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MeSH: nádory kraniálních nervů-diagnóza

11 záznamů v PubMed Filtry

Článek

Das Neurinom des Nervus recurrens
[Neurinoma of the recurrent nerve]

Rozhledy v chirurgii. 2009 Feb ; 88 (2) : 59-61.

Rozhl Chir
ISSN 0035-9351
Zdroj

AIMS: Neurinoma of the recurrent nerve presented a rare diagnosis in thyroid gland surgery. METHODS: A case report is presented and the result of the neurinoma of the recurrent nerve extirpation--nerve paresis--is discussed with the rare results in literature. RESULTS: The preoperative diagnosis is difficult and intraoperative histological diagnosis was not correct. The postoperative paresis of the nerve was clinical only very light. CONCLUSION: The problematical neuromonitoring by isolated nodes in parathyroideal regions and after their exstirpation must lead to the suspicion of a recurrent nerve neurinoma.

MeSH
dospělí MeSH
lidé MeSH
nádory kraniálních nervů komplikace diagnóza chirurgie MeSH
náhodný nález MeSH
nervus laryngeus recurrens * MeSH
neurilemom komplikace diagnóza chirurgie MeSH
ochrnutí hlasivek etiologie MeSH
pooperační komplikace MeSH
Check Tag
dospělí MeSH
lidé MeSH
Publikační typ
anglický abstrakt MeSH
časopisecké články MeSH
kazuistiky MeSH

Článek

Neurofibromatosis 2: two case reports

The international tinnitus journal. 2003 ; 9 (2) : 116-8.

Int Tinnitus J
ISSN 0946-5448
Zdroj

Our study presents two cases of neurofibromatosis 2 (NF2) that have been diagnosed at the Ear, Nose, and Throat Department of Hradec Králové (Czech Republic). The first case involved a young man with a history of sudden hearing loss accompanied by tinnitus on the left side. The diagnosis of NF2 was made, and an operation for left acoustic neuroma was performed. Looking toward the future, the acoustic neuroma on the right side should be resolved as well. The second case concerned a woman (the mother of our patient 1) examined at the same Ear, Nose, and Throat Department in 1980, after 4 years of gait instability and progressive loss of hearing and tinnitus on the right side. Computed tomography scan detected a bilateral expansion in the pontocerebellar angles, and a large tumor on the right side was removed. The patient is deaf and has facial palsy without progression of symptomatology during long-term follow-up. These two cases document the rare but serious hereditary disease of NF2. Its most frequent first presentation is acoustic neuroma; further, benign tumors of the nervous system and juvenile cortical cataract also are often detected. The variability of number, location, and biological behavior of tumors associated with NF2 require an individual patient treatment approach, long-term follow-up, and insertion of appropriate hearing aids. Important also is a genetic examination to exclude pathological NF2 genes in the first-degree relatives of the affected individuals.

Článek

Oculomotor nerve schwannoma

British journal of neurosurgery. 2003 Apr ; 17 (2) : 168-73.

Br J Neurosurg
ISSN 0268-8697
Zdroj

Oculomotor nerve schwannoma is an extremely rare tumour. Only 26 sufficiently described cases of oculomotor nerve schwannomas were found in the literature. The case of an oculomotor nerve schwannoma in a 12-year-old girl is presented. Clinical manifestations, as well as the aim for the radical resection with oculomotor function preservation are reviewed.

MeSH
dítě MeSH
kraniotomie metody MeSH
lidé MeSH
magnetická rezonanční tomografie MeSH
nádory kraniálních nervů diagnóza chirurgie MeSH
nemoci okohybného nervu diagnóza chirurgie MeSH
neurilemom diagnóza chirurgie MeSH
Check Tag
dítě MeSH
lidé MeSH
ženské pohlaví MeSH
Publikační typ
časopisecké články MeSH
kazuistiky MeSH
práce podpořená grantem MeSH
přehledy MeSH

Článek

Our treatment philosophy of gliomas of the anterior visual pathways

Child's nervous system. 1990 Mar ; 6 (2) : 75-8.

Childs Nerv Syst
ISSN 0256-7040
Zdroj

Therapeutic strategy and clinical course of 28 low grade gliomas of the anterior visual tract were analyzed and compared with results of quantitative microscopic examination. Children operated on between 1978 and 1987 were divided into four groups according to the tumor site. DNA microfluorometry and image analysis of bioptic material were used for an objective differentiation between morphologically almost identical gliomas classified as pilocytic astrocytomas (grade I). Six cases of posttraumatic gliosis were examined as controls. Results were tested with factor analysis and by multiple comparison procedures. Significant differences between quantitative parameters of tumors located along the visual pathway were found with the use of computer-aided microscopy. These results corresponded with the clinical experience and patient's outcome. A radical surgical intervention (without additional oncologic therapy) was recommended for patients with intraorbital gliomas which revealed favorable quantitative microscopic features.