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Imaging in Graves’ Ophthalmopathy

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Thyroid Eye Disease

Part of the book series: Endocrine Updates ((ENDO,volume 14))

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Abstract

Graves’ ophthalmopathy (GO) is an autoimmune condition of the orbit which is closely associated with Graves’ hyperthyroidism, though either condition may exist without the other. It may antedate, coincide with or follow hyperthyroidism (15). Assessment of the frequency of the association depends on the method used for detecting GO; with sensitive methods sub clinical GO can be demonstrated in 60–70% of patients with hyperthyroidism, whereas it is clinically apparent and moderately severe in about 10%. The clinical features of the disorder vary from a mild grittiness of the eyes to severe diplopia, loss of vision and disfiguring proptosis. The pathogenesis is poorly understood, and the available methods for prevention and treatment are far from ideal. The most obvious pathological change within the orbit is the enlargement of extra ocular muscles (6). In most cases microscopy reveals that the muscle fibers are preserved and the increase in muscle bulk reflects changes in the connective tissue: fibroblasts are very numerous, there is lymphocyte infiltration (812), an excessive deposition of collagen and of glycosaminoglycans (GAG) which lead to interstitial edema. A role for cytokines in GO (13) seems likely: it may be that the autoimmune response evokes the local production within the orbit of cytokines which cause fibroblast stimulation and hence the production of collagen and GAGs (1418). The muscles most frequently affected are the medial and inferior recti. Functionally the effect is of tightness or contraction of the muscles, and thus the patient may experience difficulty with upward or lateral gaze.

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Kahaly, G.J., Müller-Forell, W., Förster, G.J., Pitz, S., Rösier, H.P., Mann, W.J. (2001). Imaging in Graves’ Ophthalmopathy. In: Bahn, R.S. (eds) Thyroid Eye Disease. Endocrine Updates, vol 14. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-1447-3_9

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