Introdução
O que você precisa saber de cara
Um neoplasma ocular é um tipo raro de tumor do olho. Neoplasmas oculares podem afetar todas as partes do olho e podem ser benignos (não cancerosos) ou malignos (cancerosos), caso em que é conhecido como câncer de olho. Cânceres de olho podem ser primários ou metastáticos. Os dois tipos de câncer mais comuns que se espalham para o olho a partir de outro órgão são o câncer de mama e o câncer de pulmão. Outros locais de origem menos comuns incluem próstata, rim, tireoide, pele, cólon e sangue ou medula óssea.
Escala de raridade
<1/50kMuito rara
1/20kRara
1/10kPouco freq.
1/5kIncomum
1/2k
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Entender a doença
Do básico ao detalhe, leia no seu ritmo
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Sinais e sintomas
O que aparece no corpo e com que frequência cada sintoma acontece
Linha do tempo da pesquisa
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Genética e causas
O que está alterado no DNA e como passa nas famílias
Nenhum gene associado encontrado
Os dados genéticos desta condição ainda estão sendo catalogados.
Diagnóstico
Os sinais que médicos procuram e os exames que confirmam
Tratamento e manejo
Remédios, cuidados de apoio e o que precisa acompanhar
Onde tratar no SUS
Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)
🇧🇷 Atendimento SUS — Osteoma coroide
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Dados de DATASUS/CNES, SBGM, ABNeuro e Ministério da Saúde. Sempre confirme a disponibilidade diretamente com o estabelecimento.
Pesquisa ativa
Ensaios clínicos abertos e novidades científicas recentes
Ensaios em destaque
Pesquisa e ensaios clínicos
1 ensaios clínicos encontrados.
Publicações mais relevantes
Choroidal Osteoma with Focal Choroidal Excavation Masquerading as Active Vogt-Koyanagi-Harada: A Case Report.
Choroidal osteoma is a rare, benign ossifying tumor of the choroid that can present with clinical features overlapping those of inflammatory choroidal lesions. In patients with a history of Vogt-Koyanagi-Harada (VKH) disease, distinguishing between inflammatory relapse and non-inflammatory choroidal pathology can be particularly challenging. This case report highlights the diagnostic pitfalls associated with choroidal osteoma in the setting of prior VKH and underscores the importance of comprehensive multimodal imaging to ensure accurate diagnosis and appropriate management. A 39-year-old female with a 14-year history of VKH disease, who had been stable off immunosuppressive therapy since 2016, presented in early 2024 with a 7-week history of cloudy vision in the right eye. She was initially diagnosed with a recurrent posterior VKH relapse and treated with high-dose intravenous corticosteroids followed by an oral taper, resulting in symptomatic improvement. However, further multimodal imaging - including wide-field fundus photography, optical coherence tomography (OCT), fundus autofluorescence, OCT angiography, fluorescein angiography, enhanced depth imaging OCT (EDI-OCT), and B-scan ultrasonography - revealed a yellow-orange, minimally elevated subretinal lesion associated with focal choroidal excavation. These findings were consistent with choroidal osteoma and confirmed by EDI-OCT and B-scan ultrasonography. This case illustrates a rare instance of choroidal osteoma masquerading as a posterior relapse of VKH disease. It emphasizes the critical importance of differentiating inflammatory from non-inflammatory choroidal lesions in patients with a history of uveitis. Careful interpretation of multimodal imaging is essential to avoid misdiagnosis, prevent unnecessary immunosuppressive treatment, and reduce associated risks, ultimately leading to improved patient outcomes.
Novel Clinical Observations after Photodynamic Therapy in Choroidal Osteoma: A Three-Case Series.
