Br J Ophthalmol: first published as 10.1136/bjo.68.8.590 on 1 August 1984. Downloaded from British Journal ofOphthalmology, 1984, 68, 590-594 Disc oedema in association with Hunter's syndrome: ocular histopathological findings MARILYN BECK' AND GILLIAN COLE2 From the 'Department of Ophthalmology, University Hospital of Wales, Heath, Cardiff CF4 4XW, and the 2Department of Pathology, Welsh National School of Medicine, Heath Park, Cardiff CF4 4XN SUMMARY The histopathology of the posterior half of one eye and the optic nerves of a man with Hunter's syndrome, who was known to have disc oedema without raised intracranial pressure for 11 years of his life, is reported. The possible pathogenesis of the disc oedema is discussed; an important contributory factor was the deposition of abnormal mucopolysaccharides within the sclera. This caused gross thickening of the sclera with compression of the optic nerve at the intrascleral level. Hunter's syndrome was first described in 1917' and is episodes of heart failure when he was aged 25 years. one of the mucopolysaccharidoses. McKusick2 sub- A cousin also had Hunter's syndrome and died of divided this group of inherited disorders ofconnective respiratory failure following dental surgery. tissue into seven types. Hunter's syndrome is classified He was first seen by an ophthalmologist in 1971. as type II MPS and may be further subdivided into His visual acuities with a hypermetropic correction type IIA (severe) and type IIB (mild) depending on were 6/6 right and 6/6 left eyes. Fundal examination the degree of intellectual impairment. This disease is was recorded as showing normal peripheral fundi but usually inherited as an X-linked recessive trait. 'bilateral disc blurring.' http://bjo.bmj.com/ Clinically this syndrome is characterised by short In 1972 he was found to have gross bilateral disc stature, a gargoyle facies, stiff joints, hepato- swelling, normal retinal vessels, and normal splenomegaly, and cardiac abnormalities. Variable peripheral fundi. Visual fields recorded on the degrees of mental subnormality occur, and pro- Goldmann perimeter were full peripherally, but the gressive deafness is a consistent feature. In the mild blind spots were enlarged. Fluorography confirmed form survival has been reported to the sixth decade, that this was true disc oedema. He was then seen at whereas in the severe form death usually occurs before six-monthly intervals until March 1982. The corrected on September 26, 2021 by guest. Protected copyright. 15 years of age. Ocular abnormalities described in acuities 6/6 right and left were retained despite the this condition include exophthalmos, hypertelorism, fact that his disc appearances remained unchanged. papilloedema, and a pigmentary retinopathy, but the The visual fields remained full peripherally, but there cornea is usually macroscopically clear. were increasing scotomata centrally due to the This patient with Hunter's syndrome has been pre- development of a pigmentary retinopathy which was viously described,- as he was known to have disc first noted in 1980. The patient died of respiratory oedema for 11 years but yet retained good visual complications following hip surgery in September acuity. 1982. Case report POST-MORTEM EXAMINATION The patient had the characteristic external appear- This man, born 9 December 1947, was diagnosed as ance of Hunter's syndrome. There was generalised having Hunter's syndrome when he was aged 4 years thickening of bone and collagenous structures, with because of his small stature, facial appearance, deaf- particular involvement of the hip joints, mitral valve, ness, hepatosplenomegaly, and joint restriction. He larynx, and trachea with marked tracheal stenosis. was of normal intelligence, but he suffered from Brain and spinal cord. The brain was large and recurrent chest infections as a child and had his first weighed 1700 g. The dura covering brain and spinal Correspondence to Mairilyn Beck, FRCS. cord was markedly thickened. Coronal sections did 590 Br J Ophthalmol: first published as 10.1136/bjo.68.8.590 on 1 August 1984. Downloaded from Disc oedema in association with Hunter's syndrome: ocular histopathologicalfindings 591 Fig. Sections ofposterior halfof eye. The sc/era is grossly thickened, and the intrascleralportion ofthe optic nerve is compressed. Bulging ofthe optic nerve is evident. (HE, x4- 7). not show any macroscopic abnormality. The ven- stained with haematoxylin and eosin (HE), Kluver tricles were of normal size. Microscopic examination Barrer (KLB) stain for myelin, phosphotungstic acid showed the only obvious pathological change to be a haematoxylin (PTAH) for glial fibres and collagen, mild deposition of mucopolysaccharides (MPS) with- periodic acid schiff reagent (PAS) and colloidal iron in vessel walls, with a consequent perivascular for neutral and acid mucopolysaccharides. rarefaction of tissue. No MPS accumulation within neurones or glial cells ofthe brain or cord was evident. MICROSCOPIC EXAMINATION Eye and optic nerves. The posterior half of the right