2018
DOI: 10.1016/j.radcr.2017.09.020
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Hyperacute unilateral contrast-induced parotiditis during cerebral angiography

Abstract: An uncommon complication of iodinated contrast administration is the development of bilateral sialadenitis. We report a unique case of hyperacute unilateral parotiditis during diagnostic cerebral angiography of the external carotid artery, which mimicked possible iatrogenic vascular event associated with cerebral endovascular procedures. Discussion includes the differential diagnosis, diagnostic studies, and treatments for this unusual condition.

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Cited by 3 publications
(2 citation statements)
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“…Originally thought to be IgE-mediated, the swelling symptoms have been mistakenly attributed to angioedema or anaphylaxis (19). While the exact pathogenesis of iodine mumps is still unclear, the current understanding of the condition is a pseudoallergic reaction to contrast related to accumulation of iodine in the salivary gland ducts (28,38,64). The concentration of iodine in the salivary gland has been measured up to 100 times plasma level and may be exacerbated by renal injury causing impaired iodine excretion (3,64).…”
Section: Introductionmentioning
confidence: 99%
“…Originally thought to be IgE-mediated, the swelling symptoms have been mistakenly attributed to angioedema or anaphylaxis (19). While the exact pathogenesis of iodine mumps is still unclear, the current understanding of the condition is a pseudoallergic reaction to contrast related to accumulation of iodine in the salivary gland ducts (28,38,64). The concentration of iodine in the salivary gland has been measured up to 100 times plasma level and may be exacerbated by renal injury causing impaired iodine excretion (3,64).…”
Section: Introductionmentioning
confidence: 99%
“…CIS manifests as a painless bilateral symmetric salivary gland edema probably due to the accumulation of iodine within the glands, causing a local inflammatory process [2] . It can appear within minutes after ICM administration of until 5 days [3 , 4] . Since the first case described in 1956 by J. Miller et al.…”
Section: Introductionmentioning
confidence: 99%