[Graphite foreign body in the orbit].
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Biomedical subjects
Publications and source records attributed to H Offret.
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A report of a family in which three generations were affected by on autosomal dominant corneal dystrophy. The authors studied two fragments of a recurrence on a graft where they noted the presence of granular material. Histochemical studies were negative. Electron microscopy showed the presence of deposits of crystalline appearance resembling those of Groenouw type I dystrophy.
Ultrastructural study of two cases of persistent hyperplastic primary vitreous. Behind posterior lens capsule we find a connective tissue where fibroblasts present an intense activity. Numerous vessels and neuro-ectodermal tissue were noted.
Two cases of persistent hyperplastic primary vitreous have been managed by the vitreous cutter Sukon "Alternating" with a pars-plana approach.
Study of six cases of vitreous touch syndrom with histopathology of five buttoms of kératoplasty. Light and electron-microscopy demonstrate many alterations of Descemet's membrane, which is thickened, devided in sheets. In one specimen there was a retrocorneal fibrous membrane and "fibroblast like cells". These findings support the mechanism of endothelial fibrous metaplasia as the origin of the retrocorneal fibrous membrane during vitreous touch syndrom.
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A study was performed in two series of patients on whom lens extraction was done. Congenital cataracts were excluded from this study. In one series. the closure of the wounds was satisfactory; in the other, large anterior vitrectomy was carried out. The frequency of detachment (about 4%) seems to be approximately the same in the two series, but inflammatory signs and hypertony are more frequent when vitrectomy is not done.
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