Extranasopharyngeal Angiofibroma from the Nasal Septum: A Case Report and a Minireview

2010 ◽  
Vol 3 (3) ◽  
pp. 169-171 ◽  
Author(s):  
PP Singh ◽  
Neelima Gupta ◽  
Lakshmi Vaid ◽  
Neeru Chugh
Keyword(s):  
Case Report ◽  
Nasal Septum ◽  
World Literature ◽  
Sphenoid Sinus ◽  
Infratemporal Fossa ◽  
Middle Turbinate ◽  
Inferior Turbinate ◽  
Ethmoid Sinus ◽  
The World ◽  
Extranasopharyngeal Angiofibroma

Abstract Extranasopharyngeal angiofibromas are rare tumors with only 65 cases being reported in the world literature. The most common sites involved are maxillary sinus, ethmoid sinus, sphenoid sinus, nasal septum, middle turbinate, inferior turbinate, cheek, conjunctiva, pterygomaxillary fissure, infratemporal fossa and laryngotracheal tree. We report on a case of 18 years old male patient of extranasopharyngeal angiofibroma of nasal septum.

Polyps originating from accessory middle turbinate and secondary middle turbinate

2012 ◽  
Vol 126 (7) ◽  
pp. 729-732 ◽  
Author(s):  
H Jung ◽  
S K Park ◽  
J-R Kim
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
World Literature ◽  
Middle Turbinate ◽  
Anatomical Variations ◽  
Sinus Surgery ◽  
Histopathological Analysis ◽  
Middle Meatus ◽  
The World ◽  
Paranasal Sinus Computed Tomography

AbstractObjective:We report two extremely rare cases of polyps from unilateral accessory middle turbinates, one of which coexisted with a polyp from an inferomedially projecting, pneumatised, secondary middle turbinate.Methods:Case report and literature review concerning accessory middle turbinate and secondary middle turbinate.Results:Two patients presented with unilateral nasal obstruction. In both patients, nasal endoscopy revealed polypoid masses originating from the middle meatus. Paranasal sinus computed tomography and histopathological analysis confirmed the presence of polyps originating from an accessory middle turbinate and secondary middle turbinate, which were resected uneventfully via endoscopic sinus surgery.Conclusion:To our knowledge, this is the first report in the world literature of polyps originating from a unilateral accessory middle turbinate and secondary middle turbinate. Pre-operative recognition of these rare anatomical variations is of particular importance in avoiding intra-operative complication.

Sialadenoma papilliferum of nasal cavity: case report

2008 ◽  
Vol 122 (9) ◽  
Author(s):  
H E Ozel ◽  
G Ergul ◽  
O E Gur ◽  
S Kulacoglu ◽  
C Ozdem
Keyword(s):  
Case Report ◽  
Nasal Cavity ◽  
Nasal Septum ◽  
World Literature ◽  
Rare Case ◽  
Rare Tumour ◽  
Recurrent Epistaxis ◽  
The World ◽  
Sialadenoma Papilliferum

AbstractObjective:We report a rare case of sialadenoma papilliferum.Method:A case report of sialadenoma papilliferum is presented.Results:A 67-year-old woman presented with recurrent epistaxis. She was found to have an exophytic, well circumscribed mass on the nasal septum mucosa. The lesion was completely excised. A diagnosis of sialadenoma papilliferum was made based on the characteristic histological pattern. Follow up showed no evidence of recurrence. Subsequently, the patient remained well without complaint of epistaxis.Conclusion:To our knowledge, this is the first report in the world literature of sialadenoma papilliferum of the nasal cavity. This case indicates that this rare tumour can present with epistaxis, and can be resolved by means of total excision.

scholarly journals An Extranasopharyngeal Angiofibroma of Mandibular Ramus in a Preschool Child - An Extremely Rare Case Report

2021 ◽  
Vol 10 (28) ◽  
pp. 2128-2130
Author(s):  
Charan Teja Vemagiri ◽  
Chandrababu Pamidi ◽  
Srikanth Damera ◽  
Supraja Naga Atluri ◽  
Mounika Kallukuri
Keyword(s):  
Nasal Septum ◽  
Sphenoid Sinus ◽  
Rare Case ◽  
Ethmoid Sinus ◽  
Mandibular Ramus ◽  
Nasopharyngeal Angiofibroma ◽  
Male Adolescents ◽  
Sphenopalatine Foramen ◽  
Rare Case Report ◽  
Extranasopharyngeal Angiofibroma

Angiofibroma or juvenile nasopharyngeal angiofibroma (JNF) is a rare vascular benign tumour predominant in male adolescents and pre-adolescents. In spite of several origin sites reported, nasopharynx in the region of the sphenopalatine foramen and pterygopalatine fossa remains most common.1 Nevertheless, sporadic description of extra nasopharyngeal angiofibromas (ENAF) are also rarely evident.2 Literature documents maxillary sinus as the most favourable site for ENAF followed by the ethmoid sinus, nasal cavity, nasal septum, larynx, sphenoid sinus, cheek, conjunctiva, oropharynx, retromolar area and others.3 However, ENAF of mandibular ramus marks rarity and no case has been reported with respect to this anatomic location especially in preschool children yet. Hence, a rare ENAF in a 3-year-old child, principally confined to mandible, with neither sphenopalatine foramen nor nasopharynx involvement presenting with swelling is described.

