Indian Journal of Ophthalmology

: 1970  |  Volume : 18  |  Issue : 3  |  Page : 138--141

Scleroderma- a case report

Prabha Bhura, RK Mishra, BN Shrivastava 
 Department of Ophthalmology, Medical College, Jabalpur, India

Correspondence Address:
Prabha Bhura
Department of Ophthalmology, Medical College, Jabalpur

How to cite this article:
Bhura P, Mishra R K, Shrivastava B N. Scleroderma- a case report.Indian J Ophthalmol 1970;18:138-141

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Bhura P, Mishra R K, Shrivastava B N. Scleroderma- a case report. Indian J Ophthalmol [serial online] 1970 [cited 2020 Oct 29 ];18:138-141
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Ocular involvement of scleroderma is well known. Involvement of lid­skin and subcutaneous tissue is com­mon but intraocular involvement is not well classified. Cornea (Meunier and Toussaint [8] ), lens and uvea (Dol­fus) retina and optic nerve (Dol­fus [3] , Jostens, Curtis and Jansen [2] ) involvement have been reported.

We are reporting this case of a well marked diffuse scleroderma with associated skin changes in lids, mark­ed constriction of visual fields and pigmentary disturbances with colloid bodies spread over the retina.

 Case Report

Patient G. B., female, 35 years was admitted in the medical college hos­pital, Jabalpur on 12-2-67 with com­plaints of (1) swelling on legs, feet, forearms and hands - seven months, (2) anorexia - six months, (3) pain in hip and knee joints - one month, (4) headache - one month. The onset was insidious. She first obser­ved oedema on legs, feet and fore­arms. This was followed by develop­ment of articular pain and erythema. She later observed stiffness and pain in joints of hands and along with that hyperpigmentation of face.

Past illness:- Nothing- particular.

Personal history:- no: addiction to tobacco, sterilization operation four years ago, irritable by temperament.

On examination the patient had a set expressionless face [Figure 1] with skin of forehead, maxilla, lids, fore. arms, hands, dorsum of feet and legs thin, tense and shining. The skin gave an impression of being stretched over the underlying tissues. Pigmen­tation was noticed over the skin. The angle of mouth was stretched [Figure 2] giving a grinning appearance. There was a generalised stiffness of joints. The finger joints were particularly affected producing stiff claw like hands. [Figure 3]. The fingers felt wooden hard and even passive movements were difficult. The stiff tendons could be felt and the grip was poor. She had noticed blue colouration of hands and feet when dipped in cold water. This could be demonstrated by dipping her hands in ice cold water. Of late she had developed some diffi­culty in swallowing.

Ocular Findings:

The lid-skin was tense and shining and could not be lifted. The lids appeared to have lost their mobility and had become rigid. [Figure 1]. They could not be moved by a pull over the skin and an appearance of ptosis was present. The levators appeared to be weaker than normal.

The movements of eyeball were normal. The cornea, conjunctiva and pupils showed no abnormality. The lens was clear and in position.

Fundus examination revealed nor­mal discs, normal arteries and veins in calibre and ratio, but the: retinal ground showed colloid like lightly pigmented round deposits. Small pin point pigments were noticed on equa­torial region. Retinal reflex was slightly dull. The macular area showed pigmentation. [Figure 4]. In­traocular tension was normal and field of vision showed marked peripheral constriction with intact central vision. [Figure 5].


1. Urine and stool examination reports were negative.

2. Blood examination : E. S. R. - 20 mm at the end of first hour. Blood V . D . R . L . - negative, Blood urea - 28 mg %, Serum calcium - 16 mg %.

3. Plain X-ray of abdomen, chest and skull revealed no abnor­mality. On barium swallow it was found that the barium was held up at the lower end of oesophagus for 5 to 7 minutes. Slight irregularity was seen in the mucosal pattern. [Figure 6].

4. E.C.G. tracing was normal.

5. Conjunctival biopsy showed nonspecific changes.

6. Skin biopsy - "Changes con­sistent with scleroderma" was reported.


Scleroderma is an uncommon dis­ease of unknown aetiology. However, collagen disease is considered to be the most likely cause by many but others believe it to be neurotrophic in origin with a definite connection with the autonomic nervous system. It is characteristic and pathognomonic of scleroderma that the seemingly un­affected portion of skin too reveals a definite prolongation of nervous im­pulse.

The diffuse variety of this disease is called scleroderma. The term mor­phoca is applied to the localised type. This progressive disease may occur at any age affecting females about three times more commonly as males. In­ternal organs like heart, oesophagus and lungs are involved and ultimately death occurs from intercurrent infec­tion.

