🩺 TOACS FCPS Station · Hypertension & Blood Pressure Difference in Takayasu Arteritis

Nelson · 22nd Ed · Section 210.2 · “Takayasu arteritis – large vessel vasculitis; presents with hypertension, absent pulses, blood pressure asymmetry, bruits; diagnosis via MRA/CTA; treatment with glucocorticoids and biologics”
⏱️ 7 minutes · Examiner-led · Observed station
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📋 Takayasu Arteritis


🔍 Key clinical features to identify:

  • Hypertension – often severe, difficult to control
  • Blood pressure asymmetry – >10 mm Hg difference between arms
  • Absent or diminished pulses – 'pulseless disease'
  • Vascular bruits – over carotids, subclavians, abdomen
  • Constitutional symptoms – fever, weight loss, malaise

📋 Clinical scenario (examiner prompt)

A 12‑year‑old girl is brought to the clinic because of headaches and dizziness. On examination, her blood pressure in the right arm is 155/95 mm Hg, while in the left arm it is 130/80 mm Hg. The left radial pulse is weak and the right radial pulse is bounding. There is a bruit over the left carotid artery. The child has had fever, night sweats, and weight loss over the past 3 months. She is otherwise healthy with no history of cardiac disease.

Hypertension (155/95) BP difference 25 mm Hg Weak left radial pulse Carotid bruit

🧑‍⚕️ Examiner tasks · TOACS

1. Identify the diagnosis from the clinical context.

2. Describe the clinical features (hypertension, blood pressure asymmetry, absent pulses, bruits, constitutional symptoms).

3. Explain the underlying condition (Takayasu arteritis – large vessel vasculitis).

4. Discuss diagnosis and management (MRA/CTA, glucocorticoids, tocilizumab/TNF inhibitors).

⚠️ Key concept: Takayasu arteritis is a large vessel vasculitis involving the aorta and its major branches. Hypertension with blood pressure asymmetry (>10 mm Hg) and absent/diminished pulses are hallmark features. Constitutional symptoms (fever, weight loss) often precede vascular signs. Diagnosis is confirmed by MRA or CTA showing vessel wall thickening, stenosis, or aneurysm. Treatment is glucocorticoids plus tocilizumab or TNF inhibitors for refractory/steroid-dependent disease.

🎯 Expected answers (for examiners)

  • Diagnosis: Takayasu arteritis
  • Clinical features: Hypertension (often severe, renovascular), blood pressure asymmetry (>10 mm Hg between arms), absent/diminished pulses (pulseless disease), vascular bruits (carotid, subclavian, abdominal), claudication, constitutional symptoms (fever, malaise, weight loss)
  • Pathophysiology: Chronic granulomatous panarteritis of aorta and its major branches; leads to stenosis, occlusion, or aneurysm; female predominance (2-4:1)
  • Diagnostic workup: Four-limb blood pressure, MRA or CTA (vessel wall thickening, stenosis), PET-CT (inflammation), ESR/CRP (elevated), conventional angiography (luminal stenosis)
  • Treatment – First-line: Glucocorticoids (prednisone 1-2 mg/kg/day)
  • Treatment – Refractory/Steroid-dependent: Tocilizumab (IL-6 inhibitor) or TNF inhibitors (adalimumab, infliximab)
  • Hypertension management: ACE inhibitors (renovascular hypertension), calcium channel blockers, beta-blockers; control BP aggressively
📌 Takayasu arteritis – key points:
Vessels: Aorta and its major branches
Presenting: Hypertension, BP asymmetry, absent pulses, bruits
Diagnosis: MRA/CTA (vessel wall edema, stenosis)
Treatment: Glucocorticoids + tocilizumab/TNF inhibitor
Complications: Stroke, heart failure, renal failure, aneurysm

⚡ Quick FCPS‑style MCQ

A 12-year-old girl with hypertension, a 25 mm Hg blood pressure difference between arms, a weak left radial pulse, and a carotid bruit. The most likely diagnosis is:

A. Coarctation of aorta B. Takayasu arteritis C. Fibromuscular dysplasia D. Kawasaki disease

📌 Topic summary · Takayasu Arteritis (Hypertension & BP Asymmetry)

Definition
Large vessel vasculitis
Key feature
Hypertension + BP asymmetry
Imaging
MRA/CTA (stenosis, wall thickening)
Treatment
Glucocorticoids + biologics
Complications
Stroke, renal failure, aneurysm
Prognosis
80-90% 5-year survival
FeatureTakayasu Arteritis
DefinitionChronic granulomatous large vessel vasculitis involving aorta and its major branches
EpidemiologyFemale predominance (2-4:1), most common in Asian descent, onset 10-40 years
Presenting featuresHypertension (renal artery stenosis), blood pressure asymmetry (>10 mm Hg), absent/diminished pulses (pulseless disease), vascular bruits, claudication, constitutional symptoms (fever, weight loss)
DiagnosisEULAR/PRES criteria: angiographic abnormalities + ≥1 of: decreased pulses, BP difference >10 mm Hg, bruits, hypertension, elevated ESR/CRP
ImagingMRA with STIR (vessel wall edema), CTA, PET-CT (inflammation), conventional angiography (luminal stenosis)
First-line treatmentGlucocorticoids (prednisone 1-2 mg/kg/day)
Biologic therapyTocilizumab (IL-6 inhibitor) or TNF inhibitors (adalimumab, infliximab) for refractory/steroid-dependent disease
Hypertension managementACE inhibitors (first-line), calcium channel blockers, beta-blockers; aggressive BP control
Surgical interventionFor critical ischemia or refractory hypertension after inflammation controlled; avoid active inflammation
Prognosis5-year survival 80-90%; causes of death: stroke, heart failure, renal failure, aneurysm rupture
Source: Nelson Textbook of Pediatrics 22nd Ed · Section 210.2: Takayasu Arteritis · TOACS FCPS station.