Takayasu's arteritis

Authors

  • Viviana Hernández de Mezerville Servicio de Medicina, Hospital Dr. Rafael A. Calderón Guardia, Caja Costarricense de Seguro Social
  • Carlos Bravo Rojas Servicio de Medicina, Hospital Dr. Rafael A. Calderón Guardia, Caja Costarricense de Seguro Social
  • Eduardo Fiedler Velásquez Servicio de Medicina, Hospital Dr. Rafael A. Calderón Guardia, Caja Costarricense de Seguro Social
  • Charles Gourzong Taylor Servicio de Medicina, Hospital Dr. Rafael A. Calderón Guardia, Caja Costarricense de Seguro Social

DOI:

https://doi.org/10.51481/amc.v49i3.324

Keywords:

Takayasu, aortoarteritis, vasculitis

Abstract

We report a case of woman with Tayakasu`s Arteritis (AT) who had decreased arterial pulses in the right arm along with arterial hypertension. AT is a chronic vasculitis of unknown etiology involving mainly the aorta and its branches. It is most prevalent in women of reproductive age but it can occur at any age. The clinical presentation is variable and the symptoms are ischemic secondary to stenotic lesions or thrombus formation in the arterial tree. These lesions can lead to secondary hypertension, retinopathy, cerebrovascular disease, cardiopathy and premature death. The diagnosis of AT should be suspected in young women with diminished or absent peripheral pulses, discrepancies in blood pressure, and arterial bruits. It is confirmed with by angiogram. Therapeutic options include glucocorticoids, inmunosupprant agents and treatment of its complications.

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References

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Published

2007-07-01

How to Cite

Takayasu’s arteritis. (2007). Acta Médica Costarricense , 49(3), 167-169. https://doi.org/10.51481/amc.v49i3.324