2018
DOI: 10.11152/mu-1199
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Case report of a rare glomus jugulare tumor extended within the extracranial internal jugular vein: emphasis on initial ultrasound findings and literature review

Abstract: Glomus jugulare tumor (GJT) is a rare benign neoplasm that is located in the skull base; it is impossible for ultrasonography to detect it in most cases. In this article, we present the case of a rare giant GJT, which extended into the internal jugular vein in the neck, initially detected by ultrasonography and confirmed by MRI and pathology. We highlight the initial ultrasonography findings and review the literature to summarize the ultrasonographic features of GJT.

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Cited by 6 publications
(4 citation statements)
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“…Moreover, residual or recurrent tumors are not rare, which may require the further treatments. Currently various treatment options, including surgery, radiation therapy and endovascular procedures were reported [3][4][5].…”
Section: Discussionmentioning
confidence: 99%
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“…Moreover, residual or recurrent tumors are not rare, which may require the further treatments. Currently various treatment options, including surgery, radiation therapy and endovascular procedures were reported [3][4][5].…”
Section: Discussionmentioning
confidence: 99%
“…Our two cases responded to radiosurgery nicely, and the tumors showed a remarkable shrinkage or standstill of growth without causing any symptomatic deterioration. Since one case still have residual and untreated tumor outside the cranium [5], he may require an additional treatment later on. Since the glomus jugulare tumors are large or huge when they are found, or even after microsurgery, they cannot be managed by only one procedure.…”
Section: Discussionmentioning
confidence: 99%
“…Radiological imaging techniques, especially magnetic resonance imaging (MRI), are the major methods for the diagnosis of glomus juglare tumor. There are very few reports of ultrasound in the diagnosis of glomus juglare being located in the skull base 3 .…”
Section: Discussionmentioning
confidence: 99%
“…The classic adrenal origin pheochromocytoma is catecholamine producing paragangliomas arising in the adrenal medulla. Although, majority of these nonadrenal tumors are non-secretory, catecholamine producing paragangliomas of the head and neck 3 .…”
Section: Introductionmentioning
confidence: 99%