trichiasis/amyloid

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مقالاتالتجارب السريريةبراءات الاختراع

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14 النتائج

[A case of corneal lactoferrin amyloidosis secondary to trichiasis].

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OBJECTIVE A case of corneal lactoferrin amyloidosis secondary to trichiasis is reported. METHODS A 30-year-old male suffered from trichiasis with an elevated gray whitish lesion just under the center of the cornea in his right eye. The lesion had an irregular surface. METHODS We excised the corneal

Secondary localized amyloidosis of the cornea caused by trichiasis.

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A 43-year-old woman complained of gradual visual impairment, foreign body sensation, and a white mass in the right eye. Trichiasis and corneal excrescence were observed. A systemic examination revealed no concurrent disease; the family history was noncontributory. A lamellar keratoplasty was

[A histopathological study of corneal amyloidosis secondary to trichiasis].

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We present a case of secondary corneal amyloidosis whose etiological mechanism was investigated by immunohistochemistry and electron microscopy. A 48-year-old woman had suffered from trichiasis in the right eye for 35 years, and developed secondary corneal amyloidosis, a phenomenon previously

Localized amyloidosis of the cornea secondary to trichiasis: clinical course and pathogenesis.

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OBJECTIVE To present four cases of localized corneal amyloidosis secondary to trichiasis and to discuss its pathogenesis. METHODS Medical and pathologic records of four patients with corneal amyloidosis secondary to trichiasis were reviewed retrospectively. Two patients underwent trichiasis surgery

Lattice dystrophy-like localized amyloidosis of the cornea secondary to trichiasis.

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OBJECTIVE To report a case of stellate and branching linear corneal stromal amyloid deposits secondary to trichiasis and the use of molecular genetic analysis to exclude lattice corneal dystrophy. METHODS Case report and review of the literature. A 30-year-old man with a history of chronic ocular

[Corneal amyloidosis complicated by trichiasis--immunohistochemical identification of the amyloid light chain protein].

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OBJECTIVE To identify the amyloid protein of the corneal amyloidosis complicated by trichiasis. METHODS The two patients were 41-year-old and 38-year-old women with trichiasis. They had gelatinous drop-like corneal change in hemilateral eye. The lesion was excised and examined by light and electron

Corneal amyloidosis complicated by trichiasis. Immunohistochemical identification of the amyloid light chain protein

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Purpose: To identify the amyloid protein of the corneal amyloidosis complicated by trichiasis.Methods: The two patients were 41-year-old and 38-year-old women with trichiasis. They had gelatinous drop-like corneal change in the hemilateral eye. The lesion was excised and examined by light and

Classification of secondary corneal amyloidosis and involvement of lactoferrin.

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OBJECTIVE To classify secondary corneal amyloidosis (SCA) by its clinical appearance, to analyze the demographics of the patients, and to determine the involvement of lactoferrin. METHODS Retrospective, observational, noncomparative, multicenter study. METHODS Twenty-nine eyes of 29 patients

A novel localized amyloidosis associated with lactoferrin in the cornea.

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We report a novel localized amyloidosis associated with lactoferrin. To elucidate the precursor protein of corneal amyloidosis associated with trichiasis, we analyzed amyloid deposits from three patients by histopathology and biochemistry. Amyloid deposits showed immunoreactivity, confirmed by

Lactoferrin Glu561Asp facilitates secondary amyloidosis in the cornea.

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OBJECTIVE To elucidate the pathogenic mechanism of amyloid formation in corneal amyloidosis with trichiasis. METHODS Ophthalmological examination was performed in nine patients to determine secondary corneal amyloidosis with trichiasis. Congo red staining and immunohistochemistry using anti-human

[Analyses of pathogenesis and therapeutic approaches for hereditary amyloidosis].

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Amyloidosis is a disorder of protein metabolism in which normally soluble autologous proteins are deposited in tissues as abnormal insoluble fibrils, causing structural and functional disruptions. We have recently identified the novel localized amyloidosis accompanied by trichiasis. The precursor

Conjunctival amyloidosis: is it related to trachoma?

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Due to presence of trachoma in a large percentage of cases of conjunctival amyloidosis, trachoma has been blamed for causing secondary localized amyloidosis. However, there is no study to demonstrate evidence of amyloidosis in tarsoconjunctival specimens of trachomatous lids. 50 eyes of 35 patients

[Corneal tumor secondary to trichiasis].

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A rare lesion of secondary amyloidosis of the cornea caused by trichiasis is reported. A 33-year-old Asian woman presented with progressive decrease of visual acuity of the right eye evolving over several years, combined with the growth of a lower budding, gelatinous, pink corneal mass located next

Findings of secondary corneal amyloidosis with ultrahigh-resolution optical coherence tomography.

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OBJECTIVE To describe observations by ultrahigh-resolution optical coherence tomography (OCT) in a secondary corneal amyloidosis (SCA) patient with histological analysis of excised tissue. A unique finding under OCT of her fellow eye is also described. METHODS A 39-year-old female had suffered from

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