On imaging, it is characterised by bilateral and symmetrical enlargement of the extraocular muscle bellies. The typical distribution is: inferior rectus > medial rectus > superior rectus, with sparing of the tendinous insertions.
The demographics of thyroid associated orbitopathy reflects that of patients with thyroid disease and is therefore more frequently seen in women. Although Graves disease is the most common cause, Hashimoto thyroiditis has also been implicated. It may precede the onset of abnormal thyroid function, occur concurrently, or commence following its onset.
- lid retraction
- proptosis, with resultant chemosis and corneal dryness and ulceration
- optic nerve compression, potentially leading to blindness
- diplopia 1
- hypoglobus: uncommon
Thyroid associated orbitopathy is characterised by enlargement of the extra-ocular muscles as well as the increase in the orbital fat volume 1. While the exact mechanism is unknown, antibodies to thyroid stimulating hormone (TSH) appear to cross react with antigens in the orbit resulting in infiltration by activated T lymphocytes 3, with subsequent release of inflammatory mediators.
The muscles are infiltrated with inflammatory cells (lymphocytes, macrophages, plasma cells, and eosinophils), and increased mucopolysccaride deposition. In longstanding cases, increased collagen deposition leads to fibrosis 1.
- inferior rectus
- medial rectus
- superior rectus
- lateral rectus
Increase in orbital fat volume is a result of venous congestion from the compression of the superior ophthalmic vein by the enlarged muscles and/or intrinsic adipose inflammation.
Due to its widespread availability and rapid image acquisition, the diagnosis is often first made on CT. Intravenous contrast, although ideal, is not necessary, as the differing densities of orbital fat and muscle allow for adequate delineation of the orbital contents.
- draw a line between the anterior tips of the zygomatic bones and measure the distance between the line and the posterior part of the eyeball. Normal distance is greater than 10±1.7mm 6; a reduced distance indicates exopthalmos
- extraocular muscle enlargement and fatty attenuation
- characteristic order of muscle involvement can be remembered by the mnemonic I'M SLOW
- bilateral (76-90%) and symmetric (70%) involvement is typical
- the anterior tendon is typically spared (although it can be involved in acute cases), with the swelling largely confined to the muscle belly
- this appearance if often referred to as 'coke bottle' in nature (coca-cola bottle sign), given its resemblance to the classic Coca-ColaTM bottle
- enlargement of the muscle belly is usually accompanied by reduced attenuation representing fatty infiltration 7
- the size of the muscles correlates with both the severity of disease and the risk of optic nerve compression 7
- increase in retro-ocular orbital fat
The greater the extraocular muscle bulk (especially medial rectus bulk nearer to the apex) and the longer and narrower the bony orbit, the more crowded the orbital apex will become. Apical crowding could result in optic nerve dysfunction/optic neuropathy due to optic nerve compression 1,2.
Other rarer signs include 7:
- enlargement of the lacrimal glands (lymphocytic infiltration)
- anterior displacement of the orbital septum
Evaluation with MRI may be useful due to improved soft tissue contrast and multi-planar capabilities. MR prevents ionising radiation to orbits and corresponding increased risk of radiation-induced cataracts. Location and involvement of the ocular muscles generally follows the described CT appearances. Specific MRI sequences findings may include:
- T1: isointense to the other facial muscles, or fatty infiltration
- T2: increased signal intensity may be seen due the inflammatory process
- T1 C+ (Gd): enhancement may be present
Treatment and prognosis
Although in many instances the disease is self-limiting, spontaneously improving within 2-5 years 3, discomfort, cosmetic issues, the risk of corneal ulceration, and optic nerve compression often require treatment. Options include:
- supportive, steroids
- radiotherapy 3
- surgical decompression
General imaging differential considerations include:
- 1. Glatt HJ. Optic nerve dysfunction in thyroid eye disease: a clinician's perspective. Radiology. 1996;200 (1): 26-7. Radiology (citation) - Pubmed citation
- 2. Chan LL, Tan HE, Fook-chong S et-al. Graves ophthalmopathy: the bony orbit in optic neuropathy, its apical angular capacity, and impact on prediction of risk. AJNR Am J Neuroradiol. 2009;30 (3): 597-602. doi:10.3174/ajnr.A1413 - Pubmed citation
- 3. Cockerham KP, Kennerdell JS. Does radiotherapy have a role in the management of thyroid orbitopathy? View 1. Br J Ophthalmol. 2002;86 (1): 102-4. Br J Ophthalmol (link) - Free text at pubmed - Pubmed citation
- 4. Birchall D, Goodall KL, Noble JL et-al. Graves ophthalmopathy: intracranial fat prolapse on CT images as an indicator of optic nerve compression. Radiology. 1996;200 (1): 123-7. Radiology (abstract) - Pubmed citation
- 5. Nugent RA, Belkin RI, Neigel JM et-al. Graves orbitopathy: correlation of CT and clinical findings. Radiology. 1990;177 (3): 675-82. Radiology (abstract) - Pubmed citation
- 6. Keats TE, Sistrom C. Atlas of Radiologic Measurement. Mosby. (2001) ISBN:0323001610. Read it at Google Books - Find it at Amazon pp. 92-95
- 7. Parmar H, Ibrahim M. Extrathyroidal manifestations of thyroid disease: thyroid ophthalmopathy. Neuroimaging Clin. N. Am. 2008;18 (3): 527-36, viii-ix. doi:10.1016/j.nic.2008.03.003 - Pubmed citation
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