Takayasu arteritis presenting with malignant hypertension; a rare manifestation of a rare disease: a case report and review of the literature

Trop Doct. 2017 Jan;47(1):60-63. doi: 10.1177/0049475516648062. Epub 2016 May 22.

Abstract

Takayasu arteritis (TA) is a chronic inflammatory and obliterative disease of large vessels, which mainly affects the aorta and its major branches. TA can lead to renal failure and renovascular hypertension in 60% of patients; it is rare in children aged <10 years and, more rarely, it presents with malignant hypertension in the paediatric age group. Here we present a case of 9-year-old boy with TA who presented with malignant hypertension and required surgical intervention to control the blood pressure. Subsequently, his medications were titrated using 24 h ambulatory blood pressure monitoring (ABPM) and is doing well on follow-up.

Keywords: Takayasu arteritis (TA); malignant hypertension; nephrectomy.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Antihypertensive Agents / therapeutic use
  • Child
  • Humans
  • Hypertension, Malignant / diagnostic imaging
  • Hypertension, Malignant / drug therapy
  • Hypertension, Malignant / etiology*
  • Hypertension, Malignant / surgery
  • Male
  • Nephrectomy
  • Rare Diseases
  • Takayasu Arteritis / complications*
  • Takayasu Arteritis / diagnosis

Substances

  • Antihypertensive Agents