Sclera. The sclera was grossly thickened. Measure- http://bjo.bmj.com/ eye and both optic nerves were available for exam- ment of the thickness of the sclera at the posterior ination. Sections of the eye and optic nerves were pole revealed it to be 2-9 mm, which was nearly three embedded in paraffin and cut at 5 .tm. Sections were times thicker than the average 1 mm thickness of a similar site in three control eyes (Fig. 1). The sclera was thickened by irregular bands of densely col- lagenous tissue. Scattered throughout the sclera were clumps of granular deposits, which were present in macrophages, and also apparently lying free in the on September 26, 2021 by guest. Protected copyright. tissue. The granular material proved to be MPS, staining positively with PAS and colloidal iron. Choroid. The posterior choroid was the only uveal tissue available for examination and was essentially normal. There were sparsely scattered deposits of MPS confined to vessel walls. Bruch's membrane was intact. Retina. Numerous levels of the posterior retina were examined. The retinal pigment layer had been completely destroyed, and there was marked loss of rods and cones. In those areas where rods and cones could still be detected the normal architecture was lost. Occasional eosinophilic amorphous structures Fig. 2 Retina showing loss of rods and cones, and were evident, and this was interpreted as a degenera- formation ofamorphous structures (arrow). The outer and tive change (Fig. 2). The appearance of the rod and inner nuclear layers and the ganglion cells are reduced in cone layer was not considered to be artefactual or due number. (HE, X250). to poor fixation, since the other layers of the retina Br J Ophthalmol: first published as 10.1136/bjo.68.8.590 on 1 August 1984. Downloaded from 5'92 Marilyn Beck and Gillian Cole were well preserved. The outer and inner nuclear thickened at the lamina cribrosa and throughout its layers were considerably reduced, being about half extent. Finely scattered MPS granules which were the normal cell thickness seen in controls. The PAS and colloidal iron positive were present in the ganglion cells were likewise reduced in number septa. The vessels within the optic nerve contained (Fig. 2). small amounts of positively staining material, indica- There was moderate gliosis within the ganglion cell tive of MPS within their walls, but the bulk of MPS layer. No deposits of acid mucopolysaccharide were appeared to be in the region of the collagenous septa evident within the retinal layers or ganglion cells. within the nerve. The presence of scanty MPS There was, however, a mild deposition of MPS within granules within macrophages in the region of the and around the vessel walls. Retinitis pigmentosa was septa was best demonstrated on thin toluidine blue present with accumulation of pigment within macro- sections. Sections of the optic nerve in its peripheral phages and lying free in the tissue. The pigment extent from the optic chiasm revealed essentially the tended to accumulate around blood vessels. same features of thickened septa and gliosis. The Optic nerves. At the intrascleral level the optic gliosis, however, was mostly confined to the external nerve was considerably compressed by the thickened fibres beneath the thickened meningeal coverings, sclera (Fig. 1). There was marked gliosis of the nerve and was less extensive than that seen in the optic at the papilla (Fig. 3) and at the intrascleral level. nerve head and intrascleral portion. Microscopic evidence of disc oedema was most con- vincingly demonstrated by changes in the optic nerve ELECTRON MICROSCOPY head, which bulged forwards and laterally with some Formalin fixed tissue was rehydrated from paraffin displacement of the retina away from the disc margins blocks, and refixed in phosphate buffered glutaralde- (Fig. 1). The collagenous septa of the nerve were hyde. After post-osmication and post-fixing in 1.5% A http://bjo.bmj.com/ on September 26, 2021 by guest. Protected copyright. Fig. 3 Optic nierve papilla with marked glialfibreformnatioti. (PTA H, x250). Br J Ophthalmol: first published as 10.1136/bjo.68.8.590 on 1 August 1984. Downloaded from Disc oedema in association with Hluter's synidrome: ocular histopathologicalfindings 593 '4!M. ' ;' <F te ; '$ , u I Ar, '4 v-. http://bjo.bmj.com/ Fig. 4 Scleralfibroblast withi initracloplasmini membratne bolund vacuoles conitaininlg lamellar atnd electron- detise iniclusion.s. N=nucleus. L =latnellar inclusions. (=collagen. (X 15000). aqueous uranyl acetate, pieces of choroid, sclera, and oedema was not a feature in these reports, and the optic nerve were dehydrated and embedded in Epon. optic nerves were found to be normal. We have Ultrathin sections were stained in lead citrate and described the histopathology and ultrastructure of on September 26, 2021 by guest. Protected copyright. viewed under a Philips 300 electron microscope. the posterior half of the eye of a patient with Hunter's In the choroid and sclera abnormal mucopolysac- syndrome who had unexplained disc oedema.