Skull base osteomyelitis: A rare entity

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Presentation transcript:

Skull base osteomyelitis: A rare entity Stipe Ivančić, MD1 Klaudija Višković, MD, PhD2 Bruno Baršić, MD, PhD, Professor2 Vladimir Krajinović, MD, PhD2   1Emergency Medicine Institute of Varaždin County, Varaždin, Croatia. 2University Hospital for Infectious Diseases “Fran Mihaljević”, Mirogojska cesta 8, Zagreb, Croatia.

History A 63-year old man with a previously operated cholesteatoma was admitted to the hospital with symptoms of vomiting and vertigo. Symptoms progressed despite receiving coamoxiclav, cranial nerve palsies appeared and patient was transferred to the ICU because of respiratory failure. Results of hemocultures (P. aeruginosa positive) narrowed therapy to meropenem and cefepim.

During hospitalization patient suffered a massive ischemic stroke (Fig During hospitalization patient suffered a massive ischemic stroke (Fig. 1) because of compression of the left internal carotid artery (Fig. 2). The patient died due to complications and spread of infection. Fig. 1 Fig. 2

Cranial CT is usually used as the initial diagnostic test, though its sensitivity in detecting disease is fairly limited without intial bone destruction. MRI on the other hand can differentiate between the soft tissue structures, but cannot differentiate between multiple disease processes (Fig. 3). Fig. 3

Central skull base osteomyelitis Central skull base osteomyelitis is an infection localized to the sphenoid and temporal bones. It occurs as a complication of malignant otitis externa and/or media. The most frequent causative pathogen is Pseudomonas aeruginosa. Risk factors include old age and diabetes. Patients usually present with symptoms of headache and cranial nerve palsies. Therapy should be directed at P. aureginosa with a combination of ceftazidime and carbapenem for a mininum of 6 weeks.