Choroidal osteoma is a benign intraocular tumor that often presents in the juxtapapillary or macular region of young adult females. Factors contributing to severe vision impairment include tumor growth to the fovea, isolated subretinal fluid (SRF), alterations of the retinal pigment epithelium, macular edema, or serosanguineous SRF related to the development of choroidal neovascularization. This paper evaluates the effectiveness of photodynamic therapy (PDT) in treating symptomatic SRF and preventing foveal involvement, providing valuable long-term data and highlighting some previously unreported minor complications related to the treatment. In case 1, a 23-year-old woman with a juxtapapillary choroidal osteoma and symptomatic SRF was treated with PDT. Two months later, the visual acuity improved from 20/50 to 20/20 with complete resolution of the fluid. In case 2, an asymptomatic 22-year-old woman with a juxtapapillary choroidal osteoma was treated with a single PDT session, and progressive tumor decalcification was observed. Visual field testing after the treatment revealed the development of two small deep scotomas inferior to the physiological blind spot, which were not perceived by the patient, while visual acuity has remained at 20/20 15 years after the treatment. In case 3, a 38-year-old woman with a paracentral scotoma related to a juxtafoveal choroidal osteoma was treated with a single PDT session to prevent potential complications. Twenty days after the treatment, a subretinal hemorrhage was observed between the posterior margin of the tumor and the fovea, and 2 months later it spontaneously disappeared. Tumor decalcification was noticed 4 months after the treatment, the visual acuity dropped to 20/30, and the paracentral scotoma increased. Since then, the functional parameters have remained stable. This study reinforces the established role of PDT in the management of choroidal osteoma, resolving SRF, promoting tumor decalcification and preventing central tumor extension after long-term follow-up. However, it also highlights the occurrence of a self-limited subretinal hemorrhage following the application of PDT and the development of permanent paracentral scotomas as a treatment-related effect.
[Neovascular complications of choroidal osteoma: Diagnosis and treatment].
Choroidal osteoma is a rare benign ocular tumor, with neovascular complications being even less common. The diagnosis is greatly facilitated by multimodal imaging techniques. However, treatment remains a challenge, as no standardized protocols exist, and current approaches rely primarily on intravitreal injections of anti-VEGF agents. We describe the case of a 45-year-old patient with no significant medical history who presented in 2020 with a progressive macular syndrome, characterized by decreased visual acuity and a central scotoma over several months. Ophthalmologic examination of the right eye was unremarkable, while the left eye showed reduced visual acuity of 3/10. The anterior segment was normal with a clear lens. Fundoscopy revealed a well-demarcated yellowish juxta-papillary subretinal lesion extending into the papillomacular area. Optical coherence tomography (OCT) demonstrated serous retinal detachment, intraretinal macular edema, and retinal pigment epithelial (RPE) detachments, along with a juxta-papillary eovascular membrane. A-scan ultrasonography confirmed the diagnosis of choroidal osteoma, showing a hyper-echogenic lesion with posterior shadowing. Retinal angiography and indocyanine green angiography (ICG) revealed occult neovascularization extending into the papillomacular area. The patient was treated with intravitreal anti-VEGF injections. Although the therapeutic response was gradual, injections every six weeks successfully maintained visual acuity at 7/10 and resolved the intra- and subretinal fluid. The management of neovascular complications in choroidal osteoma remains complex due to the absence of standardized treatment protocols. Anti-VEGF therapy shows promise, albeit with a slow response, and requires sustained long-term administration to optimize visual outcomes and preserve visual function.
Optical coherence tomography and fundus autofluorescence features in choroidal and retinal tumors.
The aim of the study was todescribe the clinical features, optical coherence tomography (OCT) and fundus autofluorescence (FAF) imaging in patients with choroidal and retinal tumors. Ninety eyes of 89 patients with treatment-naive macular, midperipheral, and juxtapapillary choroidal and retinal tumors were retrospectively included in the study. All patients underwent a complete ophthalmic examination, B-mode ultrasonography, OCT, and FAF imaging. OCT and FAF images taken at the time of diagnosis were reviewed retrospectively. Choroidal nevus (CN), choroidal malignant melanoma (CMM), optic disc melanocytoma (ODM), circumscribed choroidal hemangioma (CCH), and choroidal osteoma (CO) displayed dome-shaped contour on OCT, while choroidal metastases (CM) showed a lumpy bumpy contour. CN had preserved choriocapillaris. Choroidal compression was observed in all choroidal tumors except CCH which showed vascular expansion. CMM was the most common lesion displaying overlying lipofuscin. Intraretinal fluid was seen mostly in CCM and CCH. Subretinal fluid (SRF) was usually observed in CM, CMM, and CCH. Drusen and pigment epithelial detachment (PED) were noted in CN. While the pattern of hyperautofluorescence (hyper-AF) was most marked in CMM, other tumors including CCH and CM occasionally showed similar FAF appearance. Comparing CN and CMM; CN displayed more drusen and PED (p = 0.024 and p = 0.037 respectively) and CMM showed more SRF, intraretinal fluid, and shaggy photoreceptor (p = 0.040, p < 0.001, and p < 0.001 respectively). CN displayed more hypo-AF and iso-AF (p < 0.001) while CMM showed significantly more diffuse and patchy hyper-AF (p < 0.001). Characteristic findings in OCT and FAF guide clinicians in the differential diagnosis of choroidal and retinal tumors and allow for earlier detection and improved treatment outcomes.
