Bilateral, independent juvenile nasopharyngeal angiofibroma: case report

2015 ◽  
Vol 129 (10) ◽  
pp. 1032-1035 ◽  
Author(s):  
M-L Mørkenborg ◽  
M Frendø ◽  
T Stavngaard ◽  
C Von Buchwald

AbstractBackground:Juvenile nasopharyngeal angiofibroma is a benign, vascular tumour that primarily occurs in adolescent males. Despite its benign nature, aggressive growth patterns can cause potential life-threatening complications. Juvenile nasopharyngeal angiofibroma is normally unilateral, originating from the sphenopalatine artery, but bilateral symptoms can occur if a large tumour extends to the contralateral side of the nasopharynx. This paper presents the first reported case of true bilateral extensive juvenile nasopharyngeal angiofibroma involving clinically challenging pre-surgical planning and surgical strategy.Case report:A 21-year-old male presented with increasing bilateral nasal obstruction and discharge. Examination revealed tumours bilaterally and imaging demonstrated non-contiguous tumours. Pre-operative angiography showed strictly ipsilateral vascular supplies requiring bilateral embolisation. Radical removal performed as one-step, computer-assisted functional endoscopic sinus surgery was performed. The follow-up period was uncomplicated.Conclusion:This case illustrates the importance of suspecting bilateral juvenile nasopharyngeal angiofibroma in patients presenting with bilateral symptoms. Our management, including successful pre-operative planning, enabled one-step total removal of both tumours and rapid patient recovery.

2021 ◽  
Vol 6 (1) ◽  
pp. 45-52
Author(s):  
Marlinda Adham ◽  
Kartika Hajarani ◽  
Lisnawati Rachmadi ◽  
Indrati Suroyo

1979 ◽  
Vol 87 (1) ◽  
pp. 42-46 ◽  
Author(s):  
Paul J. Donald

Malignant degeneration in a juvenile nasopharyngeal angiofibroma has been reported in the literature in only four patients. All of these persons had been previously treated for cure with gamma irradiation. The case report of a 47-year-old man with a 31-year history of nasal obstruction is presented. A recurrence excised 18 months after initial removal of an angiofibroma revealed the surprising diagnosis of fibrosarcoma.


BioMedicine ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 41-44
Author(s):  
Mojtaba Mohammadi Ardehali ◽  
Shirin Irani ◽  
Mohammadreza Firouzifar

2019 ◽  
Vol 12 (4) ◽  
pp. e229376 ◽  
Author(s):  
Bruno Galletti ◽  
Francesco Gazia ◽  
Cosimo Galletti ◽  
Francesco Galletti

We present a case of a 16-year-old girl with interruption of papyracea lamina and herniation of the periorbital fat covered by a bone shell. The patient presents with a history of diplopia and visual disturbances ever since she can remember. Thanks to radiological imaging and biopsy, we have done differential diagnosis with periorbital lipoma, intraosseous lipoma and intramuscular lipoma of medial rectus. Diagnostic for images is necessary for a correct operative planning. Endoscopic sinus surgery with computer-assisted navigation is the safest and most effective method to remove the lesion that was closely related to the medial rectum muscle and to the anterior ethmoidal artery. The patient after surgery and in 1 year of follow-up reports the disappearance of symptoms.


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