Results 151 to 160 of about 1,374 (202)
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Glomus jugulare tumor

The Laryngoscope, 1977
AbstractA review has been made of the current recommendations for treatment of glomus tumors involving the ear. Thirty cases treated in our clinic have been reviewed, comprised of 8 glomus tympanicum and 22 glomus jugulare tumors. We recommend surgical excision as primary treatment for glomus tympanicum tumors and high voltage radiotherapy as primary ...
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Glomus jugulare tumors.

Eye, ear, nose & throat monthly, 1969
To The Editor .—Regarding Dr. H. Rosenwasser's monograph on glomus jugulare tumors in the July 1968Archives. These tumors appear to grow more slowly in the elderly. They may occur in children and are then very malignant and spread rapidly intracranially, involving many cranial nerves, and meningitis may follow when the ear drum is open and infection ...
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Glomus Jugulare Tumors

1982
The first report of a glomus jugulare tumor is attributed to Rosenwasser (1945) with his publication, “Carotid Body Tumor of the Middle Ear and Mastoid.” The true nature of the neoplasm was recognized by the pathologist Otani, but Rosenwasser suggested its origin from the glomus jugularis (sic), recently rediscovered by Guild (1941). Lubbers (1937) was
Frederick G. Zak, William Lawson
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Familial bilateral glomus jugulare tumors

Neuroradiology, 1991
Glomus jugulare tumors may be bilateral or more commonly associated with a glomus tumor in another location. These tumors can also have a familial distribution which appears to be autosomal dominant. In this paper, two brothers are presented with bilateral glomus jugulare tumors. Such occurrence appears to be a unique familial manifestation.
E T, Tali   +4 more
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Metastases of Glomus Jugulare Tumors

Archives of Otolaryngology - Head and Neck Surgery, 1965
Introduction THE GLOMUS JUGULARE, a normal structure first described by Guild, 3 lies in the dome of the jugular bulb just below the floor of the middle ear. The "glomus" is quite small, 0.5 × 0.25 mm, and is composed of nonchromaffin staining paraganglia cells arranged in an organoid pattern.
D M, TAYLOR, B R, ALFORD, S D, GREENBERG
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Radiosurgery for Glomus Jugulare Tumors

Otolaryngologic Clinics of North America, 2009
Glomus jugulare tumors arise from adventitial chemoreceptor tissue in the jugular bulb. Although histologically benign, these tumors can be locally aggressive because of their proximity to the lower cranial nerves and major vascular structures. Traditional treatment involves microsurgical removal with or without endovascular embolization, but morbidity
Jonathan P, Miller   +4 more
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Glomus Jugulare Tumors: Long-Term Tumors

Archives of Otolaryngology - Head and Neck Surgery, 1969
IT HAS become apparent to me and I have said so repeatedly at lectures and in publications, 1,2 that a rational mode of therapy can logically be proposed if one attempts to classify these tumors into stages based on clinical empirical estimation of the underlying pathology, at the time they are first seen.
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Glomus Jugulare Tumor

Otology & Neurotology, 2005
Paul K, Holden, Fred H, Linthicum
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Glomus jugulare tumors

The Laryngoscope, 1952
W L, MATTICK, E M, BURKE
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Glomus Jugulare Tumor (Chemodectoma)

2004
Glomus jugulare tumors have their origin from a small (0.25 to 0.5 mm) group of cells in the adventitia of the jugular bulb. These paraganglia have recently been identified in different places in the petrous bone such as in the tympanic branch of the glossopharyngeal nerve, in the canaliculus tympanicus, and in the submucosa of the promentory.
Michael Salcman   +3 more
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