中华眼科杂志
中華眼科雜誌
중화안과잡지
Chinese Journal of Ophthalmology
2013年
6期
507-513
,共7页
黄厚斌%魏世辉%李莹%王凤翔%姚毅%姜彩辉%阴正勤%张卯年%魏文斌
黃厚斌%魏世輝%李瑩%王鳳翔%姚毅%薑綵輝%陰正勤%張卯年%魏文斌
황후빈%위세휘%리형%왕봉상%요의%강채휘%음정근%장묘년%위문빈
副肿瘤综合征,眼%视网膜疾病%视神经疾病
副腫瘤綜閤徵,眼%視網膜疾病%視神經疾病
부종류종합정,안%시망막질병%시신경질병
Paraneoplastic syndromes,ocular%Retinal diseases%Optic nerve diseases
目的 探讨副肿瘤性视网膜视神经病变患者的临床特征及其临床意义.方法 系列病例研究.2006年10月至2012年3月解放军总医院眼科连续诊治副肿瘤性视网膜视神经病变患者8例(16只眼),行眼部照相、视觉电生理、荧光素眼底血管造影、相干光断层扫描、眼底自发荧光、视野、超声、MRI检查及腰穿脑脊液化验、副肿瘤综合征抗体检测等,并经门诊和(或)电话随访患者的病情变化和结局,分析其病变类型、临床表现及治疗结果等.结果 8例患者中,癌症相关性视网膜病变3例、双眼弥漫性葡萄膜黑色素细胞增生2例,副肿瘤性视神经病变3例.5例患者进行了副肿瘤综合征的抗体检测,3例结果阳性,2例结果阴性.8例患者中,肿瘤源自肺癌4例,源自侵袭性胸腺瘤、肾癌、急性淋巴细胞白血病、宫颈癌各1例.患者均主诉视物模糊或视力进行性下降,并有2例主诉视物遮挡,其他主诉包括眼前闪光感、炫目、复视、眼痛各1例.其中1例患者是由于进行性视力下降首诊于眼科后发现患有恶性肿瘤.在8例16只眼中,随访结束时无光感的6只眼,光感至0.05的5只眼,视力≥0.4的5只眼.5例患者接受糖皮质激素治疗,总体疗效不明显.结论 各型副肿瘤性视网膜视神经病变有其相应的临床表现,副肿瘤综合征尤其是双眼弥漫性葡萄膜黑色素细胞增生可能是一种转移前病变.
目的 探討副腫瘤性視網膜視神經病變患者的臨床特徵及其臨床意義.方法 繫列病例研究.2006年10月至2012年3月解放軍總醫院眼科連續診治副腫瘤性視網膜視神經病變患者8例(16隻眼),行眼部照相、視覺電生理、熒光素眼底血管造影、相榦光斷層掃描、眼底自髮熒光、視野、超聲、MRI檢查及腰穿腦脊液化驗、副腫瘤綜閤徵抗體檢測等,併經門診和(或)電話隨訪患者的病情變化和結跼,分析其病變類型、臨床錶現及治療結果等.結果 8例患者中,癌癥相關性視網膜病變3例、雙眼瀰漫性葡萄膜黑色素細胞增生2例,副腫瘤性視神經病變3例.5例患者進行瞭副腫瘤綜閤徵的抗體檢測,3例結果暘性,2例結果陰性.8例患者中,腫瘤源自肺癌4例,源自侵襲性胸腺瘤、腎癌、急性淋巴細胞白血病、宮頸癌各1例.患者均主訴視物模糊或視力進行性下降,併有2例主訴視物遮擋,其他主訴包括眼前閃光感、炫目、複視、眼痛各1例.其中1例患者是由于進行性視力下降首診于眼科後髮現患有噁性腫瘤.在8例16隻眼中,隨訪結束時無光感的6隻眼,光感至0.05的5隻眼,視力≥0.4的5隻眼.5例患者接受糖皮質激素治療,總體療效不明顯.結論 各型副腫瘤性視網膜視神經病變有其相應的臨床錶現,副腫瘤綜閤徵尤其是雙眼瀰漫性葡萄膜黑色素細胞增生可能是一種轉移前病變.
목적 탐토부종류성시망막시신경병변환자적림상특정급기림상의의.방법 계렬병례연구.2006년10월지2012년3월해방군총의원안과련속진치부종류성시망막시신경병변환자8례(16지안),행안부조상、시각전생리、형광소안저혈관조영、상간광단층소묘、안저자발형광、시야、초성、MRI검사급요천뇌척액화험、부종류종합정항체검측등,병경문진화(혹)전화수방환자적병정변화화결국,분석기병변류형、림상표현급치료결과등.결과 8례환자중,암증상관성시망막병변3례、쌍안미만성포도막흑색소세포증생2례,부종류성시신경병변3례.5례환자진행료부종류종합정적항체검측,3례결과양성,2례결과음성.8례환자중,종류원자폐암4례,원자침습성흉선류、신암、급성림파세포백혈병、궁경암각1례.환자균주소시물모호혹시력진행성하강,병유2례주소시물차당,기타주소포괄안전섬광감、현목、복시、안통각1례.기중1례환자시유우진행성시력하강수진우안과후발현환유악성종류.재8례16지안중,수방결속시무광감적6지안,광감지0.05적5지안,시력≥0.4적5지안.5례환자접수당피질격소치료,총체료효불명현.결론 각형부종류성시망막시신경병변유기상응적림상표현,부종류종합정우기시쌍안미만성포도막흑색소세포증생가능시일충전이전병변.
Objective To analyze the clinical characteristics of paraneoplastic retinopathy and optic neuropathy(PRON).Methods Case series study.Eight patients were enrolled from October 2006 to March 2012 visited in ophthalmology department,the People Liberation Army General Hospital.The patients were underwent a series of examinations,including fundus photography,visual electrophysiology,fundus fluorescein angiography,optic coherent tomography,fundus autofluorescent imaging,perimetry,ultrasonography,magnetic resonance imaging,spinal tap and cerebrospinal fluid test,paraneoplastic syndrome (PNS) antibody test.The patients were followed up in outpatient department and(or) by phone.The clinical manifestation,entity types,and treatment were analyzed.Results Of the eight patients,there were cancer associated retinopathy (CAR) 3 cases,bilateral diffuse uveal melanocytic proliferation (BDUMP) 2 cases and paraneoplastic optic neuropathy(PON) 3 cases.Five patients were detected the PNS antibodies and revealed three patients with positive results.As for the primary malignancy,four of the eight patients were lung carcinoma,others included invasive thymoma,kidney cancer,acute lymphocytic leukemia and cervical cancer,each for one case.All the patients complained vision blurring or progressive visual decrease.Other complaints included dark shadow in two patients,shimmering,dazzling,double vision and eye pain,each in one patient.One patient complained progressive decreased vision in both eyes prior to the diagnosis of lung cancer.Of the 16 eyes of the eight patients,there were six patients with no light perception vision,five from light perception to 0.05,and other five with no less than 0.4 vision,in the end of the follow up.Five patients were treated with steroid with unsatisfactory efficacy.Conclusions Each entity of PRON has its own clinical characteristics.PRON especially BDUMP may be a pre-metastatic disease.