Updated: Mar 18, 2009
Orbital and ocular changes associated with thyroid dysfunction were first reported by von Basedov in 1840, then Graves in 1935. Thyroid ophthalmopathy currently is recognized as the most common cause of proptosis (protrusion of the globe) in adults (see Image 1).
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Although not completely understood, the underlying pathophysiology of thyroid ophthalmopathy seems to be an autoimmune reaction directed toward orbital fibroblasts. Thyroglobulin, antithyroglobulin complexes, and other determinants common among orbital and thyroid antigens may initiate hypersensitivity reactions that result in the orbital changes in thyroid ophthalmopathy. Defects in immunoregulation allow B lymphocytes to produce autoantibodies that target extraocular muscles, orbital fat, and the lacrimal gland. Stimulation of orbital fibroblasts in these tissues results in production of hyaluronic acid, which increases the osmotic load of the tissues and results in passive swelling.2,3
The incidence of thyroid ophthalmopathy annually is 16 per 100,000 in women and 2.9 per 100,000 in men.
Thyroid ophthalmopathy is reported worldwide.
Although thyroid ophthalmopathy rarely causes death, its morbidity can be significant.
No racial predilection appears to exist for thyroid ophthalmopathy. Reports of thyroid ophthalmopathy exist worldwide, although exact genetic linkage varies among races.
Although the male-to-female ratio is 1:4, thyroid ophthalmopathy is more severe in men.
Thyroid ophthalmopathy causes enlargement of the extraocular muscles and surrounding orbital fat, resulting in proptosis. Muscular enlargement almost always is within the muscle belly, with sparing of the muscle tendon that inserts onto the globe, and often causes diplopia by restricting the globe's movement. Optic nerve compression can occur in the apex of the orbit, where the extraocular muscles originate. Treatment of thyroid ophthalmopathy involves excision of the orbital fat and expansion of orbital volume by fracturing and/or removing the orbital walls. Acute exacerbations of thyroid ophthalmopathy may be treated with either corticosteroids or radiation therapy.
Proptosis is the most common sign of thyroid ophthalmopathy and is caused by enlargement of the extraocular muscles, as well as the orbital fat. The most commonly involved extraocular muscles are (from most frequent to least frequent) the inferior rectus, medial rectus, superior rectus, oblique muscles, and lateral rectus. Upper and lower eyelid retraction also is a common feature of thyroid eye disease.
Clinical exacerbations of thyroid ophthalmopathy can occur and are characterized by marked worsening of proptosis, painful myositis, and significant chemosis and vascular engorgement within the orbit. Immediate treatment with corticosteroids often is required to prevent or minimize associated compressive optic neuropathy.
Orbital ultrasonography is the most convenient examination for the diagnosis of thyroid ophthalmopathy, because it can be performed quickly and with a high degree of confidence. High reflectivity and enlargement of the extraocular muscles are assessed easily, and serial sonographic examinations can also be used to assess progression or stability of the ophthalmopathy.
Computed tomography (CT) scanning is an excellent imaging modality for the diagnosis of thyroid ophthalmopathy. In addition to allowing visualization of the enlarged extraocular muscles, CT scans provide the surgeon with depictions of the bony anatomy of the orbit when an orbital decompression is required. Magnetic resonance imaging (MRI) also provides excellent imaging of the orbital contents, without the radiation exposure associated with CT scan studies. MRI provides better imaging of the optic nerve, orbital fat, and extraocular muscle, but CT scans provide better views of the bony architecture of the orbit.
The primary limitations of orbital ultrasonography are lack of visualization of the bony orbital architecture and inability to image the orbital apex. CT scanning provides excellent studies; however, cost and radiation exposure limit their use for serial examinations. MRI can assess the amount of fat within the orbit, but CT scans provide better views of the bony anatomy and are less expensive.
Orbital myositis (inflammatory pseudotumor of the orbit)
Cavernous sinus thrombosis
Histiocytosis X
Lacrimal gland tumor
Orbital varices
Cavernous hemangioma of the orbit
Conventional radiographs are not useful in the diagnosis of thyroid ophthalmopathy, because bony abnormalities usually are not associated with the disease.
