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Collet–Sicard syndrome (CSS) refers to the unilateral lesion of cranial nerves IX to XII. The cause in this case is spontaneous dissection of the internal carotid artery (ICA), for which multidetector-row computed tomography (MDCT) images were critical for diagnosis.
CASE REPORT
A 54-year-old man noticed an onset of headache, hoarse voice and swallowing compromise. Neurological examination disclosed left-sided palsies of cranial nerves IX to XII.
MDCT demonstrated coiling of the cervical distal portion of left ICA (fig 1A), narrowed lumen, mural thickening, increased external diameter and a thin annular ring of enhancement (“target appearance”)1 (fig 1A, B). Signs of nerve dysfunction were also noticed (fig 2).
Axial T1-weighted magnetic resonance images confirmed the dissection (fig 1C).
DISCUSSION
Causes of CSS include skull-base tumours and fractures, ICA dissection and vasculitis.2 Near their points of exit, the lower nerves (IX to XII) lie in a narrow space even in normal conditions,3 so any adjacent lesion can cause compression.
The role of CT in the diagnosis of ICA dissection has evolved. Early studies demonstrated arterial wall thickening,4 5 but MDCT modified the scenario.
MDCT, in this case, was able to provide assessment not only of ICA dissection itself, but also of the effects of lower cranial nerve palsies (corroborating neurological examination), all obtained in a single sitting. Knowledge of all the diagnostic possibilities included in a single MDCT study is of paramount importance, as MDCT can be an adequate alternative to MRI in specific clinical settings or in a resource-limited environment.
Acknowledgments
This article has been adapted from Lucato L T, Passos R B D, Campos C R, Conforto A B, McKinney A M. Multidetector-row computed tomography in the diagnosis of Collet–Sicard syndrome Journal of Neurology, Neurosurgery and Psychiatry 2008;79:521
Footnotes
Competing interests: None.