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Optic Neuropathy and Macular Chorioretinal Folds Caused by Orbital Cherubism
Arch Ophthalmol. 2003;121:570-573.
Cherubism is a rare fibro-osseous disease of the maxilla and mandible usually seen in childhood. Orbital manifestations are proptosis, lower eyelid retraction, and upward displacement of the globes. Previous cases of orbital cherubism with unspecified visual change have been documented.1-2 We present a case of orbital cherubism with visual loss directly attributable to optic neuropathy and macular striae/scarring that resulted from the effect of the mass or tumor pushing on the eye of the orbital lesion.
Clinicopathogic Report
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A 31-year-old hispanic woman with a known history of cherubism was referred by the Oral Maxillofacial Surgery Service to the Department of Ophthalmology for evaluation of decreased vision in her left eye. She had undergone mandibular osteoplasty 3 months earlier for treatment of facial deformity secondary to cherubism.
When we saw her (Figure 1, A), the patient complained of mildly decreased vision in her left eye, intermittent diplopia on far lateral gaze, and tearing. She also admitted to intermittent photopsias and floaters of 4 months' duration. On examination, her corrected visual acuity was 20/20 OD and 20/30 OS with a correction of –1.00 + 1.50 x 90 OD and –1.00 + 1.75 x 120 OS, respectively. She had a relative afferent pupillary defect in her left eye and scored 15/15 OU on Ishihara color plate testing. Hertel exophthalmometry readings were symmetrical at 18 mm OU at a base of 87 mm. Extraocular motility was diminished on upgaze and lateral gaze in both eyes. Examination of the eyelids revealed a margin-reflex distance of 1.5 mm OD and 2 mm OS with good levator function. She displayed 3 mm of inferior scleral show with 1 to 2 mm of lagophthalmos in both eyes. Results of slitlamp examination revealed inferior punctate keratopathy with mild conjunctival hyperemia in both eyes. The remaining anterior segment examination findings were within normal limits. Funduscopic examination results were unremarkable in the right eye and showed temporal disc pallor and macular chorioretinal folds and scarring in the left eye (Figure 2, A). Cranial nerves II through VII were tested and intact. Humphrey visual fields were performed and revealed a generalized depression in the left eye with a relative paracentral scotoma (mean deviation, -14.34 dB, P<0.5%). The visual field in her right eye was within normal limits (mean deviation, -6.01 dB, P<0.1%).
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Figure 1. A, Preoperative photograph. B, Photograph taken 4 months postoperatively. Note the improvement in scleral show and decreased upward and inward displacement of the globes.
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Figure 2. A, Preoperative fundus photograph. B, Postoperative photograph. Note the improvement in macular striae/scarring. Also, there is temporal pallor of the optic nerve.
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Computed tomographic scans of the sinuses/orbits were performed and showed an expansile, at least partially osseous, mass invading the maxillary sinuses and the orbits bilaterally, with resultant remodeling of the orbits (Figure 3, A and B). The orbital extension of the mass was greater on the left than the right, with resultant medial and superior shift of orbital contents. The optic nerves were displaced medially and were draped across the mass. The mass abutted on the globe posteriorly. These findings were unchanged from the scans performed 3 months earlier by the Oral Maxillofacial Surgery Service.
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Figure 3. A, Preoperative coronal computed tomographic (CT) scan. B, Preoperative axial CT scan. C, Coronal CT scan 2 days postoperatively. Note the decreased height of the maxillary fibro-osseous columns.
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It was decided to perform staged orbital decompression surgery, left eye followed by the right eye, with curettage of the lesion. After obtaining informed consent from the patient, preoperative embolization of the internal maxillary arteries and the transfacial branch from the superficial temporal artery was performed to optimize intraoperative hemostasis.
A transconjunctival approach was used to reach the inferior orbital rim periosteum. The periosteum of the floor was reflected off the bone using Freer elevators, and a 2 x 3-cm bony mass was visualized. Using a reciprocating saw blade and osteotomes, an osteotomy was performed and the bony mass was debulked and sent for histopathological diagnosis. The floor was then smoothed down using a reciprocating rasp. The wound was then irrigated with isotonic sodium chloride and suctioned dry. Hemostasis was achieved with the help of bone wax. The conjunctiva was closed with multiple interrupted 6-0, fast-absorbing plain gut sutures. Intermittent pupillary checks performed during surgery encountered no abnormalities.
On histopathology, sections showed lamellar and woven bone, osteoblast proliferation, and cellular zones composed of spindled, fibrous stroma with numerous, scattered multinucleated giant cells (Figure 4). The findings were consistent with the clinical diagnosis of cherubism.