The degree of confidence is poor. Radiographs cannot determine the amount of extraocular muscle enlargement, degree of optic nerve compression, or presence of other orbital processes that may mimic thyroid ophthalmopathy. Perform orbital ultrasonography, CT scanning, or MRI instead.
CT scanning provides excellent visualization of the extraocular muscles and intraconal fat, as well as the orbital apex. Enlargement of the muscles occurs almost uniformly within the muscle belly (see Images 3-4), and thickening is usually greater than 4 mm. The tendinous insertion (which is easily visualized in axial sections) usually is not enlarged. Prominent intraconal fat can also result in proptosis (see Image 5).
The degree of confidence is high. An additional test rarely is required for the diagnosis of thyroid ophthalmopathy. Orbital ultrasonography also can provide the diagnosis with a high degree of confidence, but cost and convenience considerations make ultrasonography more useful when serial imaging is required.
Orbital myositis often can mimic the clinical appearance of thyroid ophthalmopathy. This condition most often is unilateral, and the tendinous insertions of the extraocular muscles also are enlarged. Metastatic tumors to the extraocular muscles also may mimic thyroid eye disease, although they are usually associated with other orbital and bony metastases. However, other etiologies should be considered in the presence of isolated lateral rectus muscle enlargement, because this is almost never seen in thyroid orbitopathy.
Similar to CT scan studies, MRI also provides excellent imaging of the extraocular muscles, their insertions, and the anatomy of the orbital apex (see Image 6).
In addition, the amount of fat within the orbit and imaging of the optic nerve can be assessed and localized on MRI better than on CT scans. Typically, however, MRI is not the ideal imaging modality because of the associated increased cost.4,5,6
Because of the significant amount of fat present within the orbit, fat-suppression techniques are utilized in its evaluation, particularly if MRI contrast agents are administered. Fat normally appears bright on both T1-weighted and fast T2-weighted pulse sequences; however, fat suppression significantly reduces the signal from fat, thereby rendering it dark on MRIs. This greatly improves lesion detection by increasing the contrast between the orbital fat and pathologic processes. With MRI contrast administration, enhancing lesions become much more conspicuous with fat suppression during T1-weighted imaging. Likewise, in evaluating tumor or inflammatory processes with higher water content, these abnormalities become easily visible with fat suppression during fast T2-weighted sequences.
The MRI signal intensity of the enlarged extraocular muscles is usually isointense on T1-weighted images and isointense to minimally hyperintense on T2-weighted images. High intensity in the extraocular muscle on T1-weighted images is occasionally seen, which is consistent with fatty infiltration. This finding can aid in differentiating thyroid orbitopathy from pseudotumor.
Increased T2 signal in the extraocular muscles is likely caused by increased water content. Patients with elevated T2 relaxation times have increased response to anti-inflammatory treatment (this is similar to octreotide accumulation [see Nuclear Medicine section]).
The degree of confidence is high. Similar to CT scanning, MRI usually can provide the diagnosis of thyroid ophthalmopathy with or without optic nerve compression. Additional testing usually is not required if an MRI study already has been obtained.
MRI may be better than CT scanning in identifying other causes of proptosis, such as orbital tumors.
Orbital ultrasonography is excellent for the diagnosis of thyroid ophthalmopathy, and medium to high internal reflectivity of the extraocular muscles, as well as enlargement of the muscle belly, is characteristic. The tendinous insertion of the extraocular muscle also can be visualized easily. Patients with thyroid ophthalmopathy show lower peak-systolic and end-diastolic velocities that may be appreciated with Doppler imaging. Visualization of the orbital apex is difficult with orbital ultrasonography, and CT scanning or MRI may be preferred when compression of the optic nerve is suspected.7
The degree of confidence is high. Additional examinations to diagnose thyroid ophthalmopathy are not needed if the characteristic high reflectivity and enlargement of the extraocular muscles with sparing of the tendinous insertion are present on sonograms. However, to better visualize the apex of the orbit for evidence of optic nerve compression, CT scanning or MRI may be required if warranted by the clinical presentation.
