Carotid Tumours

Carotid tumours are rare growths that develop in or around the carotid artery, a major blood vessel in the neck responsible for supplying oxygen-rich blood to the brain. These tumours, often referred to as carotid body tumours or paragangliomas, are typically benign but can cause significant health issues due to their location near vital neurovascular structures. Understanding carotid tumours is crucial because early diagnosis and appropriate management can prevent complications such as stroke, nerve damage, or tumour progression. This article provides a detailed overview of carotid tumours, covering anatomy, causes, symptoms, diagnosis, treatment, and prognosis.

Anatomy / Background

The carotid arteries are paired vessels located on each side of the neck. Each artery bifurcates into the internal carotid artery, which supplies blood to the brain, and the external carotid artery, which supplies the face and scalp. At the bifurcation lies the carotid body, a small cluster of chemoreceptor cells that monitor blood oxygen levels and help regulate respiratory activity.

Carotid tumours most commonly arise from the carotid body and are classified as paragangliomas. These tumours originate from paraganglionic tissue, which is part of the autonomic nervous system. Due to their proximity to critical nerves (such as the vagus and hypoglossal nerves) and blood vessels, carotid tumours can affect neurological function and vascular integrity.

Causes / Etiology

The exact cause of carotid tumours is not fully understood, but several factors are associated with their development:

Symptoms / Clinical Presentation

Carotid tumours often grow slowly and may remain asymptomatic for years. When symptoms do appear, they typically include:

  • Painless, pulsatile neck mass: A slowly enlarging lump near the angle of the jaw that may pulse in time with the heartbeat.
  • Neck discomfort or pain: Due to pressure on surrounding tissues.
  • Dysphagia or hoarseness: If the tumour compresses nearby nerves such as the vagus or hypoglossal nerve.
  • Dizziness or syncope: Rarely, if the tumour affects blood flow or nerve function.
  • Horner’s syndrome: Characterized by drooping eyelid, constricted pupil, and lack of sweating on one side of the face, indicating sympathetic nerve involvement.
  • Tinnitus or hearing changes: If the tumour extends toward the ear.

Diagnosis

Diagnosing carotid tumours involves a combination of clinical examination and imaging studies:

  • Physical examination: Palpation of a firm, mobile, pulsatile mass in the neck that moves side-to-side but not vertically (positive Fontaine’s sign).
  • Ultrasound with Doppler: First-line imaging to assess the vascular nature of the mass and its relationship to the carotid artery.
  • Computed Tomography (CT) scan: Provides detailed anatomical information and helps evaluate tumour size and extent.
  • Magnetic Resonance Imaging (MRI): Offers superior soft tissue contrast and can identify tumour characteristics.
  • Magnetic Resonance Angiography (MRA) or CT Angiography (CTA): Visualizes blood vessels and tumour vascularity.
  • Biopsy: Generally avoided due to risk of bleeding; diagnosis is usually made based on imaging.
  • Genetic testing: Recommended if hereditary paraganglioma syndrome is suspected.

Treatment Options

Treatment depends on tumour size, symptoms, patient health, and potential malignancy:

Procedure Details (Surgical Resection)

Surgical removal of carotid tumours is a delicate procedure performed by experienced vascular or head and neck surgeons:

  1. Preoperative planning: Includes imaging and possible embolization to reduce vascularity.
  2. Anesthesia: General anesthesia is administered.
  3. Incision: A transverse or longitudinal neck incision is made along the anterior border of the sternocleidomastoid muscle.
  4. Exposure: The carotid sheath is carefully opened to expose the carotid artery and tumour.
  5. Tumour dissection: The tumour is meticulously separated from the carotid artery and surrounding nerves, preserving vital structures.
  6. Vascular control: Temporary clamping of the carotid artery may be necessary; vascular reconstruction may be performed if arterial wall involvement occurs.
  7. Hemostasis and closure: Bleeding is controlled, and the incision is closed in layers.

Postoperative Care / Rehabilitation

  • Monitoring: Patients are observed for neurological deficits, bleeding, or airway compromise.
  • Pain management: Analgesics are provided as needed.
  • Physical therapy: May be required if nerve injury affects swallowing or speech.
  • Follow-up imaging: To detect recurrence or complications.
  • Long-term surveillance: Regular clinical and imaging evaluations, especially in hereditary cases.

Risks and Complications

Potential risks associated with carotid tumour and its treatment include:

  • Nerve injury: Leading to hoarseness, swallowing difficulties, or tongue weakness.
  • Stroke: Due to carotid artery manipulation or thrombosis.
  • Bleeding: Intraoperative or postoperative hemorrhage.
  • Infection: At the surgical site.
  • Recurrence: Particularly in hereditary or malignant tumours.
  • Malignant transformation: Rare but possible in some paragangliomas.

Prognosis

Most carotid tumours are benign and have an excellent prognosis when treated appropriately. Surgical resection offers a high cure rate, especially for localized tumours. Malignant carotid paragangliomas are rare but require more aggressive management and have a variable prognosis. Early diagnosis and treatment significantly improve outcomes and reduce the risk of complications.

When to See a Doctor

Seek medical attention if you notice:

  • A new or growing lump in the neck, especially near the jawline.
  • Persistent neck pain or discomfort.
  • Hoarseness, difficulty swallowing, or unexplained neurological symptoms.
  • Pulsatile sensation or bruit over a neck mass.

Early evaluation by a healthcare professional can facilitate timely diagnosis and management.

Conclusion

Carotid tumours, though rare, are important vascular lesions that require careful evaluation due to their proximity to critical neurovascular structures. Understanding their anatomy, causes, symptoms, and treatment options is essential for effective management. Surgical resection remains the cornerstone of treatment, with excellent outcomes in most cases. If you experience any suspicious neck masses or related symptoms, consult a healthcare professional promptly to ensure appropriate care and avoid complications.

Welcome to
Dr Sahaja Vascular Surgeon

Aenean porta orci nam commodo felis hac ridiculus fusce fames maximus erat sed dictumst blandit arcu suspendisse sollicitudin luctus in nec

Make an Appointment.