Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contacts Login 
  • Users Online: 414
  • Home
  • Print this page
  • Email this page

   Table of Contents      
ARTICLE
Year : 1966  |  Volume : 14  |  Issue : 3  |  Page : 141-143

Osteoma of the orbit


Department of Ophthalmology, Medical College, Rohtak, India

Date of Web Publication16-Jan-2008

Correspondence Address:
M R Chaddah
Department of Ophthalmology, Medical College, Rohtak
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


Rights and PermissionsRights and Permissions

How to cite this article:
Chaddah M R, Ahluwalia B K. Osteoma of the orbit. Indian J Ophthalmol 1966;14:141-3

How to cite this URL:
Chaddah M R, Ahluwalia B K. Osteoma of the orbit. Indian J Ophthalmol [serial online] 1966 [cited 2020 Aug 7];14:141-3. Available from: http://www.ijo.in/text.asp?1966/14/3/141/38647

Osteoma of the orbit is relatively rare. Bullock and Reeves (1959) stud­ied 138 cases of unilateral exophthal­mos radiologically and did not find any case of osteoma. Ahluwalia (1964) in his survey of 25 cases of proptosis did not report any orbital osteoma. Moss (1962) while analysing Jone's and Reese's series of 230 cases of expand­ing lesions of orbit, found the inci­dence of osteoma to be one per cent. Ingall's (1953) review of 216 cases of tumours of the orbit revealed 2 cases of osteoma seen over a period of 12 years.

We have observed only 3 cases of osteoma of orbit over a period of 15 years.


  Case Report Top


Case l: R. S.: 30-year-old male farmer, presented on August 6, 64 with protrusion of the right eye since 5 months. About one month previously he had sustained a blunt injury to the medial part of the superior orbital margin. Swelling of the lids, pain, red­ness and watering subsided after 20 days of injury but proptosis and deteriorated vision persisted. Systemic examination revealed nothing abnor­mal. On local examination, the left eyeball was found to be normal. Right eyeball was proptosed forwards and slightly downwards and outwards by 6 mm. At the supero-medial angle of the orbit, palpation revealed an ill­-defined, painless, lobulated and a very hard fixed mass, about 1 cm x 1 cm extending backwards into orbit and it was firmly adherent to the bony orbit. Mobility of the globe was restricted up and in. Visual acuity was R 4/60.

L 6/12. Homatropine refraction re­vealed -- I D myopia R.E. but glasses did not benefit. Fundus examination revealed an oedematous and hyperemic disc with blurred margins and there was congestion of retinal veins. Blood counts and serology were non-contri­butory. Radiological investigation of the orbits demonstrated osteoma right side.

On Sept. 8, 64, a supero-medial orbi­totomy was performed under general anaesthesia. A sessile hard, white, lobulated and well-circumscribed osteo­ma 3.5 cm x 3 cm x 2.5 cm [Figure - 1] and weighing 22.83 gm. was removed after detaching the tendon of superior ob­lique which was restitched to the perio­steum.

The post-operative period was un­eventful with full eye movements and there was no diplopia. Diagnosis was confirmed by histopathological exami­nation. Oedema of the disc regressed and vision improved to R.E. 6/24 but glasses were of no benefit and it eventually led to partial optic atrophy.

Case II: T. D.: aged 23, a house­wife, presented on Jan. 30, 65 with prominence of left eyeball since 10 days. Preceding this, patient was aware of some heaviness of the left side of the head along with a hard and pain­less almond size mass in the left orbit since 21 years. There was no history of diplopia or nasal symptoms.

Pertinent ophthalmological findings were confined to the left eye. Palpebral fissure was narrow. There was an irre­ducible proptosis downwards and for­wards by 5 mm. Movements of the globe were restricted upwards. A lo­bulated, painless and ivory hard mass was palpable in the entire supero­medial part of the orbit; visual acuity was 6/36, Jii. Defective vision was due to three small corneal nebulae. Glasses did not effect improvement. Ophthal­moscopy was normal. General medical survey including urinalysis, blood ex­aminations revealed nothing abnormal. Roentgenological examination showed a large osteoma of the left orbit enter­ing into the frontal sinus [Figure - 2].

On Feb. 6, 1965, a supero-medial orbitotomy was carried out under ge­neral anaesthesia. Reflected tendon of superior oblique was stitched back to the periosteum after excision of the osteoma from its base. The osteoma was extending into the frontal sinus through an erosion of its floor. There was no intracranial extension. It was a hard, glistening white, nodular tu­mour partly covered by mucous mem­brane, measuring 2.75 cm x 2.25 cm x 1.5 cm and weighing 8.62 gm. Micros­copic examination confirmed the diag­nosis of ostcoma. Convalescence was uneventful.


  Discussion Top


In our experience, osteoma of the orbit is a rare cause of unilateral prop­tosis and this observation finds support from the work of many authors (Bul­lock and Reeves, 1959; Ahluwalia, 1964: Moss 1962: and Ingalls, 1953).

Patient of orbital osteoma may pre­sent with ocular, cerebral or nasal symptoms depending upon site of origin of the tumour, with many re­maining a symptomatic.

One of the cases showed papilloe­dema which was explained by raised intraorbital pressure and compression of the optic nerve. This, however, re­gressed after surgery leaving behind partial optic atrophy. The diagnosis of osteoma is confirmed by radiologi­cal examination and the only treatment in cases with symptoms is timely sur­gical excision. Commonly the tumour originates from the paranasal sinuses and invades the orbit mostly at the supero-medial angle. This was true of our cases where one sessile growth was arising from anterior ethmoidal cells and the other was from frontal sinus. The latter had eroded the outer part of the floor of the frontal sinus. Before undertaking surgery, it is imperative to carefully study the origin and size of the tumour as well as to exclude or determine the extent of the intracra­nial extension. None of our cases had spread to the cranial cavity. The only difficulty encountered during surgical excision is the injury and subsequent dysfunction of superior oblique muscle. This could be prevented by detaching the tendon of superior oblique from the pulley and stitching it back to the periosteum after removal of the growth.


  Summary Top


Incidence of orbital osteoma is dis­cussed and two such cases, one each arising from ethmoidal sinus and frontal sinus, are presented. Both tu­mours were removed successfully via an anterior orbitotomy without post­operative diplopia.


  Acknowledgement Top


We wish to extend our gratefulness to Dr. G. C. Mehrotra, Professor of Pathology. Medical College. Rohtak, for his help in Histopathological study.[4]

 
  References Top

1.
Ahluwalia, B, K. (1964): Thesis for M.S. examination, Punjab University.  Back to cited text no. 1
    
2.
Bullock. L. J.; and Reeves, R.J.; (1959). Amer. J. Roentgenol. 82: 290-299.  Back to cited text no. 2
    
3.
Ingalls, R. G. (1953): Tumours of the orbit and allied Pseudotumours. p. 273-­280. Charles C. Thomas Publishers Spring Field U.S.A.  Back to cited text no. 3
    
4.
Moss, H. MacMillan (1962): Amer. J. Ophth. 54: 761-770.  Back to cited text no. 4
    


    Figures

  [Figure - 1], [Figure - 2]



 

Top
 
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
Case Report
Discussion
Summary
Acknowledgement
References
Article Figures

 Article Access Statistics
    Viewed1495    
    Printed31    
    Emailed0    
    PDF Downloaded0    
    Comments [Add]    

Recommend this journal