Choroidal Osteoma Complicated by Choroidal Neovascularization: A Case Report.
A 13-year-old girl with no prior systemic or ocular comorbidities presented to the eye clinic at Shifa International Hospital, Islamabad, Pakistan, with complaints of blurred vision in her left eye. Fundus examination revealed a well-defined, yellow-orange lesion at the posterior pole. B-scan ultrasonography demonstrated an echo-dense lesion, most prominent at low gain, while swept source optical coherence tomography (SS-OCT) showed a hyperreflective choroidal mass with associated subretinal fluid (SRF). Based on these findings, a diagnosis of choroidal osteoma complicated by choroidal neovascularization (CNV) was established. This case report describes the management of a pediatric case of CNV related to choroidal osteoma with a series of intravitreal anti-vascular endothelial growth factor (anti-VEGF) injections over nine months, resulting in significant regression of CNV and a reduction in SRF. She continues to be monitored with multimodal imaging and intermittent therapy, demonstrating favorable anatomical and functional outcomes.
Publicações recentes
Unilateral Retinal Pigment Epithelium Dysgenesis (URPED) - The Expanded Spectrum and New Insights from Multimodal Imaging.
Photocoagulation-induced Large Posterior Staphyloma in Choroidal Osteoma.
Choroidal Osteoma with Focal Choroidal Excavation Masquerading as Active Vogt-Koyanagi-Harada: A Case Report.
Novel Clinical Observations after Photodynamic Therapy in Choroidal Osteoma: A Three-Case Series.
[Neovascular complications of choroidal osteoma: Diagnosis and treatment].
📚 EuropePMC244 artigos no totalmostrando 148
Choroidal Osteoma with Focal Choroidal Excavation Masquerading as Active Vogt-Koyanagi-Harada: A Case Report.
Case reports in ophthalmologyNovel Clinical Observations after Photodynamic Therapy in Choroidal Osteoma: A Three-Case Series.
Ocular oncology and pathology[Neovascular complications of choroidal osteoma: Diagnosis and treatment].
Journal francais d'ophtalmologieChoroidal Osteoma Complicated by Choroidal Neovascularization: A Case Report.
CureusAnti-vascular endothelial growth factor therapies in ophthalmology.
Medical hypothesis, discovery & innovation ophthalmology journalSecondary Choroidal Osteoma in the Setting of Uveal Pathology: 4 Case Reports and Review.
Ocular oncology and pathologyAntivascular Endothelial Growth Factors for the Management of Choroidal Neovascularization Associated with Choroidal Osteoma: A Case Study-Based Review.
Journal of current ophthalmologyDe novo pediatric choroidal Osteoma: A longitudinal observation since inception and through treatment.
American journal of ophthalmology case reportsPrevalence and clinical correlates of focal choroidal excavation in a large cohort of Chinese patients with choroidal osteoma.
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Ophthalmology. RetinaGrowing choroidal osteoma: Treated by proton beam radiation.
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Photodiagnosis and photodynamic therapyAngioid Streaks and Choroidal Osteoma in Pseudoxanthoma Elasticum.
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American journal of ophthalmology case reportsOptical coherence tomography and fundus autofluorescence features in choroidal and retinal tumors.
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Retinal cases & brief reportsDifferential diagnosis of myopic choroidal neovascularization (mCNV): insights from multimodal imaging and treatment implications.
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The Pan African medical journalLong term results of photodynamic therapy in intraocular tumors.
Photodiagnosis and photodynamic therapyDe novo choroidal osteoma after laser photocoagulation of a peripapillary choroidal neovascular membrane.
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Korean journal of ophthalmology : KJORapid enlargement of choroidal osteoma in an adult patient.
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Case reports in ophthalmologyBilateral Choroidal Osteoma in a Teenage Girl With Chronic Posterior Scleritis.
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Current eye researchCase Report: Multimodal Imaging in a Rare Case of Morning Glory Disc Anomaly Complicated With Choroidal Ossification.
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GMS ophthalmology casesAppearance of Tumor Vessels in Patients With Choroidal Osteoma Using Swept-Source Optical Coherence Tomographic Angiography.