Orbital myositis is characterized by high reflectivity and enlarged extraocular muscle bellies when examined with ultrasonography. However, in orbital myositis, the tendinous insertion is enlarged, which differentiates this condition from thyroid ophthalmopathy.
Although not clinically useful in the diagnosis of thyroid ophthalmopathy, functional studies such as positron emission tomography (PET) scans or somatostatin-receptor scintigraphy (SRS) may assess disease activity. Orbital infiltration with mononuclear cells in thyroid ophthalmopathy can be identified by receptor imaging with octreotide, a radiolabeled somatostatin analogue.
Patients with active thyroid ophthalmopathy show higher octreotide uptake and may respond better to treatments such as corticosteroids or radiation therapy. Patients with inactive disease, however, do not respond to these treatments. In the future, nuclear medicine testing may determine whether stability of the orbital disease has been achieved before proceeding to surgical decompression.8,9
Patients with thyroid ophthalmopathy often present when their disease is no longer active. PET scans or somatostatin-receptor scintigraphy (SRS) in these patients is not informative, and alternative imaging methods (ultrasonography or CT scanning) are required.
Other orbital inflammatory processes also may result in increased uptake during functional imaging.
Angiography typically is not used in the diagnosis or management of thyroid ophthalmopathy. Enlarged orbital vessels with increased blood-flow velocities may be present.
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thyroid ophthalmopathy, thyroid eye disease, Graves disease, Graves' disease, Graves ophthalmopathy, thyrotoxic ophthalmopathy, thyrotoxic exophthalmos, thyroid-associated ophthalmopathy, endocrine exophthalmos
Michael T Yen, MD, Associate Professor of Ophthalmology, Department of Ophthalmology, Division of Ophthalmic Plastic, Lacrimal, and Orbital Surgery, Cullen Eye Institute, Baylor College of Medicine
Michael T Yen, MD is a member of the following medical societies: American Academy of Ophthalmology, American Society of Cataract and Refractive Surgery, American Society of Ophthalmic Plastic and Reconstructive Surgery, and Association for Research in Vision and Ophthalmology
Disclosure: Nothing to disclose.
Rudolph Lin, MD, Chief of Radiology, Department of Radiology, St. Elizabeth Hospital
Rudolph Lin, MD is a member of the following medical societies: American College of Radiology, American Medical Association, American Roentgen Ray Society, and Radiological Society of North America
Disclosure: Nothing to disclose.
Kimberly G Yen, MD, Assistant Professor of Ophthalmology, Department of Ophthalmology, Cullen Eye Institute, Baylor College of Medicine
Kimberly G Yen, MD is a member of the following medical societies: Association for Research in Vision and Ophthalmology
Disclosure: Nothing to disclose.
David S Levey, MD, PhD, Orthopedic/Spine MRI TeleRadiologist, Radsource, LLC
David S Levey, MD, PhD is a member of the following medical societies: American Roentgen Ray Society, Radiological Society of North America, and Texas Medical Association
Disclosure: Nothing to disclose.
Bernard D Coombs, MB, ChB, PhD, Consulting Staff, Department of Specialist Rehabilitation Services, Hutt Valley District Health Board, New Zealand
Disclosure: Nothing to disclose.
C Douglas Phillips, MD, Professor, Departments of Radiology, Neurosurgery, and Otolaryngology, University of Virginia Health Sciences Center
C Douglas Phillips, MD is a member of the following medical societies: American College of Radiology, American Medical Association, American Society of Head and Neck Radiology, American Society of Neuroradiology, Association of University Radiologists, and Radiological Society of North America
Disclosure: Nothing to disclose.
Robert M Krasny, MD, Consulting Staff, Department of Radiology, The Angeles Clinic and Research Institute
Robert M Krasny, MD is a member of the following medical societies: American Roentgen Ray Society and Radiological Society of North America
Disclosure: Nothing to disclose.
Eugene C Lin, MD, Consulting Radiologist, Virginia Mason Medical Center; Clinical Assistant Professor of Radiology, University of Washington School of Medicine
Eugene C Lin, MD is a member of the following medical societies: American College of Nuclear Medicine, American College of Radiology, Radiological Society of North America, and Society of Nuclear Medicine
Disclosure: Nothing to disclose.
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