scholarly journals Fever as the Sole Presentation of Giant Cell Arteritis: A Near Miss

2019 ◽  
Vol 7 ◽  
pp. 232470961985022 ◽  
Author(s):  
Pooja Poudel ◽  
Thein Swe ◽  
Michael Wiilliams ◽  
Eduardo Bonilla

Giant cell arteritis (GCA) presenting solely as fever is very rare. Usually, it manifests with typical features such as visual problems, headache, jaw claudication, or it can be associated with polymyalgia rheumatica. We present a case of a patient with GCA who presented only with prolonged fever. The cause of fever could not be initially identified in spite of a comprehensive workup. The patient was started on steroids for presumed GCA resulting in the resolution of fever. It is of paramount importance to consider GCA in the differential diagnosis of fever of unknown origin. Early diagnosis with effective treatment is crucial since the mortality rate remains high for untreated cases.

Author(s):  
Lorenzo Grazioli Gauthier ◽  
Natalie Marcoli ◽  
Gianluca Vanini ◽  
Enos Bernasconi ◽  
Dea Degabriel

Giant cell arteritis (GCA), or Horton’s arteritis, presenting solely as fever is very rare. Usually, it manifests with typical features such as visual problems, headache and jaw claudication, or it can be associated with polymyalgia rheumatica. We describe the case of a patient with GCA who presented only with prolonged fever, the cause of which was not determined by diagnostic tests.


2012 ◽  
Vol 19 (5) ◽  
pp. 299 ◽  
Author(s):  
Mi Il Kang ◽  
Hee Jin Park ◽  
Hyae Min Jeon ◽  
Yoon Kang ◽  
Sang Won Lee ◽  
...  

2006 ◽  
Vol 95 (02) ◽  
pp. 390-392 ◽  
Author(s):  
Olivier Chavaillaz ◽  
Salah Gueddi ◽  
Sophia Taylor ◽  
Hans Stalder ◽  
Marc Righini

2009 ◽  
Vol 24 (4) ◽  
pp. 532-536 ◽  
Author(s):  
Valentin S. Schäfer ◽  
Kenneth J. Warrington ◽  
Eric E. Williamson ◽  
Tanaz A. Kermani

2013 ◽  
Vol 71 (Suppl 3) ◽  
pp. 682.14-682
Author(s):  
R. Talarico ◽  
A. d’Ascanio ◽  
C. Stagnaro ◽  
C. Ferrari ◽  
S. Bombardieri

Reumatismo ◽  
2016 ◽  
Vol 67 (4) ◽  
pp. 165 ◽  
Author(s):  
T. Aguiar ◽  
M. B. Vincent

Giant cell arteritis (GCA), a systemic vasculitis of unknown origin, may appear rarely as a paraneoplastic syndrome. Cases secondary to pulmonary neuroendocrine tumors have not been reported. A 75-year-old female developed prednisone-responsive GCA/polymyalgia rheumatica (PMR) shortly followed by syndrome of inappropriate antidiuretic hormone secretion. An 8 mm carcinoid lung tumor with positron emission tomography normal uptake was found. After a thoracoscopic tumor resection the patient experienced complete clinical and laboratory remission. This is the first report of GCA with PMR in the context of carcinoid lung tumor. It emphasizes the role of paraneoplastic vasculitis as a possible cause of GCA.


2017 ◽  
Vol 76 (1) ◽  
pp. 83-86 ◽  
Author(s):  
K. Hofheinz ◽  
S. Bertz ◽  
J. Wacker ◽  
G. Schett ◽  
B. Manger

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