scholarly journals Recurrent Pneumonia in Kartagener'S Syndrome with Rheumatoid Arthritis

Author(s):  
P. Kirkpatrick ◽  
E. Quarshie ◽  
P. Jamindar ◽  
V.S. Taskar
2016 ◽  
Vol 2016 ◽  
pp. 1-5 ◽  
Author(s):  
Hussein Halabi ◽  
Israa Mulla

We report a case of an 18-year-old girl who presented to our hospital with history of recurrent respiratory infections, amenorrhea, and symmetric polyarthritis. She was diagnosed with rheumatoid arthritis (RA), Kartagener’s syndrome (KS), and hyperprolactinemia. There have been very few case reports in the literature of RA occurring in the setting of KS, theoretically proposed to be due to chronic stimulation of the immune system by recurrent infections. Furthermore, hyperprolactinemia has been hypothesized to mirror RA disease activity and case reports of treatment with dopamine agonists have led to the speculation of whether or not they represent a new line of experimental treatment in the future. Our patient was found to have both KS and hyperprolactinemia together in the setting of RA, and based on our literature search, this is the first reported case of such a combination. This strikes a very intriguing question: are these three conditions interlinked by a yet to be defined association? And treatment of which condition leads to the resolution of the other?


2000 ◽  
Vol 42 (3) ◽  
pp. 316-318 ◽  
Author(s):  
Yukihiko Kawasaki ◽  
Junzo Suzuki ◽  
Tatsuhiko Sike ◽  
Masato Isome ◽  
Ruriko Nozawa ◽  
...  

2014 ◽  
Vol 53 (3) ◽  
pp. 269-274 ◽  
Author(s):  
Satoshi Takasaki ◽  
Shu Yamakage ◽  
Sachiko Fukase ◽  
Toshiyuki Takahashi

2001 ◽  
Vol 20 (4) ◽  
pp. 282-284 ◽  
Author(s):  
L. Riente ◽  
P. Fadda ◽  
M. Mazzantini ◽  
S. Frigelli ◽  
B. Fattori ◽  
...  

Author(s):  
George Price ◽  
Lizardo Cerezo

Ultrastructural defects of ciliary structure have been known to cause recurrent sino-respiratory infection concurrent with Kartagener's syndrome. (1,2,3) These defects are also known to cause infertility in both males and females. (4) Overall, the defects are defined as the Immotile, or Dyskinetic Cilia Syndrome (DCS). Several ultrastructural findings have been described, including decreased number of cilia, multidirection orientation, fused and compound cilia, membrane blebs, excess matrix in the axoneme, missing outer tubular doublets, translocated doublets, defective radial spokes and dynein arms. A rare but noteworthy ultrastructural finding in DCS is the predominance of microvilli-like structures on the luminal surface of the respiratory epithelium. (5,6) These permanent surface modifications of the apical respiratory epithelium no longer resemble cilia but reflect the ultrastructure of stereocilia, similar to that found in the epidydimal epithelium. Like microvilli, stereocilia are devoid of microtubular ultrastructure in comparison with true cilia.


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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