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Combination of Methotrexate and Leflunomide for Adult-onset Still's Disease: A Case Report and Literature Review

Lee EE, Kim MJ, Song YW, Park JK

The treatment of adult-onset Still's disease (AOSD) aims to control systemic inflammation and prevent organ damage. Systemic inflammation can be controlled with corticosteroid (CS) monotherapy in most cases. However, symptoms...
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Red blood cell distribution width is useful in discriminating adult onset Still's disease and sepsis within 24 hours after hospitalization

Park HJ, Song J, Park YB, Lee SK, Lee SW

BACKGROUND/AIMS: Red blood cell distribution width (RDW) is a value representing the heterogeneity in the size of red blood cell, and it is usually used in distinguishing types of anaemia....
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Adult-onset Still's Disease as the First Manifestation of Cerebral Infarction: a Case Report

Choi JK, Seo YJ, Kim DY

Adult-onset Still's disease (AOSD) is a rare systemic febrile disorder of unknown etiology. AOSD is characterized by spiking fever, arthralgia, sore throat, skin rash, and multi-organ involvement but is difficult...
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A case of adult-onset Still's disease accompanied by pseudo-gray platelet syndrome

Miyakawa S, Ohe M, Shida H, Horita T, Furuya K, Hashino S

No abstract available.
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A Case of Atypical Adult-onset Still's Disease That Presented with Unique Histopathologic Findings

Kim DJ, Lee DY, Lee SK, Kim MS, Lee UH, Hahm JH

  • KMID: 2251149
  • Korean J Dermatol.
  • 2016 May;54(4):288-292.
Adult-onset Still's disease (AOSD) is an uncommon disorder characterized by fever, polyarthralgia, elevated white blood cell count, and maculopapular rash, the histologic features of which have not been well known....
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Adult-Onset Still's Disease with Thrombotic Thrombocytopenic Purpura

Lee TH, Lee JM, Lee SY, Cho NH, Son CN, Kim JM, Kim SH

Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disorder that affects multiple organs and is fatal in some cases. Thrombotic thrombocytopenic purpura (TTP), another rare disease, is characterized by...
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Endomyocardial Biopsy and Magnetic Resonance Imaging of Acute Myocarditis with Adult-Onset Still's Disease

Yamazoe M, Mizuno A, Suyama Y, Nishi Y, Suzuki K, Niwa K, Okada M

A 36-year-old female with a high-grade fever and epigastric abdominal pain was prescribed antibiotics, but developed hypoxia and dyspnea. An echocardiography revealed diffuse hypokinesis and massive pericardial effusion, after which...
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Adult Onset Still's Disease Developed in Chronic Urticaria Patient

Chun SW, Lee SY, Son HO, Ro BI, Cho HK

  • KMID: 2089044
  • Korean J Dermatol.
  • 2014 Sep;52(9):665-666.
No abstract available.
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A Case of Adult Onset Still's Disease with Severe Pneumonitis Treated with Anakinra

Cho SH, Kim OZ, Cho SW, Lim DM, An SK, Kim CK

Adult onset Still's disease (AOSD) is a systemic autoinflammatory disorder that presents with recurrent fever, extreme fatigue, and joint pain. Pulmonary involvement is not uncommon and, although rare, severe pneumonitis...
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A Case of Musculoskeletal Tuberculosis Mimicking Adult-Onset Still's Disease

Cho JK, Kim MS, Shin JH, Jeong YS, Kim JW, Choi JP, Choi BY

  • KMID: 2269348
  • Korean J Med.
  • 2014 Jun;86(6):785-790.
A 46-year-old man was admitted to our hospital because of a fever of unknown origin. The patient had a skin rash, arthralgia, and hepatosplenomegaly. Laboratory tests showed leukemoid leukocytosis, a...
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A Case Report of Renal Involvement in Adult-Onset Still's Disease over Age 70

