摘要:

Alkali treatment of whole cornea produces a high molecular weight polypeptide causing a respiratory burst in neutrophils. The current study was conducted to determine if this stimulant could be elicited from cultured or scraped corneal cells (epithelium, keratocytes, or endothelium). Fresh or previously frozen epithelium, endothelium, and stroma were isolated from bovine eyes, alkali treated, and tested for the presence of the respiratory burst stimulant. The same procedure was performed on cultured bovine epithelium, keratocytes, and endothelium. To determine if the stimulant is specific to corneal cells, the component parts of human blood (cellular and extracellular) were separated, treated with alkali, and tested individually. Activation of the respiratory burst of polymorphonuclear leukocytes (PMNs) was used as a marker for the presence of the stimulant. All alkali-degraded cell samples, except red blood cells, produced a respiratory burst when added to viable PMNs. Alkali-treated plasma induced weak stimulation. Bovine corneal epithelium was alkali-treated and separated by high-performance liquid chromatography (HPLC) according to molecular size. The stimulant was shown to have a high molecular weight by its recovery in HPLC fraction number 7. These results demonstrate that the PMN stimulant originates from cells. This PMN stimulant is proposed as an inflammatory mediator in the alkali-injured cornea.

ISSN:0277-3740    

出版商:OVID    

年代:1993

数据来源: OVID

摘要:

Recent studies of diabetic corneal epitheliopathy have shown that diabetic aphakic patients suffer from an enlarged cell area. This study focuses on a 41-year-old diabetic woman whose mean cell area before treatment was 1,101 ± 275 μm2. Seven months after treatment it decreased to 723 ± 253 μm2. This case shows that through the application of topical aldose reductase inhibitor, the mean cell area in diabetic aphakic patients can decrease toward a normal number.

ISSN:0277-3740    

出版商:OVID    

年代:1993

数据来源: OVID

摘要:

Congenital absence of Bowman's layer has been described in Peters' anomaly, sclerocornea, and osteogenesis imperfecta type II. More commonly, Bowman's layer is absent secondary to inflammatory or degenerative processes of the cornea. We present three cases of bilateral absence of Bowman's layer in otherwise unremarkable corneas that were unassociated with other ocular or systemic abnormalities. In a fourth case, similar absence of Bowman's layer was present in a patient with osteogenesis imperfecta type III. In all four cases, the absence of Bowman's layer was unassociated with any evidence of scarring or inflammation. By electron microscopy, the stroma was composed of regularly arranged collagen fibers with a uniform fiber diameter throughout. In the case of osteogenesis imperfecta type III, there was mild irregularity of the anteriormost stroma. The lack of inflammation or scarring in these four cases lead us to conclude that they represent a true congenital absence, or agenesis, of Bowman's layer.

ISSN:0277-3740    

出版商:OVID    

年代:1993

数据来源: OVID

摘要:

A rare bilateral severe keratomalacia occurred in an emaciated alcoholic, 57-year-old white man with acute necrotic pancreatitis. The patient had a 10-year history of chronic alcoholism. Laboratory and clinical findings were consistent with the diagnosis of a fat malabsorptive and malnutrition syndrome secondary to chronic and acute alcoholic pancreatitis. Visual acuity of both eyes was limited to light perception. Bilateral corneal necrosis after acute pancreatitis has not previously been reported.

ISSN:0277-3740    

出版商:OVID    

年代:1993

数据来源: OVID

摘要:

Ophthalmic involvement may be noted in ≤ 58% of Wegener's granulomatosis cases, scleritis being one of the most frequent and potentially devastating manifestations. Cytotoxic immunosuppressive drug therapy is effective treatment for this disorder but potentially highly toxic. Recent uncontrolled and anecdotal reports have suggested a possible therapeutic role for a much less toxic agent, trimethoprim/sulfamethoxazole, in limited Wegener's granulomatosis. We report a patient who had a conjunctival nodule and scleritis. Biopsy of the nodule suggested Wegener's granulomatosis, confirmed serologically with serum anti-neutrophil cytoplasmic antibody (ANCA) testing. Treatment with oral trimethoprim/ sulfamethoxazole was successful. Clinical response was paralleled by normalization of serial anti-neutrophil cytoplasmic antibody titers. This case is the first well-documented ophthalmologic report of limited Wegener's granulomatosis responding to trimethoprim/sulfamethoxazole and adds to the body of literature suggesting a potential role for this drug in selected cases of limited Wegener's granulomatosis.

ISSN:0277-3740    

出版商:OVID    

年代:1993

数据来源: OVID

摘要:

While largely successful, the use of a conjunctival autograft in the exposed scleral bed following a pterygium excision can result in postoperative complications. We report two cases of a previously undescribed complication: subconjunctival fibrosis at the harvest site of the graft. In one case, the fibrosis caused an asymptomatic, purely cosmetic defect; however, in the other case, the scar tissue constricted the extraocular movement with resultant diplopia. We call attention to this complication as it can affect visual function; we discuss its management and prevention.

ISSN:0277-3740    

出版商:OVID    

年代:1993

数据来源: OVID

ISSN:0277-3740    

出版商:OVID    

年代:1993

数据来源: OVID