双眼先天性黄斑缺损一例

患者男 29岁自幼双眼视物不清.加重两年于2008年8月3日就诊.查体:全身发育未见异常.无手足畸形.眼部检查:视力:右眼0.06,左眼0.04.双眼前节无异常,视盘界清,色淡红,C/D约0.3,双眼黄斑区均可见一直径约3PD大小的近圆形脉络膜缺损区,边界清晰,缺损区内可见不规则散在的色素沉着,视网膜血管走行正常,底部可透见较粗大的脉络膜血管.     

双眼先天性黄斑缺损一例报告

先天性黄斑缺损临床较为少见。一般单眼发病,双眼者罕见。现将我院近期所遇一例双眼先天性黄斑缺损报道如下:患者女13岁因双眼自幼视物不清近半年增重于2005年3月7日来我院就诊。既往无眼病史,父母非近亲结婚,家族无同类患者,发育正常,无指趾畸形。视力:右0.08,左0.04,双眼前节无异常发现。双眼底:视乳头边界清晰,色正常,黄斑区可见直径约4PD大小横椭圆形脉络膜缺损区,边界清晰,缺损区内视网膜血管走行正常,无间断,底部可透见部分脉络膜大血管并见不规则散在色素沉着斑(图1)。荧光血管造影检查:黄斑缺损区无脉络膜背景荧光,可见部分脉络膜…     

双眼先天性巨大黄斑缺损一例

患者男,15岁,因发现双眼眼视力差9年来我院门诊就诊.患者为足月顺产,G1P1,妊娠期无异常;家族中无此类疾病.否认眼外伤史.     

双眼先天性黄斑缺损

患者女性,12岁.自幼双眼视力差,于2010年12月5日来广州市番禺区中心医院眼科就诊.既往眼部未给予特殊检查和治疗,无其他疾病史,父母非近亲结婚,母亲孕期无感染病史,家族中无类似患者.全身体检:一般状况良好,发育正常,无指趾畸形.眼部检查:视力左眼为0.05,右眼为0.1,双眼均无法矫正;双眼前节检查来见明显异常;眼底检查情况见精粹图片1.     

双眼先天性黄斑缺损

先天性黄斑缺损,系属先天性视网膜脉络膜的发育畸形,临床较少见,国内外文献报导亦不多。我科曾遇见一例,报告如下。     

双眼先天性黄斑缺损

患者女 ,2 2岁。因左眼外斜视于 2 0 0 3年 6月来我院就诊。自诉从懂事起双眼视力差 ,伴左眼外斜视。既往无其他眼病史 ,父母非近亲结婚 ,母亲孕期有无感染病史不清楚。全身检查 :一般情况好 ,发育正常 ,无指趾畸形。视力右眼 0 .15 ,左眼 0 .12 ,经复方托品酰胺散瞳后 ,矫正视力右眼 0 .15→ - 0 .75 DS=0.2 ,左眼 0 .12→ - 1.5 0 DS=0 .15 ,33cm照影左眼 - 2 0°。双眼球各方向运动无受限 ,双眼前节正常 ,屈光间质透明。双眼底视盘色正常 ,边界清楚 ,黄斑区可见横椭圆形 5 .3PD× 4 .3PD大小的脉络膜毛细血管缺损区 ,边界清楚 ,围绕…     

双眼先天性黄斑缺损1例

0引言先天性黄斑缺损是指黄斑区视网膜和脉络膜的先天性发育异常,常单眼发病,双眼罕见,多数属于常染色体显性遗传,少数为隐性遗传,也有部分散发。目前,黄斑缺损和发育异常真正的原因尚不清楚。该病可累及双眼,自幼双眼视力差,一般病情稳定多年无发展。临床较少见,近期我们遇到1例,现报告如下。1病例报告患者,男,23岁,因自幼双眼视物模糊来我院就诊。患者否认早产,外伤,眼病病史及家族史。PE:Vod=0.1,Vos=0.12,矫正无提高。双眼压正常,双眼角膜透明,前房深浅正常,瞳孔等大等圆居中,晶状体透明,视乳头清晰,双眼黄斑区边界清楚,类圆形4PD×4PD大小脉络膜缺损,中央可透见部分脉络膜大血管,散在     

