Takayasu's Arteritis and Rheumatoid Arthritis
- 1 November 1964
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of internal medicine (1960)
- Vol. 114 (5) , 594-600
- https://doi.org/10.1001/archinte.1964.03860110064003
Abstract
Takayasu's arteritis could be briefly defined as an inflammatory process occurring almost exclusively in females in the reproductive age and most commonly involving the great vessels arising from the aortic arch resulting in stenosis and eventually in obliteration or thrombosis. It has been given various names, such as pulseless disease, aortic arch syndrome, branchial arteritis, chronic subclaviocarotid syndrome, syndrome of obliteration of the supra-aortic branches, brachiocephalic arteritis, young female arteritis, and reversed coarctation. Judge et al1 have discussed the different nomenclatures and preferred the term "Takayasu's arteritis," which we will follow in the present report. It has been said recently1 that the etiology of this disorder remains as obscure today as when Savory first described it in 1856.2 In a few early cases from Japan, tuberculous infection was incriminated, because a positive tuberculin test was present in all of the cases.3 Harbitz4 suspected a streptococcalThis publication has 3 references indexed in Scilit:
- NATURAL HISTORY OF TAKAYASUS ARTERIOPATHY1964
- Aortic Arch Syndrome with Special Reference to Rheumatoid ArteritisActa Medica Scandinavica, 1961
- ON THE PULSELESS DISEASE OUTSIDE OF JAPAN1954