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Glomangiosarcoma is a low grade [1] tumor of the soft tissue. They rarely metastasize, [2] but metastases are possible. [3] It is also known as malignant glomus tumor. [4] Positive staining for vimentin has been reported. [5]
A glomus tumor (also known as a "solitary glomus tumor" [1]) is a rare neoplasm arising from the glomus body and mainly found under the nail, on the fingertip or in the foot. [2]: 670 They account for less than 2% of all soft tissue tumors. [3] The majority of glomus tumors are benign, but they can also show malignant features. [4]
Glomus tympanicum and Glomus jugulare, also known as jugulotympanic paraganglioma: Both commonly present as a middle ear mass resulting in tinnitus (in 80%) and hearing loss (in 60%). The cranial nerves of the jugular foramen may be compressed, resulting swallowing difficulty, or ipsilateral weakness of the upper trapezius and ...
glomus tumor: Relief of pain at tumor site upon vascular occlusion of limb, with acute return of pain on reperfusion Hippocratic face: Hippocrates: palliative care: impending death: Hippocratic fingers: Hippocrates: pulmonary medicine: chronic hypoxia: clubbing of distal phalanges Hirschberg test: Julius Hirschberg: ophthalmology: strabismus
M8690/1 Glomus jugulare tumor, NOS (C75.5) Jugular/jugulotympanic paranglioma; M8691/1 Aortic body tumor (C75.5) Aortic/aorticopulmonary paraganglioma; M8692/1 Carotid body tumor/paraganglioma (C75.4) M8693/1 Extra-adrenal paraganglioma, NOS Nonchromaffin paraganglioma, NOS; Chemodectoma; M8693/3 Extra-adrenal paraganglioma, malignant
Glomus jugulare tumor: A glomus jugulare tumor is a tumor of the part of the temporal bone in the skull that involves the middle and inner ear structures. This tumor can affect the ear, upper neck, base of the skull, and the surrounding blood vessels and nerves. A glomus jugulare tumor grows in the temporal bone of the skull, in an area called ...
Tumors of the paraganglionic tissues are known as paragangliomas, though this term tends to imply the nonchromaffin type, and can occur at a number of sites throughout the body. Chromaffin paragangliomas are issued from chromaffin cells, and are known as pheochromocytomas .
Hildreth's sign is a physical examination technique useful in differentiating glomus tumors and hemangiopericytomas from other masses with a similar appearance. It was first described by DH Hildreth, in 1970. [1]