Bilateral Peritonsillar Abscess in a Secondary Health Facility in North-Western Nigeria: A Case Series of Two Patients

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ID: 314179
2026
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Abstract
A peritonsillar abscess (PTA) is a localized collection of pus in the space between the tonsillar capsule and the superior constrictor muscle. It is the most common infection of the deep neck spaces. Bilateral PTA (BPTA) is rare and may mimic the symptoms of acute tonsillitis, often leading to delayed diagnosis. Treatment options include needle aspiration, incision and drainage, and quinsy tonsillectomy. The first case involved a 16-year-old girl who presented with a 1-week history of progressively worsening sore throat, odynophagia, persistent fever, and bilateral earache but no respiratory difficulty. On examination, she was in painful distress, dehydrated, febrile, and not pale. She had bilateral tender jugulodigastric lymphadenopathy, mild trismus, enlarged hyperemic kissing tonsils, inflamed peritonsillar regions, and a centrally positioned but edematous uvula. Bilateral needle aspiration yielded pus, and she responds well to antibiotics and supportive treatment. The second case was a 13-year-old boy who presented with an 8-day history of progressive throat pain, dysphagia, fever, bilateral referred otalgia, difficulty in mouth opening, and a change in voice, but no respiratory distress. He appeared in painful distress, febrile, dehydrated, with a “hot potato” voice and moderate to severe trismus. Attempts to further examine the oropharynx and aspirate the pus were not successful due to severe trismus. He underwent a quinsy tonsillectomy and responded well to broad-spectrum antibiotics. In conclusion, BPTA is uncommon and requires a high index of suspicion for prompt diagnosis and timely management to prevent life-threatening complications.
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2026bilateral1 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Lawal Shu’aibu, Abdullahi Adamu, Sani Dandela
Journal Yemen Journal of Medicine
Year 2026
DOI
10.63475/yjm.v5i1.0308
URL
Keywords Keywords not found

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