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Figure 4. Fibrous stroma with scattered multinucleated giant cell adjacent to bone seen on histopathological examination (hematoxylin-eosin, original magnification: A, x40; B, x10).
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Postoperative CT scans were performed and revealed debulked orbital masses with decreased proptosis (Figure 3, C). On ophthalmic examination 4 months after surgery, her visual acuity had remained unchanged. Hertel exophthalmometry readings were unchanged, but her dystopia had resolved. Although the macular folds had improved, some residual scarring remained (Figure 2, B). Her facial appearance improved with her globes and eyelids returning to a normal anatomic position (Figure 1, right).
Comment
Cherubism is a fibro-osseous disease of childhood characterized by bony expansile lesions of the maxilla and mandible. Jones3 coined the term "cherubism" after the angelic features seen in Baroque art of the Renaissance period. These figures had round, full-cheeked faces whose eyes "turned up to the heavens."4 The mode of transmission is autosomal dominant with 80% to 100% penetrance and variable expressivity.5 The gene was localized recently to chromosome 4p16.3 in a study of 2 affected families.6 Patients affected with this disease are generally without these distinguishing characteristics at birth. Onset of the disease process occurs between 2 and 4 years of age with painless expansion of the mandible and occasionally the maxilla. This causes facial deformities and abnormalities of dentition.3 The disease generally progresses until puberty and may regress in adulthood.4 Radiologically, the radiolucent bony lesions are cystic and multiloculated in nature and are bilateral.4 These findings in conjunction with the clinical presentation are usually enough to make a diagnosis. Unless surgical intervention is needed for genetic or reconstructive purposes, a confirmatory biopsy is not obligatory. If a biopsy is performed, the histopathological differential diagnosis of lamellar bone formation with fibrous stroma and giant cell formation includes fibrous dysplasia, aneurysmal bone cyst, central giant cell granuloma of bone, and brown tumor of hyperparathyroidism.4 However, on the basis of clinical presentation and laboratory data, alternative diagnoses can be ruled out. Indications for treatment include functional problems, such as dental abnormalities and visual compromise, and the need for cosmesis. Treatment of choice is surgical curettage and contouring.7 Radiation therapy is not recommended because of risks of osteonecrosis and sarcoma transformation.5
We present a case of cherubism with documented visual loss secondary to optic neuropathy and macular chorioretinal folds/scarring directly attributable to compression from the fibro-osseous growth within the orbit. To our knowledge, only 3 other cases of cherubism have been described in the ophthalmic literature.2, 4 None of these cases presented with a relative afferent pupillary defect indicative of optic neuropathy. Although Hawes2 presented a patient with visual loss secondary to macular scarring, he did not attribute this to globe compression from the fibro-osseous mass. Since most reports on this disease are presented in the oral maxillofacial and otorhinolaryngology literature (MEDLINE search of the past decade reveals 2 articles in ophthalmology journals and 37 in the two aforementioned fields), the focus is not on ophthalmic manifestations of disease and etiology of visual loss. It is therefore quite possible that visual loss from optic neuropathy and/or maculopathy secondary to cherubism is underestimated. As such, we feel that routine examination by an ophthalmologist be recommended in the management of a patient with cherubism.
This study was supported by an unrestricted grant from Research to Prevent Blindness, Inc, New York, NY.
A. J. Ahmadi, MD;
Goarik E. Pirinjian, DDS, MD;
Bryan S. Sires, MD, PhD
Seattle, Wash
Corresponding author and reprints: Bryan S. Sires, MD, PhD, University of Washington, Ophthalmology, Box 356485, Seattle, WA 98195-6485 (e-mail: bsires{at}u.washington.edu).
REFERENCES
1. Marck PA, Kudryk WH. Cherubism. J Otolaryngol. 1992;21:84-87.
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2. Hawes MJ. Cherubism and its orbital manifestations. Ophthal Plast Reconstr Surg. 1989;5:133-140.
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3. Jones WA. Familial multilocular cystic disease of the jaws. Am J Cancer. 1933;17:946-950.
4. Colombo F, Cursiefen C, Neukam FW, Holbach LM. Orbital involvement in cherubism. Ophthalmology. 2001;108:1884-1988.
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5. Peters WJ. Cherubism: a study of twenty cases from one family. Oral Surg Oral Med Oral Pathol. 1979;47:307-311.
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6. Mangion J, Rahman N, Edkins S, et al. The gene for cherubism maps to chromosome 4p16.3. Am J Hum Genet. 1999;65:151-157.
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7. Friedman E, Eisenbud L. Surgical and pathological considerations in cherubism. Int J Oral Surg. 1981;10:52-55.
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SECTION EDITOR: W. RICHARD GREEN, MD
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