​ Eye Cancer

Disease Overview

eyecarcinomais发lifeineyeinternaloreyeAdnexatissueofmalignant tumor,incidencerelativelylow,butsevereVision-threateningandlifeLife.includingprimaryeyeinternaltumor(such asretinoblastoma、uveal melanoma)andmetastaticeyeinternaltumor(such aschoroidal metastatic carcinoma)。good发regionpositionasRetina, uvea(Iris, ciliaryconditionbody, Choroid)andeyeAdnexa(eyelid, Conjunctiva)。differenttypeeyecarcinomaof发diseaseyearAge differencedifferentrelativelylarge,retinoblastomamore见inchildren,uveal melanomamore见inadults。early-stageDiagnosisandtreatmentforprognosis至closeimportant。


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Major Causes

Genetic factors:retinoblastomaandRB1gene突changeClosely relatedrelated,approximately40%patientsasgenetictype,canFrom parentsgenetic。

UV exposure:long-term紫external线radiationiseyelidskincarcinoma, Conjunctivasquamous cell carcinomaofimportantrisk factor。

Viral infection:HPVinfectionandConjunctiva,eyelidsquamous cell carcinomarelated;EBdiseasetoxinandlymphatictumorrelated。

Melanocyte abnormalities:uveal melanoma源in黑colorelementcells恶typeTransformation,cancanandcongenitaltypecolorelementMalignant transformation of nevichangehaveclose。

Evolution from other eye diseases:long-termUveitis,eyeinternalRecurrentbleeding、eyeinternaldifferentexist留cancanSecondary malignancytypechange。

Age and sex:uveal melanomacommonly occurs in50years and olderadults,male-to-female ratioapproximately1.5:1;retinoblastomamore见in5years and younger。


Common Symptoms

Visiondifferentnormalandvisual field defect: Solitaryeyedecreased visual acuity, Blurred visionorVisual field defectlose,childrencancandue tonomethodAccurately expresswhileappearing频complex揉eye, Squintingeyeor撞proceedas。

leukocoria(Leukocoria):retinoblastomaof典typemanifestation,due totumorBlocking light reflex, pupillary areapresenting白colorReflex, observedin85%ofIn pediatric patients.

proptosisandpositionDisplacement:uveal melanomaetc.tumorgrowthcausingeye球towardanterioroutstandingortowardoneLateral deviation, with conjunctivalcongestionedema。

painand炎conditionreaction:advanced-stagetumornecrosis、bleedingorSecondary glaucomaeyeCausingeyePain,headache, With conjunctivalcongestion, Corneaedema。

eyelidSwellingandunderPtosis:Tumor invadeseyeexternal肌or眶internalstructurecausing。

diplopia:eye肌receive累ornerveinvasioncausing。

systemicsymptoms:minorityadvanced-stagepatientscanappearingbody weightunderdecrease、fatigueetc.。


primarytypeandclassification

retinoblastoma(childrenmostcommon):

minutetype:internallifetype、externallifetype, Mixedcombinegrowthtype, Diffusegrowthtype, Lichenoidgrowthtype

staging:eyeinternalstage, Glaucomaeyestage、eyeexternalExtensionstage、systemicmetastasisstage

uveal melanoma(adultsmostcommon):

according toregionpositionminute: Iris melanomacolorelementtumor, Ciliary bodyconditionbody黑colorelementtumor, Choroidal melanomacolorelementtumor

according tocellsminutetype: Spindleformcellstype(prognosisrelativelygood)、upperEpithelioidcellstype(relatively poor prognosis)

othertype:

eyelidbasal cell carcinoma:mostcommoneyelidmalignant tumor

Conjunctivasquamous cell carcinoma:andHPVinfectionrelated

eyeinternallymphatictumor:moreassystemiclymphatictumor累andeyeregion


Clinical Staging

eyeinternaltumorstillno统onestagingsystem,typicallybased ontumorsize、position、invasionextentperformedstaging:

early-stage:tumorsmall,localizedineyeinternal, Not yetinvasionimportantstructure

mid-stage:tumorrelativelylarge, InvolvingandRetina, opticnerve

advanced-stage:Tumor invadeseyeexternalstructure,or已Distant metastasis present


Diagnosis

fundus examination:disperse瞳posteriordirectly检eye镜orWide-angleeyeFundus photography

Imaging studies:

ocular B-ultrasound:showtumorposition、size、internalregionechoes,retinoblastomamore伴havecalcification

CT/MRI:assessmenttumorextent, Visionnerveinvasion, Cranialinternalmetastasis

fundus fluorescein angiography(FFA):assessmenttumorBlood supply

ultrasound biomicroscopy(UBM):assessment睫conditionbody, Iristumor

optical coherence tomography(OCT):assessmentRetinastructure

pathological biopsy: Necessarytimepunctureorsurgical resectionconfirmed diagnosis


Prevention and Follow-up

geneticConsultation:havefamily historythoseperformedgenetic testing

childrenscreening:havefamily historychildrenfrom出liferiseregularlyperformedfundus examination(every 3-6 months)

紫externalRadiation protection: Outdoorexternal活movetimeWearing UV-protectiveexternal线eyeGlasses,wideBrimmed hat

regularbodyExamination:adults50years and olderannuallyfundus examination

early-stagesymptomsmonitor:childrenappearingStrabismus, photophobiaorPupillary light reflexdifferentnormal立namelythen诊

follow-up:after treatmentbased ontumortypestaging,every1-6monthfollow-up examinationeye底andImaging

Treatment Plan Evaluation Request

EVALUATION OF DIAGNOSIS AND TREATMENT PLAN
Medical Condition