Yoon GS, Park W, Baek JH, Han JY, Jung KH, Lim MJ, Joo K, Kwon SR

Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disease characterized by spiking fever, arthralgia, salmon pink rash, neutrophilic leukocytosis, and multi-organ involvement. Although renal involvement may appear in some...
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Adult Onset Still's Disease Misunderstood as Sepsis with Bile Peritonitis

Han SM, Kim WW, Chung CW, Lee KP, Lee KS

  • KMID: 2040622
  • J Korean Surg Soc.
  • 2007 Jun;72(6):505-508.
Adult onset Still's disease (AOSD) is a rare systemic inflammatory disorder of an unknown etiology, and its major clinical manifestations include high spiking fever, polyarthralgia, salmon-colored evanescent rash and neutrophilic...
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Adult-onset Still's Disease with Dysphagia: Case report

Cho YM, Choi IS, Jung SH, Kim JH, Lee SG

  • KMID: 1851588
  • J Korean Acad Rehabil Med.
  • 2007 Jun;31(3):361-365.
We experienced a case of adult-onset Still's disease with dysphagia of soft tissue origin. A 38-year-old woman was admitted for intermittent high spiking fever, diffuse pain and swelling on anterior...
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A Case of Pulmonary Hypertension in a Patient with Adult-onset Still's Disease

Woo JH, Chang SJ, Yoo DH

Pulmonary hypertension is one of the serious complications of autoimmune rheumatic disease, and it is becoming an important cause of morbidity and premature death. Pulmonary involvement occurs occasionally in...
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Two Cases of Adult Onset Still's Disease with Concomitant Hemophagocytic Syndrome

Kim HS, Park KW, Kim SK, Kim JY, Park SH, Shin JH, Kim SG, Choe JY

Adult onset Still's disease is an rare inflammatory disease with the characteristic of fever, skin rash, arthralgia or arthritis, lymphadenopathy, leukocytosis and multiple systemic organ involvement. Its accurate pathogenesis has...
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Two Cases of Adult Onset Still's Disease with Disseminated Intravascular Coagulation and Multiple Organ Involvement Treated with Cyclosporine

Shim EJ, Lee YH, Lee J

Adult onset Still's disease (AOSD) is a systemic inflammatory disorder of unknown etiology and pathogenesis. It is characterized by spiking fever, evanescent skin rash, arthralgia or arthritis, hepatosplenomegaly and laboratory...
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Adult Onset Still's Disease

Lee DH, Park JW, Hyun JW, Kim DH, Suh YS

  • KMID: 2294530
  • J Korean Acad Fam Med.
  • 2007 Mar;28(3):210-213.
Adult onset Still's disease (AOSD) is an uncommon acute systemic inflammatory disease of unknown origin. The clinical features include high spiking fever, arthralgia or arthritis, transient maculopapular rash, lymphadenopathy, hepatosplenomegaly,...
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Successful Treatment with Etanercept in a Patient with Adult-onset Still's Disease

Woo H, Kim OK, Lee GH, Park JJ, Lee SS, Park YW

  • KMID: 2202205
  • J Korean Rheum Assoc.
  • 2006 Dec;13(4):306-310.
Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disorder of unknown etiology. Non-steroidal anti-inflammatory drugs (NSAIDs), steroids, disease modifying anti-rheumatic drugs (DMARDs), immunosuppressives and intravenous immunoglobulin (IVIG) have been...
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Association of Interleukin-18 Polymorphisms with Adult Onset Still's Disease in Korea

Her MY, Kim SK, Sung YK, Lee HS, Uhm WS, Kim TH, Jun JB, Chung WT, Choe JY, Chang HK, Bae SC, Yoo DH

  • KMID: 1581080
  • J Korean Rheum Assoc.
  • 2006 Jun;13(2):116-122.
OBJECTIVE: It has been suggested that overproduction of interleukin -18 (IL-18) may contribute to the pathogenesis of adult onset Still's disease (AOSD). Recently, positive association between a polymorphism in the...
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Thoracic CT Findings of Adult-Onset Still's Disease: A Case Report

Choi SY, Kim K, Lee JW, Lee SY, Hong YS

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...
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