Cardiovascular

Takayasu Arteritis in a 15-Year-Old Male Presenting with Constitutional Symptoms and Upper Limb Pulse Deficit: A Case Report a Resource-Limited Settings.

TL;DR

A 15-year-old male in Somaliland was diagnosed with Takayasu arteritis through clinical suspicion and bilateral pulse palpation without advanced imaging, demonstrating that 'timely diagnosis and intervention are possible in developing healthcare systems.'

Key Findings

A 15-year-old male presented with several months of constitutional symptoms before developing more acute findings that led to diagnosis of Takayasu arteritis.

  • Constitutional symptoms included low-grade fever, easy fatigability, and progressive bilateral multiple joint pain lasting several months
  • Three weeks prior to diagnosis, he developed chest pain, vomiting, and significant weight loss
  • The patient had a history of BCG vaccination and no known tuberculosis exposure
  • The patient was male and located in Somaliland (East Africa), which represents a less common demographic for Takayasu arteritis

Physical examination revealed absence of left radial and brachial pulses with asymmetric blood pressure as a key diagnostic finding.

  • Left radial and brachial pulses were absent on examination
  • Right arm blood pressure was 130/87 mmHg; blood pressure could not be measured in the left arm due to blocked blood flow
  • Cardiac auscultation was unremarkable
  • Vital signs were otherwise stable
  • Bilateral pulse palpation was identified as the critical clinical maneuver that bridged the diagnostic gap

Laboratory findings showed normocytic anemia and elevated inflammatory markers consistent with active vasculitis.

  • Hemoglobin was 12 g/dL, indicating normocytic anemia
  • Erythrocyte sedimentation rate (ESR) was elevated at 70 mm/hr
  • Rheumatoid factor was negative
  • Renal function was normal
  • Echocardiography was normal

CT angiography demonstrated extensive large-vessel involvement affecting multiple arterial territories.

  • CTA of the abdominal aorta showed concentric arterial wall thickening of the superior mesenteric artery (SMA) with severe stenosis and collateral formation
  • CTA of the left upper limb revealed long-segment concentric thickening involving the left common carotid, subclavian, axillary, and proximal brachial arteries
  • Focal occlusion of the brachial artery with distal collaterals was identified
  • Renal arteries were spared
  • Diagnosis was made without advanced imaging modalities such as PET or MRA

The patient was initiated on prednisolone 60 mg daily and methotrexate with one-month follow-up arranged.

  • Prednisolone was prescribed at 60 mg daily, described as the 'maximum dose'
  • Methotrexate was added as a steroid-sparing immunosuppressive agent
  • Follow-up was arranged for one month
  • Treatment was initiated in a resource-limited setting without specialized rheumatology services

This case highlights that Takayasu arteritis can be diagnosed in resource-limited settings through clinical suspicion and physical examination without advanced imaging.

  • The case represents a 'novel diagnostic pathway in a resource-limited setting' per the authors
  • High index of clinical suspicion and meticulous physical examination—specifically bilateral pulse palpation—were identified as sufficient to bridge the gap left by lack of specialized rheumatology services
  • The case demonstrates that TA can occur in a teenage male in East Africa, expanding the recognized demographic beyond young women from Asia or South America
  • Authors note that the case shows 'even without advanced imaging like PET or MRA, timely diagnosis and intervention are possible in developing healthcare systems'

What This Means

This research describes a single case of a 15-year-old boy in Somaliland (East Africa) who was diagnosed with Takayasu arteritis, a rare autoimmune disease where the immune system attacks the body's large blood vessels, causing them to thicken and narrow. The boy had been experiencing vague symptoms—low-grade fever, fatigue, joint pain, and weight loss—for several months before doctors discovered a crucial clue during physical examination: there was no detectable pulse in his left wrist or arm, and blood pressure could not even be measured in his left arm. A CT scan confirmed that several major arteries, including those supplying his left arm, part of his brain, and his intestines, were severely narrowed or blocked. He was treated with high-dose steroids and methotrexate, a medication that suppresses immune system overactivity. This research suggests that Takayasu arteritis, though most commonly reported in young women from Asia and South America, can also occur in young males in East Africa, meaning clinicians worldwide should remain alert to this diagnosis. The case emphasizes that a simple, low-cost physical examination step—checking and comparing pulses in both arms—can detect a serious vascular disease even when expensive or specialized equipment is unavailable. The authors argue that even in healthcare settings with limited resources, early diagnosis of this condition is achievable through careful clinical assessment combined with widely available CT imaging. The practical implication highlighted by this case is that young people presenting with prolonged fever, unexplained weight loss, and joint pain should have their pulses checked in both arms as part of routine examination. Early detection of Takayasu arteritis matters because the disease can lead to stroke, organ damage, and other life-threatening complications if left untreated. The case underscores the continuing importance of thorough physical examination skills in settings where advanced diagnostic tools may not be readily available.

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Citation

Mohamed H, Botan N, Ahmed S, Qawdhan M. (2026). Takayasu Arteritis in a 15-Year-Old Male Presenting with Constitutional Symptoms and Upper Limb Pulse Deficit: A Case Report a Resource-Limited Settings.. International medical case reports journal. https://doi.org/10.2147/IMCRJ.S583050