Juvenile angiofibroma(sbo-2) 
Juvenile angiofibroma is an uncommon,benign &extremely vascular tumour that arises in the tissues 
within the sphenopalatine foramen.It develops almost exclusively in adolencent males,though there 
are reports of this tumour being found in children,elderly,young,even pregnant women.Juvenile 
angiofibroma are locally invasive. 
Pathogenesis 
Juvenile angiofibroma present as well-defined,lobulated tumour that are covered by nasopharyngeal 
mucosa.The tumour consists of proliferating,irregular vascular channels wthin a fibrous 
stroma.Tumour blood vessels typically lack smooth muscle &elastin fibres.The stromal component is 
made up of plump of cells that can be spindle or stellate in shape& give rise to varing amount of 
collagen.It makes the tumour firm to hard while others may be soft. 
Androgen receptors are present in at least 75% of the tumour.Progesterone receptors may present 
in small proportion of tumour. 
Juvenile angiofibroma have also been reported to develop 25 times more frequently in patient with 
familial adenomatous polyposis. 
Presentation 
Recurrent severe epistaxes acompaned by progressive nasal obstruction are the classical symptoms 
of juvenile angiofibroma.These tumours don’t grow fast &so many months even years may pass 
before it appear to the patients.In most cases,there is a delay of at least 6 to 7 months between the 
onset of symptoms & presentation.By that time, it is usual for the youth to have other signs& 
symptoms of tumour growth &extension. Swelling of check ,trismus, hearing loss & nasal 
intonationof voice. 
Anterior rhinoscopy is likely to confirm the presence of aboundant mucopurulent secretion in the 
nasal cavity that obscure the vision. 
Soft palate is often displaced inferiorly by the bulk of tumour which can be seen pink or reddish 
mass. 
Assessment 
x-ray of skull lateral view shows anterior bowing of the posterior wall of the maxillary sinus. 
CT imaging allows for delineation of tumour extent:Classic CT finding include erosion of the medial 
pterygoid plate & indentation of the posterior wall of the maxillary sinus(Halman-muller sign). 
MRI is helpful in defining tumour extension in pterygopalatine fossa ,infratemporal fossa, or 
intracranial extension. 
Angiography is performed within 48hrs of surgery to define the tumour blood supply & to 
embolisation of the feeding.
Several staging systems have been proposed but that of FISCH is the most robust & practical. 
Type Details 
1 Tumour limited to the nasopharyngeal 
cavity;bone destruction negligible or limited to 
the sphenopalatine foramen. 
2 Tumour invading the pterygopalatine fossa or 
the maxillary ,ethmoid or sphenoid sinus with 
bone destruction. 
3 Tumour invading the infratemporal or orbital 
region: a) without intracranial involvement. 
b) with intracranial extradural involvement. 
4 Intracranial intradural tumour.a)without 
infiltration of the cavernus sinus ,pituitary fossa 
or optic chiasma.b) with infiltration of the 
cavernous sinus ,pituitary fossa or optic chiasma. 
Treatment: 
Recognized by ancient times by Hippocrates & called Hard nasal polyp. 
Preoperative embolization;The role of preoperative embolization is controversial.More extensive 
tumour acquire a blood supply from others vessels.The maxillary or external carotid artery can be 
controlled by ligation relatively easy.Recurrence rate is increased by preoperative 
embolizaton,Perhaps shrinkage of the tumour makes it more difficult to define its entirety at the 
bottom of a deep& bloody operative field. 
Peoperative chemotherapy 
Ostrogens shrinkage in some but effect is variable &secondary feminizaion effect by an adolescent 
boy. 
Androgen receptor blocker Flutamide,tumour shrinkage of upto 44% used in the management of 
prostate cancer. 
Surgical resections 
Most small tumour can resected through a transpalatal approach,Lateral rhinotomy approach or 
Mid-facial degloving approach. 
Now a days stage Fisch 1,2&some type 3 tumours are suitable for endoscopic approach using one or 
two surgeon techniques. Advantage of endonasal endoscopic techniques are reduced intraoperative 
bleeding,fewer postoperative complications,& reduced length of hospital stay.
Endoscopic endonasal techniques 
Under G/A the nose is prepared with vasoconstrictor solution,the anterior end of middle turbinate is 
resected>anterior ethmoidectomy+removal of the medial wall of the maxillary sinus to get access to 
the posterior wall of the antrum.>Dissection into the sphenoidal rostrum. 
Second surgeon through contralateral nostril aids resection of large tumour>apply traction to the 
tumour. 
Open approaches 
Most surgeons now have adopted the technique of mid-facial degloving for the resection of 
angiofbromas.Using the exposure afforded by this approach ,anterior ,medial,lateral&posterior walls 
of the maxillary antrum can be removed preserving a rim of bone around the nasal aperture & infra-obital 
nerve.This produces a very large cavity that is confluent with nasal cavity & post-nasal space. 
Radiotherapy 
External beam radiation in several fractions to achieve a total dose of 30-55Gy. 
Regression of angiofibrioma is very slow,often taking 2 to3 yrs before radiological stabilization. 
Complications 
Recurrence of the tumour 25% regardless of method of treatment.Further recurrence may develop 
in up to 40% of the patients. 
Recurrence is more with advanced disease.preoperative embolizaton& young patients. 
Surgical standpoint,most recurrence develop invasion of basisphenoid,drilling out of the 
basisphenoid ensure that no recurrence. 
