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Retropharyngeal Abscess

A collection of pus in the retropharyngeal space, between the buccopharyngeal fascia covering the constrictor muscles anteriorly and the alar layer of the deep cervical fascia posteriorly. It is predominantly a disease of children under 6 years, and it is an airway emergency.

Anatomy that determines behaviour and danger

  • The retropharyngeal space extends from the skull base to the tracheal bifurcation at approximately the level of T1 to T2, where the alar and visceral fascia fuse. Infection here can descend directly into the superior mediastinum.
  • Posterior to the alar fascia lies the danger space, or space 4, which extends uninterrupted from the skull base to the diaphragm. Infection breaching the alar fascia into this space spreads to the posterior mediastinum with minimal resistance, and this is the anatomical basis of descending necrotising mediastinitis.
  • Retropharyngeal lymph nodes, that is the nodes of Rouvière, drain the nasopharynx, adenoids, posterior paranasal sinuses, middle ear and Eustachian tube. These nodes are prominent in young children and atrophy by around 5 years. Suppurative adenitis of these nodes is the mechanism of retropharyngeal abscess in children, which is why the condition is a paediatric disease and why it declines sharply after the age of 6.
  • In adults, retropharyngeal abscess arises from penetrating trauma including foreign bodies such as fish bones, from instrumentation, from vertebral osteomyelitis, from tuberculosis of the cervical spine producing a cold abscess, and from extension of other deep neck infections. An adult with a retropharyngeal abscess and no obvious source requires investigation for tuberculosis, malignancy, immunodeficiency and an occult foreign body.

Microbiology

Polymicrobial. Streptococcus pyogenes, Staphylococcus aureus including methicillin resistant strains, Streptococcus milleri group, Haemophilus influenzae, and anaerobes including Fusobacterium, Prevotella, Peptostreptococcus and Bacteroides.

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Ménière Disease

An inner ear disorder characterised by recurrent spontaneous vertigo, fluctuating sensorineural hearing loss, tinnitus and aural fullness, associated pathologically with endolymphatic hydrops.

Pathophysiology

Distension of the endolymphatic compartment, most marked in the cochlear duct and saccule, arises from an imbalance between endolymph production and absorption by the endolymphatic sac. The traditional explanation for attacks is rupture of Reissner membrane with potassium rich endolymph entering the perilymphatic space, depolarising and then blocking hair cell and neural function, followed by healing and restoration. This model does not explain all features, and current thinking also implicates altered sac function, immune mechanisms, vascular factors and ion transport abnormality. Endolymphatic hydrops is found in patients without symptoms and is best regarded as a marker rather than the complete explanation.

Diagnostic criteria

Definite Ménière disease requires:

  • Two or more spontaneous episodes of vertigo, each lasting 20 minutes to 12 hours.
  • Audiometrically documented low to mid frequency sensorineural hearing loss in the affected ear on at least one occasion before, during or after an episode.
  • Fluctuating aural symptoms, that is hearing, tinnitus or fullness, in the affected ear.
  • Not better accounted for by another diagnosis.

Probable disease requires episodic vestibular symptoms of 20 minutes to 24 hours with fluctuating aural symptoms, without documented audiometric confirmation.

Natural history

  • Bilateral involvement develops in 25 to 40 percent over 10 to 20 years.
  • Vertigo attacks typically decline in frequency over years and often burn out, while hearing loss progresses and becomes fixed, typically plateauing at 50 to 60 dB with poor discrimination.
  • Tumarkin otolithic crisis, a sudden drop attack without loss of consciousness caused by abrupt otolithic stimulation, occurs in 5 to 10 percent, causes injury, and is an indication for aggressive treatment.

Associations: migraine, which coexists in a substantial proportion and complicates diagnosis; autoimmune disease; and a family history in around 10 percent.