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Laryngeal carcinoma

Last updated: January 15, 2025

Summarytoggle arrow icon

Laryngeal carcinomas are malignant tumors that arise in the supraglottic, glottic (i.e., involving the vocal cords), and subglottic regions of the larynx. Laryngeal cancers are most commonly squamous cell carcinomas. Smoking and alcohol consumption are the most important risk factors. Glottic cancer is the most common subtype and typically manifests with hoarseness in early stages. Diagnosis is based on tissue biopsy under direct laryngoscopy, and staging is determined via imaging such as CT scan or MRI. Treatment varies based on the site and stage of the tumor. Early-stage cancers are usually treated with radiation therapy or transoral laser microsurgery with the goal of voice preservation. Advanced stages often require laryngectomy. Patients with supraglottic or subglottic cancer often present later than those with glottic cancer, which typically results in a poorer prognosis. Vocal rehabilitation is indicated after laryngectomy to help patients regain speech production.

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Epidemiologytoggle arrow icon

  • Sex: >
  • Age of onset: 40–70 years

References:[1]

Epidemiological data refers to the US, unless otherwise specified.

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Etiologytoggle arrow icon

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Classificationtoggle arrow icon

Laryngeal carcinomas are classified according to their location in relation to the glottis.

Laryngeal carcinomas are almost always squamous cell cancers (SCC)!

References:[4]

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Clinical featurestoggle arrow icon

Unexplained hoarseness for longer than 3 weeks should always be investigated by laryngoscopy!

References:[5]

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Diagnosistoggle arrow icon

Initial workup [2][6]

Patients with clinically suspected laryngeal cancer should be promptly referred to otolaryngology.

Further workup [7]

Order staging imaging if malignancy is confirmed.

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Differential diagnosestoggle arrow icon

The differential diagnoses listed here are not exhaustive.

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Treatmenttoggle arrow icon

General principles [2]

  • Individualize treatment in consultation with a multidisciplinary tumor board.
  • Obtain pretreatment evaluations from a speech pathologist, dietitian, and, if radiation therapy is planned, a dental specialist.
  • Treatment is based on tumor location and stage, comorbidities, performance status, and goals of care.
  • After treatment, regularly monitor for recurrence.

A patient with laryngeal carcinoma is at risk for airway obstruction. See “Airway management in head and neck cancer” before procedural sedation and/or airway manipulation.

Treatment modalities [2]

Management includes one or more of the following options:

Larynx-preservation techniques should be preferred if appropriate.

Posttreatment voice rehabilitation [2]

Voice rehabilitation is used to help patients regain speech production after laryngectomy.

  • Tracheoesophageal prosthesis (e.g., Blom-Singer valve)
  • Alternative options
    • Esophageal speech: an alternative method of speaking that involves swallowing air and directing it into the upper esophagus
    • Electrolarynx: a device that, when pressed against the soft tissue of the throat, produces pharyngeal vibrations to allow speech production

Posttreatment monitoring [8]

After radiation therapy, measure TSH levels every 6–12 months to assess for radiation-induced thyroid dysfunction. [8]

Management of recurrence [10]

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Prognosistoggle arrow icon

  • Five-year survival rates after initial diagnosis of laryngeal cancer vary by disease stage. [11]
    • Overall (all stages): ∼ 62%
    • Localized disease (no spread): ∼ 79%
    • Regional disease (spread to lymph nodes): ∼ 48%
    • Distant disease (metastatic): ∼ 34%
  • Five-year overall survival rates also vary greatly by site. [9]
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