Metronidazole ototoxicity - report of two cases

1999 ◽  
Vol 113 (4) ◽  
pp. 355-357 ◽  
Author(s):  
S. M. Iqbal ◽  
J. G. Murthy ◽  
P. K. Banerjee ◽  
K. A. Vishwanathan
Keyword(s):  
Hearing Loss ◽  
Case Report ◽  
Oral Administration ◽  
Sensorineural Hearing Loss ◽  
Steroid Therapy ◽  
World Literature ◽  
Sensorineural Hearing ◽  
Oral Steroid ◽  
The World ◽  
Oral Steroid Therapy

AbstractTwo cases of bilateral moderate to severe sensorineural hearing loss due to oral administration of metronidazole are reported. There has been only one case report of deafness following metronidazole therapy in the world literature. The hearing loss recovered gradually in a period of four to six weeks following withdrawal of drug and oral steroid therapy. The possible mechanism of ototoxicity is discussed. Awareness by the treating physician of ototoxicity due to any drug is stressed.

Dermatofibrosarcoma Protuberans Metastatic to the Lung. A Case Report

1992 ◽  
Vol 78 (1) ◽  
pp. 49-51 ◽  
Author(s):  
Prakash K. Patil ◽  
Snehal G. Patel ◽  
S. Krishnamurthy ◽  
Rajesh C. Mistry ◽  
Raman K. Deshpande ◽  
...  
Keyword(s):  
Case Report ◽  
World Literature ◽  
Dermatofibrosarcoma Protuberans ◽  
Primary Lesion ◽  
Wide Excision ◽  
Pathologic Features ◽  
The World ◽  
Long Term Follow Up

A case is presented of dermatofibrosarcoma protuberans of the gluteal region with metastasis to the lung appearing 7 years after wide excision of the primary lesion. The world literature is reviewed. The clinical and pathologic features of dermatofibrosarcoma are reviewed and treatment is discussed, with the aim of emphasizing the need for long-term follow-up examination of lymph nodes and for metastases following wide excision of these lesions.

Congenital cholesteatoma in identical twins

2012 ◽  
Vol 127 (1) ◽  
pp. 67-69 ◽  
Author(s):  
T Al Balushi ◽  
J Z Naik ◽  
M Al Khabori
Keyword(s):  
Case Report ◽  
World Literature ◽  
Rare Case ◽  
Identical Twins ◽  
Rare Entity ◽  
Ear Surgery ◽  
Congenital Cholesteatoma ◽  
The World ◽  
Local Trauma ◽  
Clinical Pictures

AbstractObjective:We present an extremely rare case of congenital cholesteatoma in identical twins.Method:Case report of congenital cholesteatoma in identical twins, and a literature review, are presented.Results:Both cases presented to the ENT out-patient clinic, but with different clinical pictures. Both were managed surgically.Conclusion:Congenital cholesteatoma presents as a whitish mass in the middle ear, with an intact tympanic membrane. It is a rare entity comprising between 3.7 and 24 per cent of total cholesteatoma cases. The key to its diagnosis is the absence of previous ear infection, ear surgery and local trauma. To our best knowledge, this paper represents the first report in the world literature of congenital cholesteatoma in identical twins.

Congenital cholesteatoma of occipital bone or intradiploic epidermoid cyst? One and the same disease

2008 ◽  
Vol 123 (6) ◽  
pp. 673-675 ◽  
Author(s):  
M P A Clark ◽  
P M Pretorius ◽  
D Beaumont ◽  
C A Milford
Keyword(s):  
Case Report ◽  
Middle Ear ◽  
Epidermoid Cyst ◽  
World Literature ◽  
Rare Case ◽  
Occipital Bone ◽  
Epidermoid Cysts ◽  
Congenital Cholesteatoma ◽  
Imaging Characteristics ◽  
The World

AbstractObjective:We report an extremely rare case of congenital cholesteatoma affecting the occipital bone.Methods:We present a case report, plus a review of the world literature on similar lesions.Results:This case report describes the presentation and treatment of a congenital cholesteatoma arising in an apparently unique location within the occipital bone, with no effect on middle-ear structure or function. The different imaging characteristics of this lesion are described and illustrated. The discussion centres on the differentiation of this lesion from intradiploic epidermoid cysts, more commonly described in the neurosurgical literature. The possible methods of pathogenesis are discussed, along with treatment suggestions.Conclusion:Congenital cholesteatomas and intradiploic epidermoid cysts are indistinguishable both histologically and radiologically, and would appear to be the same disease.

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