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chondroblastoma/gluhoća
Veza se sprema u međuspremnik
11 rezultati
Temporal bone chondroblastoma: a review.
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The objective of this paper was to review temporal bone chondroblastomas in regard to their presentation, radiographic findings, histopathology, and treatment. A case report of a 38-year-old man who presented with the left-sided hearing impairment and temporal swelling was reviewed. A CT scan
Temporal bone chondroblastoma: systematic review of clinical features and outcomes
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Objectives: Chondroblastoma is an uncommon benign neoplasm of cartilaginous origin usually involving the long bones. The temporal bone is a rare location for this tumor. As such, the clinical profile, optimal medical and surgical
Benign chondroblastoma of the temporal bone.
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Benign chondroblastoma is a rare tumor in the temporal bone. It occurs preponderantly in middle-aged men as a mass in the postero-superior region of the ear canal and is accompanied by hearing loss. On pathologic examination, giant cells and focal regions of chondroid differentiation are noted.
Lateral skull base chondroblastoma resected with facial nerve posterior transposition.
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BACKGROUND
Chondroblastoma is a rare tumor that can involve the temporal bone. Because it is a benign tumor, functional surgery must be proposed. We report a case of a patient with a massive chondroblastoma operated on with preservation of the facial nerve, and description of the surgical
Temporal bone chondroblastomas.
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OBJECTIVE
To review temporal bone chondroblastomas in regards to their presentation, radiographic findings, histopathology, and treatment.Study design Case report and literature review.
METHODS
A case report of a 38-year-old man is reviewed who presented with left-sided mixed hearing loss, otalgia,
Chondroblastoma of the apex portion of petrousal bone.
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BACKGROUND
Skull chondroblastoma is extremely rare. We described in this study the first case of petrousal bone apex chondroblastoma.
METHODS
The tumor occurred in a 12-year-old girl and was revealed by left hypoacusis, vertigo, and walking instability. Computerized tomography scan depicted
[A case of chondroblastoma arising from the temporal bone].
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A 33-year-old male sustained hearing disturbance in the left ear that exacerbated over a period of three years. The patient was referred to the department of otorhynolaryngology for severe stenosis of the left external auditory canal, where neuroimaging study revealed a huge tumor in the left
Chondroblastoma of the temporal bone.
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Chondroblastomas are highly destructive tumors that are derived from immature cartilage cells. The occurrence of this tumor in the temporal bone or skull base is uncommon. Approximately 70 cases have previously been reported, several of which have involved the temporomandibular joint (TMJ). We
Temporal Bone Chondroblastoma: a Rare Entity
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Introduction: Chondroblastoma is an uncommon benign, locally destructive tumor that usually arises from epiphyses of the long bones. Temporal bone chondroblastoma is an extremely rare occurrence. Chondroblastoma arise from immature
Functional treatment of temporal bone chondroblastoma: retrospective analysis of 3 cases
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Purpose: To describe and analyse functional treatment of temporal bone chondroblastoma (TBCh).
Methods: From January 2000 to June 2019, at the Department of
Successful function-preserving therapy for chondroblastoma of the temporal bone involving the temporomandibular joint.
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We present a case involving a late diagnosis of chondroblastoma of the temporal skull base involving the temporomandibular joint (TMJ). Following an initial misdiagnosis and unsuccessful treatment over a period of 5 years, the patient was referred to our department for further evaluation and
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