The disease probably starts as a vasospasm of the arterioles and oedema of the collagen bundles. A gradual occlusion; of the vessel follows and results in necrosis of the tissues. There is initial and subsequent atro­phy of skin and underlying tissues. At times even bones may be affected.

There seems to be no definite pat­tern of ocular involvement. The lid­skin shows induration, dispigmenta­tion and atrophy which may extend upto tarsal plate and levator palpebrae muscle causing ptosis. Occasionally there is paresis of other ocular mus­cles like superior and medial recti (Cords[1], 1928). Lesions of the sym­pathetic nerve may lead to Horner's syndrome.

The corneal sensation is reduced in some cases. Intraocular involve­ment has not been regularly described but iritis (Dolfus [3] ) iris atrophy, eye­litis and cataract formation arc re­ported. Changes in fundus have been described by many authors. Meunier and Toussaint [8] (1958), Dolfus [3] (1958). Josten [5] (1958) observed re­tinal haemorrhages, new vessels in. the disc and tortuous venules and a gene­ral picture resembling thrombosis. Sheathing of the blood vessels has been reported by Meunier and Tous­saint [8] . Curtis and Jansen [2] described an ipsilateral optic nerve neurocytoma with skin changes of sabre cut type of sclerodcrma in a patient aged four years who died of cerebral haemorr­hage. Lauber [7] (1927) described changes left by subsiding uvcitis with a complicated cataract and a eyeball atrophy on the side affected by hemi­atrophy. The ocular changes descri­bed in literature are a bit confusing as many of the cases do not clearly distinguish between sabre cut sclero­derma and Romberg's hemiatrophy (cases of Kahler [6] , Osborne [9] , Frances­chetti [4] and others). There is no doubt that these two conditions have a very close resemblance.

Segal, Jablonska and Mrzyglod [10] reported a case of sclerderma of the skin of the scalp, forehead and cheek in a man aged 43 years along with mild iritis, iris atrophy and deformed pupil.

In our case the most interesting finding was the pigmentary disturbance and colloid like bodies in the fundus associated with peripheral field con­striction. The pigmentation was pre­sent in both eyes in an identical fa­shion. The shape and size of pig­ments were quite different from retinitis pigmentosa. There was no history of night blindness and the re­tinal vessels were normal. No ex­planation could be found for the field loss and for the pigmentary changes. The deposits seemed quiet and stationary. No evidence of glaucoma or raised intracranial tension was found. There is no reference for pig­mentary changes in the fundus. Nar­rowed lumina of the capillaries may be responsible for pigmentary changes and peripheral field constriction.


A case of diffuse scleroderma with ocular changes is reported. The pa­tient had typical changes in the lids. There were multiple colloid like exu­dates and pigments all over the fundus. The visual fields were mar­kedly constricted.


1Cords, R. E.: Cordlikc facial atrophy and the eye (in Geman). Bericht. d. Deutsch. Ophth. Gesell., 47: 53, 1928.
2Curtis, A. C., and Janscn, T. G.: The prognosis of localized scleroderma. AMA Arch. Derniat., 78: 749, 1958.
3Dolfus, M.: Another case of sclero­dermia inn sabre-cut with multiple ocular lesions having evolved during more than 12 years. (In French) Bull. Soc. beig. Ophthal., 118: 377, 1958.
4Franccschetli, A., Jadassohn, W., Pail­lard, R., Hofer, R, and Golay, M.: Hemiatrophy facialis or sclerodcrma inn sabre-cut. (In French) Dermato­logica, 116: 331, 1958.
5Josten, K.: Scleroderma in sabre-cut and the Eye. (In German) Min. Monatsbl. f. Augenh., 133 : 567, 1958.
6Kahler. O.: A case of localised neu­ral facial atrophy (in German). Prager Mediz. Wchschr., 6: 53, 1881. (ref by Cords in 1).
7Lauber, H.: A case of progressive Hemiatrophy facialis with ocular participation. (In . German). Ztschr. Augenh., 57: 492, 1925.
8Meunier, A., and Toussaint, D.: Scleroderma in sabre-cut with lesions of the fundus of eye (in French). Bull. Soc. belg. Ophthal., 118: 369, 1958.
9Osborne, E. D.: Morphoea associa­ted with hemiatrophy of the face. Arch. Derm. & Syph., 6: 27, 1922.
10Segal, P., Jablonska, S. and Mrzy­glod, S.: Neurotrophic changes in the uvea in scleroderma in "coup de sabre". Klinika Oczna, 30: 381-388, 1960.