Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contacts Login 
  • Users Online: 9740
  • Home
  • Print this page
  • Email this page

   Table of Contents      
ARTICLE
Year : 1970  |  Volume : 18  |  Issue : 4  |  Page : 187-189

Albers - schonberg disease (osteopetrosis)


Assistant Professor of Neuro-Ophthalmology, Madurai Medical College, Madurai, India

Correspondence Address:
G Natchiar
Assistant Professor of Neuro-Ophthalmology, Madurai Medical College, Madurai
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:
Natchiar G. Albers - schonberg disease (osteopetrosis). Indian J Ophthalmol 1970;18:187-9

How to cite this URL:
Natchiar G. Albers - schonberg disease (osteopetrosis). Indian J Ophthalmol [serial online] 1970 [cited 2020 Aug 6];18:187-9. Available from: http://www.ijo.in/text.asp?1970/18/4/187/35641

This condition was first described by Albers Schonberg in 1904. Subse­quently, in 1926 Korshner gave the name of Osteopetrosis. It is a rare dis­ease characterised by increased density and thickness of both cortical and spongy bones, by spontaneous fractures and occasionally by changes in the blood resembling that of leukaemia. A distinct familial tendency is displayed and the disease is occasionally inheri­tant. It is due probably to an inborn error of calcium metabolism, but the exact metabolic defect is unknown. Long bones and bones of the skull are usually affected. The involved bones appear to be uniformly dense with par­tial or complete obliteration of the medullary space. The metaphyseal region of the long bones shows club like, thickening with remarkable in­crease in bone density, consequent re­duction in blood forming marrow which causes aplastic or leukaemic anaemia. Radiographically the affected parts of the bones have a dense homo­geneous appearance. These cases usu­ally attend Orthopaedic Department either for a pathological fracture or for a deformity in the skeletal system. Rrarely they come to ophthalmologists for prominence of the eye ball with defective vision. The ocular complica­tions of this disease are attributed solely to the results of pressure by the over­growth of the bone, on the eye or on the nerves of the eye and the lesion includes optic atrophy, exophthalmos, nystagmus, ptosis and papilloedema. Optic atrophy is commonly found in infants and children who suffer from a severe degree of this disease and it is not found in adults with osteopetrosis. Keith [2] , has reported a case of Osteo­petrosis with optic atrophy and he says that optic atrophy in that particular case was not due to bone pressure, but it was due to retinal atrophy and re­tinal degeneration which can also occur in osteopetrosis.


  Case Report Top


N.O., an 8 years old boy was referred to the Neuro Ophthalmic Department from the E.N.T. ward as a case of bilateral proptosis with defective vision.

History : The child was having headache, purulent ear discharge from the left ear since z years and for that he underwent mastoidectomy on the left side in 1966 and since then he was having a persistent sinus behind the left ear discharging pus. He developed difficulty in closing the left eye and deviation of the angle of the mouth after this operation. According to the parents, child was full term normal, had normal milestones. The child was not sent to school because of poor vision. They also noticed bilateral prominence of the eye balls with in­voluntary jerky movements.

Family History : The second child among the four siblings. None of the others have got similar complaints.

Examination : The child was ill looking and severely anaemic. The shape of the skull was peculiar. It appeared to be like a `tower skull' [Figure - 1]. He had multiple bony swel­lings over the skull, deformity of both arms and legs. Talipes varus deformity was also present in both feet. In addi­tion there was a bony prominence on the left side of the clavicle due to an old pathological fracture.

Ocular Examination : Child had bi­lateral proptosis and exophthalmometry reading was 28 mm. in both eyes. There was horizontal nystagmus which was present in all directions. Movements of the eye ball and eye lids were normal except for a facial nerve paralysis of lower motor neuron type left side [Figure - 2]. Pupils were slightly dilated and reaction was sluggish. Vision could not be recorded by Suellen's chart because he was too ill and because of poor co-operation ; approximately it could be about z/6o in both eyes. So also, the fields could not be charted.

Fundus examination revealed clear media, optic discs were pale with clear margin. No swelling of the disc was seen. Arteries were slightly narrowed. The picture was that of primary optic atrophy.

Other systems: Cardiovascular and respiratory systems were normal.

Abdominal Examination : Liver, spleen were not palpable.

With these findings, we thought the possibility of oxvcephaly and bilateral proptosis with optic atrophy were attri­buted to the deformity of the skull bone.

Radiographic examinations : X-ray skull showed increased density of the bone as we see in the picture. Hair brush bristle appearance was seen in the vault of the skull. There was also evidence of an old fractured clavicle on the left side. X-ray of long bones showed similar increased density and sclerosis of the bones. The diagnosis of Albers Schonberg disease was mainly made on radiological examination [Figure - 3],[Figure - 4]. Blood examination Haemoglobin was 5.4 gm% ; RBC 1.95 millions; WBC 12,000; Differential, P 4 8 L 4 8 E 4 . ESR was 142 mm. In 1 hour. There were no immature cells in peripheral blood smear. Urine exami­nation was normal.

The interesting point in this case was, the patient was referred to Neuro Ophthalmic Department from the E.N.T. Ward after mastoidectomy on the supposition that the proptosis and optic atrophy were due to some intra­cranial pathology following mastoid­ectomy. But the shape of the skull, abnormal bony swellings over the body gave us a clue regarding the actual diagnosis.


  Summary Top


A case of Osteopetrosis with bilateral exophthalmos and optic atrophy in a 8 years old boy is reported. The diagno­sis was mainly made on radiological examination[5].

 
  References Top

1.
Consul, B. N., Kulshrestha, O. P. and Sethi, P. K. - Osteopetrosis - Amer. J. Ophthal. 58: 686-690, 1964.  Back to cited text no. 1
    
2.
Keith, C. G. - Retinal Atrophy in Osteopetrosis. Arch. of Ophth. (Chi­cago), 79: 234-241, March 1968.  Back to cited text no. 2
    
3.
Walsh, F. B. - Clinical Neuro Ophthal­mology, Williams and Wilkins Com­pany, Baltimore, 1957.  Back to cited text no. 3
    
4.
Wills, P. and Sweetman, R. - Essentials injuries.  Back to cited text no. 4
    
5.
Watson, Jones R. - Fracture and joint of Orthopaedics.  Back to cited text no. 5
    


    Figures

  [Figure - 1], [Figure - 2], [Figure - 3], [Figure - 4]



 

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
Summary
References
Article Figures

 Article Access Statistics
    Viewed1913    
    Printed40    
    Emailed1    
    PDF Downloaded0    
    Comments [Add]    

Recommend this journal