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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 Miller   +2 more
exaly   +3 more sources

Glomus jugulare tumor

Postgraduate Medicine, 1982
A 53-year-old woman with left vocal cord paralysis was seen for sharp shooting pains in the left side of the neck and the left shoulder and upper arm. Glomus jugulare tumor was diagnosed, based on clinical findings and results of angiography and computed tomography. Because surgery was contraindicated, radiotherapy was used.
M R, Swenson, W, Sibley
openaire   +2 more sources

Glomus Jugulare Tumor

JAMA: The Journal of the American Medical Association, 1969
ABSTRACT To the Editor:— I agree with the comments by Dr. Raymond Schiffman. The term "glomus jugulare tumor" (or nonchromaffin paraganglioma of glomus jugulare; or chemodectoma of glomus jugulare) obviously cannot apply to histologically similar tumors which do not arise from the normal structure which bears that name.
openaire   +4 more sources

Chemodectomas of the glomus jugulare

Cancer, 1972
Chemodectomas of the glomus jugulare are best controlled by a combined approach where radical mastoidectomy is followed by 4500 rads external megavoltage irradiation. Postoperative radiotherapy both delays recurrences (by an average of 10 years) and reduces the frequency of recurrences.
P M, Hatfield, A E, James, M D, Schulz
openaire   +2 more sources

Glomus Jugulare and Vagale

Annals of Otology, Rhinology & Laryngology, 1978
The therapeutic results in 72 patients with glomus jugulare and nine with glomus vagale have indicated a surgical cure rate of 80% in the former and 100% in the latter. Radiotherapy demonstrated a 65% tumor response rate and a 25% cure rate histologically and clinically.
J H, Ogura, G J, Spector, M, Gado
openaire   +2 more sources

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 ...
openaire   +2 more sources

Tumors of the glomus jugulare and glomus tympanicum

Cancer, 1966
Seven patients with tumors of the glomus jugulare and/or glomus tympanicum —6 treated initially by radical endaural mastoidectomy and one by simple excision—are presented. Clinical, pathologic and therapeutic data are compared with cases in the world literature.
K L, Schermer   +3 more
openaire   +2 more sources

Glomus Jugulare Tumors

Archives of Otolaryngology - Head and Neck Surgery, 1957
Although glomus jugulare tumor is not very common, it is still sufficiently prevalent not to be considered among those that are rarely encountered. As additional attention is given to this disease, more cases will be uncovered. This is evidenced by the marked increase in the number of cases reported ever since the first report made by Rosenwasser, in ...
openaire   +2 more sources

TUMORS OF THE GLOMUS JUGULARE NOT ASSOCIATED WITH THE JUGULAR VEIN

Archives of Otolaryngology - Head and Neck Surgery, 1951
DURING the past six years the term glomus jugulare has been employed with increasing frequency to designate certain tumors of the middle ear arising from small vascular bodies normally found in the adventitia of the jugular vein near the ramus tympanicus of the ninth cranial nerve.
T, WINSHIP, J, LOUZAN
openaire   +2 more sources

Ultrastructure of the Glomus Jugulare Tumor

Archives of Otolaryngology - Head and Neck Surgery, 1968
THE GLOMUS JUGULARE is considered as one of the nonchromaffin paraganglia. It is found as small conglomerates of cells in the dome of the jugular bulb, or along the fossa jugulare in the nerve of Jacobson, or in the nerve of Arnold.1It was first described by Guild in 1941, who was impressed by the similarity of the structure of this organ with that of ...
A, González-Angulo   +3 more
openaire   +2 more sources

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