Vitreous opacities in primary amyloid disease
نویسنده
چکیده
Severe loss of visual acuity due to vitreous opacities may result from haemorrhages, inflammatory and degenerative conditions, tumour cells, or amyloidthe last being rare (Duke-Elder, I969; Jaffe, I969). It is important, however, to recognize amyloid disease as being a cause of vitreous opacities, because most previously reported cases have been patients with familial amyloidosis, a systemic disease of protean manifestations with a poor prognosis. Sporadic cases of systemic amyloidosis with vitreous opacities have also been reported (see Table). Patients with systemic amyloid disease may initially present with visual symptoms due to vitreous opacities. These opacities usually have a characteristic appearance thus enabling the ophthalmologist to suggest the correct diagnosis. The purpose of this paper is to report three patients of primary amyloid disease, who initially presented to the ophthalmologist with slow deterioration of their visual acuity. The diagnosis was suggested by the appearance of the vitreous opacities and confirmed initially by conjunctival biopsy in two of the three cases and subsequently by histological examination of the vitreous in all three cases. To our knowledge, this is the first British report of vitreous opacities in primary amyloid disease.
منابع مشابه
Vitreous opacities in primary amyloid disease. A clinical, histochemical, and ultrastructural report.
Three patients who initially presented to the ophthalmologist with a history of gradual deterioration of visual acuity showed, on biomicroscopic examination, a linear meshwork of opacities in the vitreous attached to the posterior surface of the lens in the form of pseudopodia lentis. Amyloidosis of the vitreous associated with systemic amyloid disease was diagnosed because of the characteristi...
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We report a 61-year-old Japanese woman with transthyretin (TTR) Val33-related familial amyloid polyneuropathy (FAP). She presented with late-onset, vitreous involvement as the initial manifestation, slow development of polyneuropathy, cardiomyopathy, and severe autonomic failure without carpal tunnel syndrome. Liver transplantation was performed and her postoperative course was stable. Taken to...
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A 31-year-old woman thought to be suffering from a psychiatric illness was found to have peripheral and autonomic neuropathy, keratoconjunctivitis sicca and vitreous opacities. Her mother had died 10 years previously, aged 42 years from an undiagnosed illness with similar features. Histological proof of amyloidosis was obtained in both cases. This is the second report of familial amyloid neurop...
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Results Thirteen patients were female. The mean onset age was 58 years and average evolution time of the disease was 5, 6 years. All patients were TTR Met30 and 2 patients were compound heterozygous TTR met30 met119. Four patients had been submitted to liver transplant and nine were on Tafamidis treatment. Amyloid deposits on anterior lens surface were observed in 15 eyes (37,5%), scalloped pup...
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تاریخ انتشار 2004