Acute respiratory failure revealing adult-onset Still's disease. Diagnostic value of low glycosylated ferritin level

2005 ◽  
Vol 25 (5) ◽  
pp. 766-768 ◽  
Author(s):  
Charlotte Biron ◽  
Arnaud Chambellan ◽  
Christian Agard ◽  
Michele Denis ◽  
Patrick Germaud ◽  
...  
2020 ◽  
Vol 2020 ◽  
pp. 1-6
Author(s):  
G. D. E. Kodithuwakku ◽  
C. L. Fonseka ◽  
S. Nanayakkara ◽  
H. M. M. Herath

Background. Adult onset Still’s disease (AOSD) is a rare inflammatory disorder with a variety of clinical presentations. Even though pneumonitis and pleurisy are known to occur in AOSD, pulmonary onset presentations are exceedingly rare. Case Presentation. We present a 40-year-old male, presenting with fever and bilateral alveolar shadows with pleural effusions mimicking community-acquired severe pneumonia. He was initially treated as severe pneumonia with poor response to broad spectrum antibiotics. Subsequently, he was managed as AOSD-induced pneumonitis, as he fulfilled Yamaguchi criteria. Few weeks later, he developed macular rash and arthralgia with generalized lymphadenopathy with lymph node histology, showing Kikuchi lymphadenitis. He responded well to steroids and had a complete recovery. Conclusion. Non-infective causes of pneumonitis should be suspected in the setting of poorly resolving pneumonias, especially when microbiological and serological investigations does not support an infective etiology. Presence of systemic symptoms with arthralgia, rash, and disproportionately elevated ferritin level supports the diagnosis of AOSD. Kikuchi lymphadenitis is a reported association with AOSD, and there could be a causal link between the two disorders.


CHEST Journal ◽  
2021 ◽  
Vol 160 (4) ◽  
pp. A922-A923
Author(s):  
Ammar Ahmed ◽  
Corbin Edmondson ◽  
nitish singh nandu ◽  
Nehal Patel ◽  
Swetha Paduri ◽  
...  

2009 ◽  
Vol 36 (1) ◽  
pp. 156-162 ◽  
Author(s):  
SANG-WON LEE ◽  
YONG-BEOM PARK ◽  
JUNG-SOO SONG ◽  
SOO-KON LEE

Objective.To find a measure that can predict the disease course in patients with adult onset Still’s disease (AOSD).Methods.We retrospectively investigated the medical records of 71 hospitalized patients with AOSD. Patients were divided according to chronic and nonchronic disease course. The initial laboratory results were defined as those at the time of admission, the extremely deviated laboratory results as the highest or the lowest results, and the adjusted laboratory results as area under the curve divided by the days of hospitalization. All measures were compared and the odds ratio (OR) for the chronic disease pattern was assessed.Results.The mean age was 39.7 ± 13.5 years and women accounted for 63 of the total 71 (88.7%). Thirty patients (42.3%) had self-limited disease, 9 (12.7%) intermittent disease, and 23 (32.4%) the chronic disease pattern (32.4%). Nine patients (12.7%) died. The initial levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT) and ferritin, the highest levels of lactate dehydrogenase (LDH) and ferritin, and the adjusted level of ferritin in patients with chronic disease were significantly higher than those with nonchronic disease. Among them, only the middle range of the adjusted ferritin level (784.1~4120.0 ng/ml) was found to have a significant predictive value for the chronic disease pattern (OR 81.7, p = 0.007).Conclusion.A novel measure, the adjusted level of ferritin during the first hospitalization, might be useful to predict progression to chronic disease in patients with AOSD.


2014 ◽  
Vol 25 (2) ◽  
pp. 147-150
Author(s):  
Muhammet Emin Erdem ◽  
Seydahmet Akin ◽  
Asli Gocek Ozal ◽  
Adnan Helvaci ◽  
Selahattin Erturk ◽  
...  

2013 ◽  
Vol 4 (2) ◽  
pp. 52-54
Author(s):  
Mahmudur Rahman Siddiqui ◽  
Golam Kibria Khan ◽  
Md. Safiqul Islam ◽  
KM Ahasan Ahmed

Adult onset Still's disease (AOSD) is a chronic multi-system inflammatory disorder characterized by high spiking fever, polyarthralgia and skin rash. Lymphadenopathy is another prominent feature of adult onset Still's disease. We describe a 22 years old lady presented with fever, skin rashes and polyarthritis for 3 months. Examination revealed fever, typical skin rash, generalized lymphadenopathy and polyarthritis. On investigation there were neutrophilic leukocytosis, high ESR, high ferritin level, but RA test and ANA test were negative. All of her history, clinical examinations and laboratory findings fulfill the diagnostic Yamaguchi criteria for AOSD. With proper treatment, now she is completely symptoms free and leaving a healthy life. Anwer Khan Modern Medical College Journal Vol. 4, No. 2: July 2013, Pages 52-54 DOI: http://dx.doi.org/10.3329/akmmcj.v4i2.16944


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