Systemic manifestations of Takayasu arteritis: The expanding spectrum
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Takayasu's arteritis: Review of epidemiology and etiopathogenesis
2015, Indian Journal of RheumatologyCitation Excerpt :In vitro lupus erythematosus cells have been described in a few cases of TA alongside the clinical manifestations. Sharma et al. reported TA in association with nephritic syndrome/amyloidosis, glomerulo-nephritis, and interstitial lung disease.99 Subsequently, serum complements, antineutrophil cytoplasmic antibody (ANCA), antinuclear antibodies (ANA), and antiphospholipid antibodies have been evaluated in different studies but the results are inconsistent.42,100,101
Pericardial effusion as primary manifestation of Takayasu arteritis
2010, International Journal of CardiologyCitation Excerpt :TA is a chronic primary vasculitis of unknown etiology [1], affecting young women in 80–90% of cases with greatest prevalence in Asians. Early diagnosis of TA is extremely difficult, because all symptoms in the early phase such as fatigue, low-grade fever, malaise, arthralgia and a loss of body weight are all non-specific [2]. At this early phase, vascular changes may not be sufficiently advanced, hence the specific symptoms like cold extremities, claudication or blood pressure differences may be absent.
Glomerular disease associated with Takayasu arteritis: 6 Cases analysis and review of the literature
2009, Chinese Medical Sciences JournalTakayasu's arteritis
2003, Anales de Pediatria