双眼先天性黄斑缺损1例

患者男，40岁。主诉：自幼双眼视力不佳。无家族遗传史。检查：右眼视力为4．3，左眼视力为4．1。双眼球无突出及凹陷，双眼前节正常。双眼底：视乳头额下方，距视乳头IPD，相当于黄斑区域可见圆形黄斑缺损区，左眼约ZPD，右眼约trPD。诊断：双眼黄斑缺损（色素型人一’””————”q－”——～’”””””“”””””“mp”“””荧光眼底血管造影检查：右眼黄斑区有一直径约了m圆形黄斑缺损区，除预测边界有切迹，余边界清晰，圆形区内荧光强弱不均，弱荧光区域为色素增殖所致形成荣光遮蔽，并还可见到少许脉络膜粗大血管。左眼黄…     

双眼先天性黄斑缺损1例

先天性黄斑缺损是指黄斑区视网膜和脉络膜的先天性发育异常,常单眼发病,双眼罕见,多数属于常染色体显性遗传,少数为隐性遗传,也有部分散发。目前,黄斑缺损和发育异常真正的原因尚不清楚。该病可累及双眼,白幼双眼视力差,一般病情稳定多年无发展。临床较少见,近期我们遇到1例,现报告如下。     

双眼先天性黄斑缺损两例

先天性黄斑缺损是严重影响患者中心视力的眼底先天性异常,临床较少见,大多为单眼,偶有双眼.笔者遇2例男性双眼受累患者,现报告如下. 例1,29岁,因自幼双眼视力差,于2009年3月30日就诊我院.既往无眼外伤及手术史,家族中无近亲结婚及类似史,母亲孕期感染史不明确.     

Bilateral Macular Edema in a Patient Treated with Tamoxifen: A Case Report and Review of the Literature

We present a case of a 41-year-old female patient with progressive bilateral visual loss. On examination, her best corrected visual acuity (BCVA) in her right eye was 3/10 and her BCVA in her left eye was 2/10. Fundus and optical coherence tomography examination revealed severe bilateral macular edema. She had been diagnosed with breast cancer 6 years ago and was receiving tamoxifen at a dosage of 20 mg/day ever since. Tamoxifen therapy was discontinued, and the patient received 250 mg of acetazolamide three times a day for a period of 1 month. Both foveae regained their normal contour within 2 months, and her vision was restored to 10/10 BCVA 3 months later. To our knowledge, this is the first case reported where bilateral intraretinal macular edema is the only retinal manifestation in a patient on oral tamoxifen.Key words: Tamoxifen retinopathy, Tamoxifen therapy, Macular edema     

Bilateral Complete Isolated Cryptophthalmos: A Case Report

Cryptophthalmos is a condition of congenital eyelid malformation most commonly accompanied by syndactyly, urogenital anomalies, and cognitive impairments as in Fraser syndrome. We report on a patient with characteristic features consistent with autosomal dominant bilateral complete isolated cryptophthalmos. This patient represents only the sixth documented case of bilateral complete isolated cryptophthalmos. Defining characteristics of this variety are discussed, including bilateral central dimpling over the globes, normal eyebrow growth, and the absence of cognitive impairment. We introduce phenotypic features that distinguish bilateral isolated cryptophthalmos from other forms and discuss its relatively favorable prognosis.     

Best Macular Dystrophy in a Nigerian: A Case Report

Best macular dystrophy is reported to be rare in Africans. It is a hereditary disease that starts in childhood and progresses through some stages before visual symptoms occur. This case report presents a 43-year-old Nigerian with the disease and stresses the importance of regular eye exams of patients and relatives to detect changes such as choroidal neovascular membrane amenable to treatment.Key Words: Best macular dystrophy, Choroidal neovascular membrane, Retina, Nigerian, Tunnel vision