2000
DOI: 10.1258/0022215001903771
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Schwannoma of the chorda tympani nerve

Abstract: We report a case of schwannoma of the chorda tympani. This is a very rare benign tumour and only five other cases have been found in the literature. This is the first case to mimic a cholesteatoma presenting as a pearly tumour in the postero-superior segment of the drum with aural discharge and conductive deafness. Diagnosis is usually by biopsy and treatment is surgical with preservation of facial and auditory function. A summary of the other presentations of this tumour together with a review of the histopat… Show more

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Cited by 21 publications
(20 citation statements)
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“…Depending on the size and location of the tumour, there may exist hearing loss, as reported in 10 previous cases [2][3][4][5][6][7][8][9][10][11] and in our patient (Table 1). Interestingly, seven patients showed a mass in the external ear canal [3][4][5][6][7][8]10] . Only two cases were associated with neurofibromatosis [2,14] .…”
Section: Discussionsupporting
confidence: 70%
See 1 more Smart Citation
“…Depending on the size and location of the tumour, there may exist hearing loss, as reported in 10 previous cases [2][3][4][5][6][7][8][9][10][11] and in our patient (Table 1). Interestingly, seven patients showed a mass in the external ear canal [3][4][5][6][7][8]10] . Only two cases were associated with neurofibromatosis [2,14] .…”
Section: Discussionsupporting
confidence: 70%
“…Only one of the previously published cases employed these methods [7] . It is remarkable that the terminology is often confusing.…”
Section: Discussionmentioning
confidence: 99%
“…The main complaint seen in the papers studies [3][4][5] was hearing loss; there were also ear fullness, otorrhea and otalgia; we stress the absence of paralysis or facial nerve paresis in all the cases. Our patient also came to us because of hearing loss and otalgia.…”
Section: Discussionmentioning
confidence: 84%
“…Ambos exámenes son complementarios para planificar la cirugía y permitir una resección completa y segura del tumor 1 . Histológicamente son tumores caracterizados por un crecimiento fusiforme con áreas Antoni A y B alternantes, con S-100 positivo en la inmunohistoquímica [5][6] . El objetivo del tratamiento en los pacientes con SNF debe intentar preservar la función del nervio facial por el mayor tiempo posible.…”
Section: Discussionunclassified