Takayasu’s Arteritis

Authors

  • Sujeeb Rajbhandari Shahid Gangalal Nationl Heart Centre, Bansbari, Kathmandu, Nepal Tel: 00977-1-4371322, 00977-1-4371374. Fax 00977-1-4371123,

DOI:

https://doi.org/10.3126/njh.v6i1.18595

Keywords:

Takayasu’s Arteritis

Abstract

Takayasu’s arteritis is a disease of unknown etiology primarily affecting women aged less than 40 years. It is mainly seen in Asians and Africans. This condition is an aorto-arteritis and involves aorta and its major branches causing segmental narrowing or dilatation. Diminished or absent pulses and hypertension are common. Constitutional symptoms, including fever and weight loss, are often accompanied by elevation of acute phase markers. Diagnosis is made usually in quiescent or “cold phase” of the disease. Long-term complications are due mainly to arterial occlusion and related damage, including limb ischemia and renal failure.

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Published

2017-11-24

How to Cite

Rajbhandari, S. (2017). Takayasu’s Arteritis. Nepalese Heart Journal, 6(1), 48–52. https://doi.org/10.3126/njh.v6i1.18595

Issue

Section

Case Reports