Frontiers in oncologyComplications, treatments, and visual prognosis of choroidal osteomas.
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Retina (Philadelphia, Pa.)Spontaneous Regression of Asymptomatic Bilateral Choroidal Osteoma with Preserved Vision.
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Journal francais d'ophtalmologieNovel OCT findings in choroidal osteoma: brief report.
International journal of retina and vitreousIntravitreally injected ranibizumab versus photodynamic therapy for CNV secondary to choroidal osteoma: a 7-year follow-up case report.
International journal of ophthalmologySecondary choroidal neovascularization due to choroidal osteoma after 9 years follow-up.
BMC ophthalmologyChoroidal osteoma associated with focal choroidal excavation.
Journal francais d'ophtalmologiePhotodynamic therapy for macular choroidal osteoma.
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Journal of ophthalmic & vision researchRecurrent posterior scleritis with secondary choroidal osteoma in a child.
Indian journal of ophthalmologyThe Role of Optical Coherence Tomography Angiography in Ranibizumab-Treated Choroidal Neovascularization in Choroidal Osteoma.
Case reports in ophthalmologyFocal Choroidal Excavation in a Case of Choroidal Osteoma Associated with Choroidal Neovascularization.
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MedicineSmall Symptomatic Unilateral Choroidal Osteoma Diagnosed with Enhanced-Depth Imaging Optical Coherence Tomography and Thin-Slice Computed Tomography: 2 Clinical Cases.
Case reports in ophthalmologyNovel observations in choroidal osteoma by multispectral imaging: a pilot case series.
International ophthalmology[Choroidal calcification associated to chondrocalcinosis].
Revista medica del Instituto Mexicano del Seguro SocialBilateral choroidal osteoma with unilateral polypoidal choroidal vasculopathy treated with conbercept.
International journal of ophthalmologyContribution of swept-source OCT-angiography in analysis of choroidal osteoma and its quiescent neovascular complications: A case study.
American journal of ophthalmology case reportsDARK WITHOUT PRESSURE IN A CASE OF CHOROIDAL OSTEOMA.
Retinal cases & brief reportsIn vivo optical biopsy of choroidal osteoma: a swept source optical coherence tomography-based tumor characterization.
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European journal of ophthalmologyPolypoidal choroidal vasculopathy as a complication of choroidal osteoma: A case report.
MedicineChoroidal osteoma: the varied response of subretinal fluid to anti-VEGF agents.
BMJ case reportsSpontaneous resolution of serous retinal detachment caused by choroidal mass after a first trimester abortion.
Yeungnam University journal of medicineBilateral Choroidal Osteomas With Choroidal Neovascularization.
JAMA ophthalmologyFocal choroidal excavation and pitchfork sign in choroidal neovascularisation associated with choroidal osteoma.
European journal of ophthalmologySequential imaging of a case of choroidal osteoma using swept-source OCT and optical coherence tomography angiography: A 4-year follow-up study.
Indian journal of ophthalmologyDoughnut osteoma: A rare case of circumpapillary choroidal osteoma.
Indian journal of ophthalmologyBilateral Choroidal Osteoma of Childhood.
JAMA ophthalmologyMultiple choroidal osteomas in a boy - a rare presentation: a case report.
Journal of medical case reportsMultimodal Imaging in Bilateral Nature of the Choroidal Osteoma After Intraocular Inflammation Caused by Harada Disease.
Retina (Philadelphia, Pa.)Bilateral Choroidal Osteoma Complicated by Bilateral Choroidal Neovascularization.
Ophthalmic surgery, lasers & imaging retinaOCT Angiography: Imaging of Choroidal and Retinal Tumors.
Ophthalmology. RetinaBilateral pale posterior pole sans pain: A "hard" sell.
Indian journal of ophthalmologyFUNDUS AUTOFLUORESCENCE PREDICTING GROWTH OF A CHOROIDAL OSTEOMA IN A 13-YEAR-OLD GIRL.
Retinal cases & brief reportsPHOTODYNAMIC THERAPY FOR EXTRAFOVEOLAR CHOROIDAL OSTEOMA.
Retina (Philadelphia, Pa.)Bilateral choroidal osteoma associated with langerhans cell histiocytosis, a coincidence?
Journal of current ophthalmologyOPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY FINDINGS IN A CASE OF CHOROIDAL NEOVASCULARIZATION SECONDARY TO UNILATERAL RETINAL PIGMENT EPITHELIUM DYSGENESIS TREATED WITH INTRAVITREAL BEVACIZUMAB THERAPY.
