scholarly journals A rare case of metachronous triple cancers involving the tympanic membrane

2012 ◽  
Vol 29 (1) ◽  
Author(s):  
Hui-Yu Chang ◽  
Hua Jiang ◽  
Fang Zhou
Keyword(s):  
2015 ◽  
Vol 7 (3) ◽  
pp. 141-143
Author(s):  
Hitesh Verma

ABSTRACT The external auditory canal (EAC) is formed by lateral cartilaginous and medial bony part. The stenosis of EAC is narrowing of the width of the EAC, i.e. either caused by congenital or acquired causes. Myringosclerosis is a condition caused by calcification of tissues in the tympanic membrane and ossification is a special form of fibrosis due to the long-term, irreversible continued inflammation in the middle ear cleft. We are presenting rare case of idiopathic tympanic membrane ossification with generalized stenosis of EAC in 29-year-old patient. How to cite this article Verma H, Dass A, Singhal SK, Gupta N. Late Presentation of Idiopathic Tympanic Membrane Ossification with External Auditory Canal Stenosis. Int J Otorhinolaryngol Clin 2015;7(3):141-143.


2018 ◽  
Vol 17 (2) ◽  
pp. 307-310
Author(s):  
Ahmad Hafiz Ali ◽  
Zulkiflee Salahuddin ◽  
Mohd Khairi MD Daud ◽  
Rosdan Salim

Bilateral congenital mesotympanic cholesteatoma is a very rare disease. It can present differently from ordinary congenital cholesteatoma. We report a case of bilateral congenital cholesteatoma diagnosed at age of 22 years old. She presented with bilateral intermittent ear discharge since 10 years old that worsening two weeks prior to her presentation to our clinic and associated with bilateral reduced hearing. Clinically there was intact tympanic membrane with retraction of the mesotympanic area with present of mass medial to tympanic membrane. CT scan imaging showed there was soft tissue in the bilateral middle ear cavity with intact scutum and ossicles. Patient undergone canal wall down procedure and the diagnosis of congenital mesotympanic cholesteatoma was confirmed with present of cholesteatoma sac at the posterosuperior part, as opposed to anterosuperior quadrant, where the common site for congenital cholesteatoma.Bangladesh Journal of Medical Science Vol.17(2) 2018 p.307-310


2010 ◽  
Vol 125 (3) ◽  
pp. 318-320 ◽  
Author(s):  
N de Zoysa ◽  
J Stephens ◽  
G M D Mochloulis ◽  
P B D S Kothari

AbstractObjective:The authors present an extremely rare case of carcinoma of the tympanic membrane.Method:A case report and review of the literature concerning carcinoma of the tympanic membrane and temporal bone are presented and discussed.Results:The authors present a patient with recurrent otorrhoea and an abnormal tympanic membrane. Biopsy was inconclusive, but resection demonstrated squamous cell carcinoma of the tympanic membrane. We also discuss the investigation, diagnosis, natural history and management of this rare condition, as well as the staging and management of tumours of the temporal bone and the differences between these closely related but prognostically different entities.Conclusion:This rare entity can be managed by primary surgical resection if there is no evidence of metastasis.


1986 ◽  
Vol 100 (6) ◽  
pp. 699-700 ◽  
Author(s):  
J. Stage ◽  
T. Vinding

AbstractAn exteremely rare case of traumatic thermal injury of the middle and inner ear with deafness and irreversible peripheral facial palsy is presented. The accident was caused by a metal spark perforating the tympanic membrane during welding.


2011 ◽  
Vol 125 (10) ◽  
pp. 1059-1061 ◽  
Author(s):  
M Sagit ◽  
M Uludag ◽  
I San

AbstractObjective:To report an extremely rare case of dark pigmentation on the tympanic membrane due to alkaptonuria, and to discuss the probable association between this condition and hearing loss.Case report:A 58-year-old man with alkaptonuria was admitted with tinnitus and hearing loss in both ears. Physical examination showed bluish-black pigmentation on the helixes of both ears and both sclerae. Otoscopic examination revealed dark discolouration of both tympanic membranes. Audiological evaluation revealed mixed high frequency hearing loss in both ears. Tympanometric examination revealed type A tympanograms bilaterally, and absence of acoustic reflexes both ipsilaterally and contralaterally. Computed tomography of the temporal bones revealed no abnormality.Conclusion:Clinicians should consider alkaptonuria in the differential diagnosis of patients with abnormal tympanic membrane pigmentation and hearing loss.


2006 ◽  
Vol 120 (9) ◽  
pp. 796-799
Author(s):  
L O Redaelli de Zinis ◽  
C Galtelli ◽  
M G Barezzani

Benign vascular lesions include various forms whose classification has created some controversies in the literature. The observation of a rare case of vascular bulge of the eardrum in a 57-year-old man prompted us to analyse the essential features of these lesions. This was an incidental finding and the mass was removed by a transcanal approach. The patient is free of disease four years later. Vascular malformations can be differentiated from vascular tumours since they are present at birth, are generally stable, do not involute, and do not necessitate treatment unless symptoms occur.


2021 ◽  
Vol 14 (4) ◽  
pp. e241591
Author(s):  
Nurul Asma Che Ab Rahim ◽  
Jeyasakthy Saniasiaya ◽  
Jeyanthi Kulasegarah

High-riding jugular bulb (HRJB), although rare, may pose a challenge as it may be mistaken for other non-alarming condition, such as middle ear effusion. Patients with HRJB classically present with pulsatile tinnitus. We report a unique case of a 26-year-old patient with underlying beta thalassaemia who presented with a 2-month history of intermittent epistaxis and rhinorrhoea. Otoscopic examinations revealed a pulsatile bluish mass behind the right tympanic membrane and a dull left tympanic membrane. Imaging performed revealed a finding of dual retrotympanic pathology, which consisted of a right dehiscent HRJB and left cholesterol granuloma. We highlight a rare case of dual retrotympanic mass as well as its management.


2021 ◽  
Vol 14 (5) ◽  
pp. e241839
Author(s):  
Tobias Engert ◽  
Frank Uwe Metternich

Herniation of the tympanic membrane is a rare benign malformation of the tympanic membrane into the external auditory canal. It may be asymptomatic or associated with symptoms such as aural fullness, tinnitus, otalgia or hearing loss. We present a case of a symptomatic herniation of the tympanic membrane and its surgical therapy with hernia excision and tympanoplasty. An internal review board exemption was obtained.


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