AI Article Synopsis

  • Gradenigo syndrome (GS) is a rare complication of severe ear infections characterized by abducens nerve palsy, retro-orbital pain, and ear discharge (otorrhea).
  • A case study describes a 15-year-old male who developed GS after left otitis media, showing symptoms like fever, diplopia (double vision), and severe headaches, with imaging revealing serious underlying issues.
  • Treatment involved intravenous antibiotics and anticoagulants, which led to symptom improvement, highlighting the importance of timely diagnosis and intervention to avoid complications.

Article Abstract

Gradenigo syndrome (GS) is characterized by a triad of clinical features: abducens nerve palsy, retro-orbital pain, and otorrhea, arising as a complication of suppurative otitis media. Herein, we present a case of GS in a 15-year-old male patient, secondary to left otitis media. The patient exhibited fever, otorrhea, accompanied by diplopia, retrobulbar pain, and headache. Imaging studies demonstrated petrous bone destruction and inflammatory changes with opacification of petrous bone, mastoid cells and surrounding structures, confirming the diagnosis of GS. Treatment included intravenous antibiotics and anticoagulants, resulting in the resolution of symptoms and radiological improvement. GS, though rare, warrants prompt recognition and appropriate management to prevent severe complications. Diagnostic imaging plays a crucial role in evaluation, and treatment often involves prolonged antibiotic therapy and, in severe cases, surgical intervention. Understanding the clinical presentation and management strategies is essential for clinicians encountering this condition.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11403888PMC
http://dx.doi.org/10.1016/j.radcr.2024.08.002DOI Listing

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