Results 301 to 310 of about 254,564 (326)
Some of the next articles are maybe not open access.
Iatrogenic central retinal artery occlusion after carotid body tumor embolization and excision
GMS Ophthalmology Cases, 2017Objective: To report a case of iatrogenic central retinal artery occlusion after embolization and surgical resection of carotid body paraganglioma. Methods: Case report Results: One adult female patient presented with persistent unilateral visual loss ...
C. M. Rangel+3 more
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The American Journal of Surgery, 1931
Abstract 1. 1. A case of paraganglioma of the carotid body, with symptoms of over a year's duration and with successful surgical removal is reported. 2. 2. Embryology, anatomy, physiology and pathology of the carotid body are briefly discussed. 3. 3.
Rigney D'Aunoy, J.T. Nix
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Abstract 1. 1. A case of paraganglioma of the carotid body, with symptoms of over a year's duration and with successful surgical removal is reported. 2. 2. Embryology, anatomy, physiology and pathology of the carotid body are briefly discussed. 3. 3.
Rigney D'Aunoy, J.T. Nix
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Management of carotid body tumors
Otolaryngologic Clinics of North America, 2001The carotid body tumor is a rare neoplasm that has generated much literature over the past century, and for which continued controversy exists regarding natural history, biologic behavior, proper technique of excision, and the risk of morbidity and mortality. This article discusses overall management of carotid body tumors.
Jari M. van Baalen+2 more
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DeckerMed Vascular and Endovascular Surgery, 2017
Carotid body tumors (CBTs) are derived from parasympathetic autonomic nervous system cells and are the most common type of head and neck paragangliomas, accounting for 65-80% of lesions. CBTs may occur sporadically, may be familial with identified gene mutations on the succinate dehydrogenase subunit, or a component of familial neuroendocrine ...
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Carotid body tumors (CBTs) are derived from parasympathetic autonomic nervous system cells and are the most common type of head and neck paragangliomas, accounting for 65-80% of lesions. CBTs may occur sporadically, may be familial with identified gene mutations on the succinate dehydrogenase subunit, or a component of familial neuroendocrine ...
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Journal of the American Medical Association, 1917
Tumors of the carotid body have great surgical and pathologic interest, but are not of so rare occurrence as they were at one time thought to be. Dr. Scudder 1 of Boston described a case in 1903, which I think was the first case reported in this country; Dr.
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Tumors of the carotid body have great surgical and pathologic interest, but are not of so rare occurrence as they were at one time thought to be. Dr. Scudder 1 of Boston described a case in 1903, which I think was the first case reported in this country; Dr.
openaire +2 more sources
2008
Carotid body tumors are rare neoplasms of the carotid chemoreceptors, which lie in the adventitia of the carotid bifurcation. They may be non-secreting chemodectomas of cells of neural crest origin, or neuropeptide secreting apudomas. Most are sporadic, but 10% are familial, with autosomal dominant inheritance. Bilateral tumors occur in 32% of familial
Paul Srodon, John Lumley
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Carotid body tumors are rare neoplasms of the carotid chemoreceptors, which lie in the adventitia of the carotid bifurcation. They may be non-secreting chemodectomas of cells of neural crest origin, or neuropeptide secreting apudomas. Most are sporadic, but 10% are familial, with autosomal dominant inheritance. Bilateral tumors occur in 32% of familial
Paul Srodon, John Lumley
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Surgical Management of Carotid Body Tumor and Risk Factors of Postoperative Cranial Nerve Injury
World Journal of Surgery, 2020Xiaolang Jiang+7 more
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