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Describe olfaction and the disorders of smell.

ENT · 3rd Professional

Physiology of Olfaction

  • Olfaction is mediated by the olfactory epithelium, a small patch of specialised neuroepithelium (2 to 5 cm² each side) in the roof of the nose, the upper septum and the superior turbinate.
  • It is the only place in the body where neurones are directly exposed to the external environment.
  • The olfactory neurones regenerate throughout life from basal cells, which is unique in the nervous system and is why post-viral anosmia may recover over months — and why patients should not be told the loss is necessarily permanent

Disorders of Smell

  • Terminology — anosmia (complete loss); hyposmia (reduced); parosmia (a distorted perception of a real odour, unpleasant); phantosmia (perception without a stimulus, a hallucination); and cacosmia (perception of a foul smell, often from a real local source)
  • The causes divide into three mechanisms.
  • 1. Conductive (transport) loss — odorant cannot reach the olfactory cleft: nasal polyps, chronic rhinosinusitis, allergic rhinitis, severe septal deviation, tumour, and mucosal oedema. These are the treatable causes, and the loss is often fully reversible
  • 2. Sensorineural loss — damage to the epithelium or the nerve: post-viral (a leading cause, classically after influenza and prominently after COVID-19); head injury, in which the fibres are sheared as they cross the cribriform plate, after an occipital blow, and which is permanent; toxins and drugs; and ageing
  • 3. Central — parkinson and alzheimer disease, in both of which anosmia may precede the motor or cognitive features by years and is an early marker; frontal lobe or olfactory groove meningioma, which may present with foster kennedy syndrome; temporal lobe epilepsy, in which an olfactory aura (uncinate fit) occurs; and multiple sclerosis
  • Kallmann syndrome — congenital anosmia with hypogonadotrophic hypogonadism, from failed migration of the olfactory and GnRH neurones.
  • Assessment — establish onset (sudden or gradual), preceding illness or injury, and unilateral or bilateral; a full nasal examination with endoscopy to see the olfactory cleft specifically; and formal smell testing (UPSIT, Sniffin’ Sticks).
  • Imaging — CT for sinonasal disease, and MRI where a central cause is suspected, particularly with unilateral loss, phantosmia or neurological signs
  • Management — treat the conductive causes.
  • Olfactory training — repeated sniffing of four distinct odours (classically rose, eucalyptus, lemon and clove) twice daily for months — has reasonable evidence in post-viral and post-traumatic loss and is cheap, safe and the only intervention for sensorineural loss

All questions in Anatomy and Physiology of the Nose and Paranasal Sinuses

  1. Q1Describe the anatomy of the nasal cavity and its lateral wall. ★
  2. Q2Describe the paranasal sinuses and the osteomeatal complex. ★
  3. Q3Describe the blood supply and nerve supply of the nose. ★
  4. Q4Describe the physiology of the nose. ★
  5. Q5Describe the clinical examination and investigation of the nose and paranasal sinuses. ★
  6. SN1Describe the nasal septum with its pathology and surgery. ★
  7. SN2Describe mucociliary clearance and its disorders. ★
  8. SN3Describe olfaction and the disorders of smell. ★
  9. SN4Describe the development of the nose and its congenital anomalies. ★
  10. SN5Describe the anatomy and clinical importance of the nasopharynx. ★
  11. SN6Describe the endoscopic anatomy of the nose and the landmarks of safe sinus surgery. ★
  12. SN7Describe the turbinates, turbinate hypertrophy and atrophic rhinitis.

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