elevated inflammatory biomarker. It is associated with diseases such as arthritis, rheumatic fever, rheumatoid arthritis. We present the case of a woman with clinical
Suárez Efraín +10 more
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JAMA, 1973
Two patients with adult-onset Still disease had a characteristic eruption most prominent during the febrile episodes, splenomegaly, and prolonged fever with temperature elevations to 40.6 C. Extensive investigation excluded other possible causes of fever. One patient partially responded to gold sodium thiomalate therapy.
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Two patients with adult-onset Still disease had a characteristic eruption most prominent during the febrile episodes, splenomegaly, and prolonged fever with temperature elevations to 40.6 C. Extensive investigation excluded other possible causes of fever. One patient partially responded to gold sodium thiomalate therapy.
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Nihon rinsho. Japanese journal of clinical medicine, 1999
Adult onset Still's disease was first reported by Bywaters in 1971. It is a systemic inflammatory disorder of unknown etiology, characterized by spiking fever, macular rash and polyarthritis. Although the prognosis is generally good, severe cases have been published. They include those with disseminated intravascular coagulation (DIC), hemophagocytosis,
H, Nara, A, Mimori
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Adult onset Still's disease was first reported by Bywaters in 1971. It is a systemic inflammatory disorder of unknown etiology, characterized by spiking fever, macular rash and polyarthritis. Although the prognosis is generally good, severe cases have been published. They include those with disseminated intravascular coagulation (DIC), hemophagocytosis,
H, Nara, A, Mimori
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2020
Still's disease is a systemic rheumatic disease of childhood which may persist into adulthood or may occur de novo in the adult population. It is classically distinguished by high fever, rash, arthritis, sore throat. Other clinical features may include lymphadenopathy, hepatosplenomegaly, pleuritis and pericarditis.
Ulusoy H., Bilgici A., Kuru Ö.
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Still's disease is a systemic rheumatic disease of childhood which may persist into adulthood or may occur de novo in the adult population. It is classically distinguished by high fever, rash, arthritis, sore throat. Other clinical features may include lymphadenopathy, hepatosplenomegaly, pleuritis and pericarditis.
Ulusoy H., Bilgici A., Kuru Ö.
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Revue medicale de Bruxelles, 1992
Retrospective case series for the last five years have focussed the attention of the authors on some clinical and biological patterns of adult onset Still's disease. Its diagnosis is made difficult because of the great diversity of clinical and biological signs. Organ failures complicate sometimes the disease, and may be fatal.
P, Nève, G, Decaux
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Retrospective case series for the last five years have focussed the attention of the authors on some clinical and biological patterns of adult onset Still's disease. Its diagnosis is made difficult because of the great diversity of clinical and biological signs. Organ failures complicate sometimes the disease, and may be fatal.
P, Nève, G, Decaux
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La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris, 1982
In 1971, less than one-hundred years after Still's publication (1897) concerning children, Bywaters described the adult-onset form of Still disease. Over one-hundred cases of this disorder have been recorded since. In adults, Still disease affects mainly women, and the average age at onset is twenty-seven.
C, Schwarzberg, P, Le Goff, G, Le Menn
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In 1971, less than one-hundred years after Still's publication (1897) concerning children, Bywaters described the adult-onset form of Still disease. Over one-hundred cases of this disorder have been recorded since. In adults, Still disease affects mainly women, and the average age at onset is twenty-seven.
C, Schwarzberg, P, Le Goff, G, Le Menn
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