Retinal cases & brief reportsIn vivo diagnosis of intraocular osseous metaplasia in neovascular age-related macular degeneration.
Indian journal of ophthalmologyMulticolor imaging in choroidal osteomas.
International journal of retina and vitreousChoroidal Osteoma Accompanied by Proliferative Diabetic Retinopathy.
Korean journal of ophthalmology : KJOA case of choroidal osteoma in a 17-year-old female.
Oman journal of ophthalmology[Serous retinal detachment secondary to choroidal osteoma].
Journal francais d'ophtalmologie[Atypical choroidal osteoma: Case report].
Journal francais d'ophtalmologieMultimodal imaging in choroidal osteoma.
International journal of retina and vitreousChoroidal neovascularization due to choroidal osteoma treated with anti-vascular endothelial growth factor therapy: An optical coherence tomography angiography study.
European journal of ophthalmologyBone inside eye: choroidal osteoma presenting as exudative retinal detachment: a challenge to diagnosis.
BMJ case reportsChoroidal osteoma in a preterm infant.
Indian journal of ophthalmology[Pai syndrome: Two new cases with unusual manifestations].
Archivos argentinos de pediatriaCorrigendum to 'Intravitreal ranibizumab for treatment of choroidal neovascularization secondary to a bilateral choroidal osteoma' [Am. J. Ophthalmol. Case Reports (4) (2016) 7-10].
American journal of ophthalmology case reportsChoroidal osteoma with choroidal excavation and associated neovascular membrane: An OCT-angiography study.
Archivos de la Sociedad Espanola de OftalmologiaImaging of Neovascular Membrane Over a Choroidal Osteoma by OCT Angiography.
OphthalmologyFour-year SD-OCT follow-up of a treated bilateral choroidal osteoma complicated by choroidal neovascularisation.
Journal francais d'ophtalmologieOCT Angiography Characteristics of Choroidal Osteoma.
Ophthalmology. RetinaChoroidal osteoma and pattern dystrophy of retinal pigment epithelium.
International ophthalmologyNonconforming Deep Focal Choroidal Excavation in a Patient With Choroidal Osteoma: A Diagnostic Dilemma.
Ophthalmic surgery, lasers & imaging retina[Choroidal Osteoma in a Male Patient - Multimodal Imaging].
Klinische Monatsblatter fur AugenheilkundeA Case of Rare Choroidal Tumor, Choroidal Osteoma.
Kathmandu University medical journal (KUMJ)Choroidal Osteoma and Secondary Choroidal Neovascularization Treated with Ranibizumab.
Turkish journal of ophthalmologyChoroidal excavation in choroidal osteoma complicated by choroidal neovascularization.
Eye (London, England)Successful management of choroidal neovascular membrane secondary to choroidal osteoma with intravitreal bevacizumab.
Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society[Newly occurring loss of visual acuity in choroidal osteoma].
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen GesellschaftLater Development of Posterior Staphyloma in Choroidal Osteoma With Choroidal Neovascularization.
Retina (Philadelphia, Pa.)The Histopathological Finding of the Surgically Extracted Atypical Dome-Shaped Choroidal Osteoma.
Case reports in ophthalmological medicineAssessment of choroidal osteoma complicating choroidal neovascularization by optical coherence tomography angiography.
International ophthalmology[Uncomplicated choroidal osteoma].
Journal francais d'ophtalmologieEvaluation of choroidal tumors with optical coherence tomography: enhanced depth imaging and OCT-angiography features.
Eye (London, England)Intravitreal ziv-aflibercept for the treatment of choroidal neovascularisation associated with conditions other than age-related macular degeneration.
The British journal of ophthalmology[Bilateral choroidal osteoma].
Journal francais d'ophtalmologieMULTIMODAL FUNDUS IMAGING OF OUTER RETINAL TUBULATIONS IN CHOROIDAL OSTEOMA PATIENTS.
Retina (Philadelphia, Pa.)Choroidal Osteoma Deossification Visualized by Enhanced Depth Imaging Spectral-Domain Optical Coherence Tomography.
Ophthalmic surgery, lasers & imaging retina[Choroidal neovascularisation in a patient with choroidal osteoma visualized by OCT angiography].
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen GesellschaftEnhanced depth imaging optical coherence tomography of choroidal osteoma with secondary neovascular membranes: report of two cases.