Infra-orbital nerve sensory & vestibular stenosis deficit are recognised in mid-facial degloving 
approach.Prolonged nasal crusting is also common>regular nasal douching with saline &use of 25% 
glucose in glycerine can alleviate this.

Juvenile angiofibroma (sbo 2)

  • 1.
    Juvenile angiofibroma(sbo-2) Juvenileangiofibroma is an uncommon,benign &extremely vascular tumour that arises in the tissues within the sphenopalatine foramen.It develops almost exclusively in adolencent males,though there are reports of this tumour being found in children,elderly,young,even pregnant women.Juvenile angiofibroma are locally invasive. Pathogenesis Juvenile angiofibroma present as well-defined,lobulated tumour that are covered by nasopharyngeal mucosa.The tumour consists of proliferating,irregular vascular channels wthin a fibrous stroma.Tumour blood vessels typically lack smooth muscle &elastin fibres.The stromal component is made up of plump of cells that can be spindle or stellate in shape& give rise to varing amount of collagen.It makes the tumour firm to hard while others may be soft. Androgen receptors are present in at least 75% of the tumour.Progesterone receptors may present in small proportion of tumour. Juvenile angiofibroma have also been reported to develop 25 times more frequently in patient with familial adenomatous polyposis. Presentation Recurrent severe epistaxes acompaned by progressive nasal obstruction are the classical symptoms of juvenile angiofibroma.These tumours don’t grow fast &so many months even years may pass before it appear to the patients.In most cases,there is a delay of at least 6 to 7 months between the onset of symptoms & presentation.By that time, it is usual for the youth to have other signs& symptoms of tumour growth &extension. Swelling of check ,trismus, hearing loss & nasal intonationof voice. Anterior rhinoscopy is likely to confirm the presence of aboundant mucopurulent secretion in the nasal cavity that obscure the vision. Soft palate is often displaced inferiorly by the bulk of tumour which can be seen pink or reddish mass. Assessment x-ray of skull lateral view shows anterior bowing of the posterior wall of the maxillary sinus. CT imaging allows for delineation of tumour extent:Classic CT finding include erosion of the medial pterygoid plate & indentation of the posterior wall of the maxillary sinus(Halman-muller sign). MRI is helpful in defining tumour extension in pterygopalatine fossa ,infratemporal fossa, or intracranial extension. Angiography is performed within 48hrs of surgery to define the tumour blood supply & to embolisation of the feeding.
  • 2.
    Several staging systemshave been proposed but that of FISCH is the most robust & practical. Type Details 1 Tumour limited to the nasopharyngeal cavity;bone destruction negligible or limited to the sphenopalatine foramen. 2 Tumour invading the pterygopalatine fossa or the maxillary ,ethmoid or sphenoid sinus with bone destruction. 3 Tumour invading the infratemporal or orbital region: a) without intracranial involvement. b) with intracranial extradural involvement. 4 Intracranial intradural tumour.a)without infiltration of the cavernus sinus ,pituitary fossa or optic chiasma.b) with infiltration of the cavernous sinus ,pituitary fossa or optic chiasma. Treatment: Recognized by ancient times by Hippocrates & called Hard nasal polyp. Preoperative embolization;The role of preoperative embolization is controversial.More extensive tumour acquire a blood supply from others vessels.The maxillary or external carotid artery can be controlled by ligation relatively easy.Recurrence rate is increased by preoperative embolizaton,Perhaps shrinkage of the tumour makes it more difficult to define its entirety at the bottom of a deep& bloody operative field. Peoperative chemotherapy Ostrogens shrinkage in some but effect is variable &secondary feminizaion effect by an adolescent boy. Androgen receptor blocker Flutamide,tumour shrinkage of upto 44% used in the management of prostate cancer. Surgical resections Most small tumour can resected through a transpalatal approach,Lateral rhinotomy approach or Mid-facial degloving approach. Now a days stage Fisch 1,2&some type 3 tumours are suitable for endoscopic approach using one or two surgeon techniques. Advantage of endonasal endoscopic techniques are reduced intraoperative bleeding,fewer postoperative complications,& reduced length of hospital stay.
  • 3.
    Endoscopic endonasal techniques Under G/A the nose is prepared with vasoconstrictor solution,the anterior end of middle turbinate is resected>anterior ethmoidectomy+removal of the medial wall of the maxillary sinus to get access to the posterior wall of the antrum.>Dissection into the sphenoidal rostrum. Second surgeon through contralateral nostril aids resection of large tumour>apply traction to the tumour. Open approaches Most surgeons now have adopted the technique of mid-facial degloving for the resection of angiofbromas.Using the exposure afforded by this approach ,anterior ,medial,lateral&posterior walls of the maxillary antrum can be removed preserving a rim of bone around the nasal aperture & infra-obital nerve.This produces a very large cavity that is confluent with nasal cavity & post-nasal space. Radiotherapy External beam radiation in several fractions to achieve a total dose of 30-55Gy. Regression of angiofibrioma is very slow,often taking 2 to3 yrs before radiological stabilization. Complications Recurrence of the tumour 25% regardless of method of treatment.Further recurrence may develop in up to 40% of the patients. Recurrence is more with advanced disease.preoperative embolizaton& young patients. Surgical standpoint,most recurrence develop invasion of basisphenoid,drilling out of the basisphenoid ensure that no recurrence. Infra-orbital nerve sensory & vestibular stenosis deficit are recognised in mid-facial degloving approach.Prolonged nasal crusting is also common>regular nasal douching with saline &use of 25% glucose in glycerine can alleviate this.