Results 41 to 50 of about 1,311 (203)
Jugular paraganglioma treatment at the UMC Maribor
Zdravniški Vestnik, 2017 Background: Jugular paragangliomas are rare, almost exclusively benign and slowly growing tumors. Arising from the cells of paraganglia in jugular bulb, they infiltrate the temporal bone and later grow intracranially.
Janez Rebol +4 more
doaj +1 more source
Recurrent glomangioma (“true” glomus tumor) of the middle ear and mastoid
World Journal of Otorhinolaryngology - Head and Neck Surgery, Volume 5, Issue 4, Page 175-179, December 2019., 2019 Objective To review current literature and experience with glomangiomas, or true glomus tumors of the middle ear and mastoid as well asto report on the exceptionally rare case of a glomangiomastemming from the middle ear space with multiple recurrences.
Adam C. Kaufman +4 more
wiley +1 more source
Case report of glomus jugulare tumour associated with a posterior fossa cyst
, 2009 A subgroup of complex glomus jugulare tumours exists. This includes: multiple, giant or neuropeptide-secreting lesions; those associated with other lesions, such as dural arterio-venous malformation or an adrenal tumour; and tumours in which there has ...
Milford, Chris A. +3 more
core +1 more source
Malignant Potential of Temporal Bone Paragangliomas With Reference to GAPP System
Laryngoscope Investigative Otolaryngology, Volume 11, Issue 2, April 2026.ABSTRACT Objectives To evaluate the temporal bone paragangliomas (so‐called glomus tumors, TB‐PGLs) via the Grading System for Adrenal Pheochromocytoma and Paraganglioma (GAPP) and succinate dehydrogenase subunit B (SDHB) immunohistochemistry, and to discuss their implications for postoperative follow‐up and treatment strategies. Methods This report is
Noritaka Komune +10 more
wiley +1 more source
An unusual case of simultaneous left glomus vagale, jugulare and tympanicum tumor
The Pan African Medical Journal, 2017 A 49-year-old male who attended our hospital due to a history of left hearing loss over a period of 2 years, associated to otalgia, and vertigo to which bleeding in the left ear and facial paralysis had been added in the last 4 months.
Salah Bellasri, Mounir Hmidi
doaj +1 more source
Laryngoscope Investigative Otolaryngology, Volume 10, Issue 4, August 2025.Patients with jugular foramen tumors may have sensorineural hearing loss unrelated to direct cochlear or 8th nerve involvement. Cochlear implantation can be employed to rehabilitate hearing in this setting. ABSTRACT Introduction Cochlear implantation (CI) may be used as a viable method for restoring hearing in patients with sensorineural hearing loss ...
Nicole Ewer +5 more
wiley +1 more source
A Small Glomus Tympanicum Tumor Resected by Minimally Invasive Transcanal Endoscopic Approach
Case Reports in Otolaryngology, Volume 2019, Issue 1, 2019., 2019 We present a case of the transcanal endoscopic resection of a glomus tympanicum tumor. A 51‐year‐old woman presented with pulsatile tinnitus of the right ear persisting for 6 months. A reddish mass was observed through her tympanic membrane. A computed tomography scan revealed a small mass in the mesotympanum.
Masafumi Ohki +2 more
wiley +1 more source
Xiehe Yixue Zazhi, 2021 Objective To summarize the key points of the operation related to the facial nerve function after surgery of paraganglioma involving the jugular foramen in the lateral skull base.
ZHANG Liqin +4 more
doaj +1 more source
Journal of Veterinary Internal Medicine, Volume 39, Issue 3, May/June 2025.ABSTRACT Background Jugular foramen syndrome (JFS), dysfunction of cranial nerves (CNs) IX, X, and XI caused by lesions involving the jugular foramen (JF), is rarely reported in dogs. Objective Describe presenting complaints, neurologic findings, advanced imaging findings, underlying diagnoses, and outcomes in dogs with JFS.
Megan Madden +7 more
wiley +1 more source
A Unique Case of an Aggressive Gangliocytic Paraganglioma of the Filum Terminale
Case Reports in Surgery, Volume 2016, Issue 1, 2016., 2016 Paragangliomas are rare neuroendocrine tumors that are mostly found in the head and neck. Even less common are gangliocytic variant paragangliomas of the spine for which there are only 7 other documented cases in the literature. We report a case of gangliocytic paraganglioma of the sacral spine in a 68‐year‐old man.
Omar S. Akbik +5 more
wiley +1 more source