Arquivos brasileiros de oftalmologiaEtiology and treatment of choroidal neovascularization in pediatric patients.
European journal of ophthalmologyIntravitreal ranibizumab for treatment of choroidal neovascularization secondary to a bilateral choroidal osteoma.
American journal of ophthalmology case reportsOCT angiography in choroidal neovascularization secondary to choroidal osteoma.
Acta ophthalmologicaSwept source: optical coherence tomography angiography features of choroidal osteoma with choroidal neovascular membrane.
BMJ case reportsIntravitreal Bevacizumab for Management of Choroidal Osteoma without Choroidal Neovascularization.
Journal of ophthalmic & vision researchIntravitreal bevacizumab monotherapy for choroidal neovascularisation secondary to choroidal osteoma.
Eye (London, England)Anti-vascular endothelial growth factors for choroidal neovascularization secondary to choroidal osteoma: Long-term results.
Oman journal of ophthalmologyBilateral Multifocal Choroidal Osteoma with Choroidal Neovascularization.
Case reports in ophthalmological medicineOptical Coherence Tomography Angiography for Detecting Choroidal Neovascularization Secondary to Choroidal Osteoma.
Ophthalmic surgery, lasers & imaging retina[Imaging choroidal osteoma with the Deep Range Imaging Optical Coherence Tomography – a case report].
Klinika ocznaChoroidal osteoma: Bone in the eye.
Joint bone spineA case of choroidal osteoma in a 10-year-old child.
International medical case reports journalIdiopathic polypoidal choroidal vasculopathy masquerading as choroidal tumors: one year follow-up of a peripheral lesion.
Arquivos brasileiros de oftalmologiaAnatomical and visual outcomes of ranibizumab injections in retinal pigment epithelium tears.
Arquivos brasileiros de oftalmologiaReal-time in vivo micromorphology and histopathology of choroidal osteoma using enhanced depth imaging.
Indian journal of ophthalmologyDiagnostic and Therapeutic Challenges.
Retina (Philadelphia, Pa.)[Manifestation of bilateral choroidal osteoma in childhood. Progressive myopia due to staphyloma posticum].
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen GesellschaftKeratoglobus: An experience at a tertiary eye care center in India.
Indian journal of ophthalmologyA Second New Choroidal Osteoma in the Same Eye: Differences between Them with New Imaging Techniques.
Case reports in ophthalmological medicineReview of spectral domain enhanced depth imaging optical coherence tomography of tumors of the choroid.
Indian journal of ophthalmologyBilateral choroidal osteoma: visual acuity at 45-year follow-up.
Retinal cases & brief reportsLong-term outcomes of intravitreal injection of bevacizumab for choroidal neovascularization associated with choroidal osteoma.
Clinical ophthalmology (Auckland, N.Z.)Enhanced depth imaging-optical coherence tomography of choroidal osteoma.
JAMA ophthalmologyRescue therapy with intravitreal aflibercept for choroidal neovascularization secondary to choroidal osteoma non-responder to intravitreal bevacizumab and ranibizumab.
International ophthalmologySclerochoroidal calcification: clinical features, outcomes, and relationship with hypercalcemia and parathyroid adenoma in 179 eyes.
Retina (Philadelphia, Pa.)Associações
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Referências e fontes
Bases de dados externas citadas neste artigo
Publicações científicas
Artigos indexados no PubMed ligados a esta doença no grafo RarasNet — título, periódico e PMID direto da fonte, sem intermediação de IA.
- Choroidal Osteoma with Focal Choroidal Excavation Masquerading as Active Vogt-Koyanagi-Harada: A Case Report.
- Novel Clinical Observations after Photodynamic Therapy in Choroidal Osteoma: A Three-Case Series.
- [Neovascular complications of choroidal osteoma: Diagnosis and treatment].
- Optical coherence tomography and fundus autofluorescence features in choroidal and retinal tumors.
- Choroidal Osteoma Complicated by Choroidal Neovascularization: A Case Report.
- Unilateral Retinal Pigment Epithelium Dysgenesis (URPED) - The Expanded Spectrum and New Insights from Multimodal Imaging.
- Photocoagulation-induced Large Posterior Staphyloma in Choroidal Osteoma.
Bases de dados e fontes oficiais
Identificadores e referências canônicas usadas para montar este verbete.
- ORPHA:674965(Orphanet)
- MONDO:0971130(MONDO)
- Busca completa no PubMed(PubMed)
Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.
Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar
