scholarly journals Elevated autoantibody content in rheumatoid arthritis synovia with lymphoid aggregates and the effect of rituximab

2008 ◽  
Vol 10 (5) ◽  
pp. R105 ◽  
Author(s):  
Sanna Rosengren ◽  
Nathan Wei ◽  
Kenneth C Kalunian ◽  
Nathan J Zvaifler ◽  
Arthur Kavanaugh ◽  
...  
2007 ◽  
Vol 123 ◽  
pp. S93
Author(s):  
Tineke Cantaert ◽  
Trieneke Timmer ◽  
Bernard Vandooren ◽  
Carla Wijbrandts ◽  
Rogier Thurlings ◽  
...  

2012 ◽  
Vol 136 (10) ◽  
pp. 1253-1258 ◽  
Author(s):  
Nicole A. Cipriani ◽  
Mary Strek ◽  
Imre Noth ◽  
Ilyssa O. Gordon ◽  
Jeff Charbeneau ◽  
...  

Context.—Usual interstitial pneumonia (UIP) is a common chronic interstitial pneumonitis. It can occur idiopathically (I-UIP) or in the setting of systemic connective tissue disease (CTD-UIP). Some studies suggest that CTD-UIP has a better prognosis than I-UIP. The histologic differences between CTD-UIP and I-UIP are not clearly defined. Objective.—The purpose of this study was to evaluate histologic criteria that may differentiate CTD-UIP from I-UIP, including fibroblastic foci (FFs), lymphoid aggregates (LAs), and the presence of nonspecific interstitial pneumonia pattern. Design.—Thirty-five patients with histologic diagnoses of UIP were identified (27 biopsies [77%]; 8 explants [23%]). Biopsy slides were scanned and analyzed quantitatively for FF size, FF area, LA size, and LA area. Biopsy and explant slides were examined qualitatively for the presence of a nonspecific interstitial pneumonia pattern in areas away from UIP fibrosis. Results.—Of 27 biopsies, the number and size of FFs in CTD-UIP were smaller than they were in I-UIP. The number and size of LAs were larger in patients with rheumatoid arthritis than they were in patients with I-UIP. There was no interobserver variability among 3 pathologists using this quantitative system. Of 35 biopsies and explants, there was a higher prevalence of the nonspecific interstitial pneumonia pattern among patients with CTD-UIP than there was among patients with I-UIP (P = .005). Conclusions.—Patients with CTD-UIP had fewer, smaller FFs than did patients with I-UIP, and patients with rheumatoid arthritis-UIP had more, larger LAs than did patients with I-UIP. Of importance, the coexistence of UIP and the nonspecific interstitial pneumonia patterns was one of the most salient features in distinguishing CTD-UIP from I-UIP because CTD-UIP demonstrated an increased prevalence of multilobar, cellular, nonspecific interstitial pneumonia patterns in areas away from the UIP fibrosis.


PLoS ONE ◽  
2017 ◽  
Vol 12 (8) ◽  
pp. e0182904 ◽  
Author(s):  
Jani Luukkonen ◽  
Laia Mira Pascual ◽  
Christina Patlaka ◽  
Pernilla Lång ◽  
Sanna Turunen ◽  
...  

2001 ◽  
Vol 28 (1) ◽  
pp. 89-93 ◽  
Author(s):  
J. R. Garcia-Lozano ◽  
M. F. Gonzalez-Escribano ◽  
A. Valenzuela ◽  
A. Garcia ◽  
A. Nunez-Roldan

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