It is characterized by a yellowish, well demarcated lesion in the juxtapapillary or macular area. Open access full text article choroidal osteoma with. We present a case of choroidal osteoma with choroidal neovascularization as a complication. Choroidal osteoma is a benign calcified tumor that can focally replace normal vascular tissue with mature bone. Calcifications in the eye may be present in the choroid and retinal pigment epithelium rpe and may be secondary to trauma, chronic inflammation and infection, hypercalcemia or hyperparathyroidism. Osteomas definition of osteomas by medical dictionary. Aug 08, 2019 initial treatment of osteoid osteoma is nonoperative.
Solitary osteoma cutis is by far the most common form, and typically occurs as a reactive process in association with other inflammatory or neoplastic conditions. This free online tool allows to combine multiple pdf or image files into a single pdf document. A peripheral osteoma arises from the periosteum, a central osteoma from the endosteum, and an extraskeletal osteoma in the soft tissue 14. It is generally unilateral, seen in young females, mostly in the juxtapapillary and macular region appearing as irregular slightly elevated, deep orangeyellow choroidal mass with welldefined scalloped borders. Osteoid osteoma is a benign skeletal neoplasm composed of osteoid and woven bone that rarely exceeds 1. She reports that she recently failed a school screening. The diagnosis of choroidal osteoma is mainly clinical. Rescue therapy with intravitreal aflibercept for choroidal.
Choroidal osteoma usually occurs in 2030 year old, healthy, white women as a welldefined, unilateral 75%, solitary, yellow orange, slowgrowing juxtapapillary lesion. Osteoid osteoma mri mri has not been useful in the diagnosis of osteoid osteoma. Though present from birth, it is usually diagnosed during the second or third. Retinal astrocytic hamartoma versus choroidal osteoma. Discussion choroidal osteomas are benign juxtapapillary choroidal ossified tumors.
Described herein is the case of a 16year old female presenting with a peripapillary lesion diagnosed as choroidal osteoma on multimodal imaging. Co is often located in the juxtapapillary or macular region and is unilateral in the majority of cases2. Spectral domainoptical coherence tomography analysis of. The diagnostic imaging appearances of three choroidal osteomas osseous choristomas are presented. Color photograph of a choroidal osteoma with associated choroidal neovascularization. Soda pdf merge tool allows you to combine two or more documents into a single pdf file for free. This treatment option is low in both risk and morbidity and is therefore the best option in lesions that are difficult to access surgically because of the risks. There are no reports of osteoma malignant transformation 1,6,17. Co is typically unilateral 80% of cases and it usually affects young healthy female patients. In our case, the clinical feature of the tumor was atypical for all differential diagnoses, including choroidal osteoma and amelanotic malignant melanoma, so it was extremely challenging to make a clinical diagnosis as choroidal osteoma using conventional noninvasive examinations. Osteoma cutis may manifest as a solitary firm papule, multiple papules, or even plaques. Osteomas may be detected with routine radiographic examination or the tumors may enlarge and cause symptoms. In the largest case series on choroidal osteoma including 74 eyes of 61 patients followed up for a period of 26 years, carol and colleagues demonstrated that choroidal osteoma is a disease of young females. A healthy 20yearold female presented to the oculoplastics clinic with a 9month history of left upper lid droopiness.
Multiple choroidal osteomas in a boy a rare presentation. The proximal femur is the most common site of occurrence. Optical coherence tomography of retinal and choroidal tumors. Dec 27, 20 osteoid osteoma bone scan a bone scan is helpful in detecting the doubledensity sign, which is a focal area of increased activity with a second smaller area of increased uptake superimposed on it, is said to be diagnostic of osteoid osteoma. Between 8 and 30 percent of cases remain asymptomatic. Diagnosis and monitoring of choroidal osteoma through. Its recurrence is rare 8,18, with only one case described in the literature 19.
Aug 08, 2019 osteoid osteoma is a benign osteoblastic tumor that was first described in 1930 by bergstrand. Some publications report a benefit with intravitreal bevacizumab 9. Over time, colour changes from yellow orange to yellowwhite. A 16yearold caucasian female with a 6month history of decreased visual acuity and metamorphopsia in the left eye is reported. Choroidal osteoma is a rare tumor which features intraocular bone formation. Epidemiology choroidal osteomas are typically found in young caucasian women 1. The neovascularization is located on the papillomacular bundle, and small spots of subretinal hemorrhage are noticed around it. Choroidal osteoma related vision loss is not usually treatable. Osteoid osteoma19 yr old male withpain in in the dorsalaspect of the medial aspect of left mid foot. This tumor can be complicated by choroidal neovascularization which is a cause of impaired vision in this condition. Pdf merge combinejoin pdf files online for free soda pdf. Osteoid osteomas can affect people of all ages but they occur more frequently in children and young adults.
Choroidal osteoma is a rare, benign, ossifying tumour of the choroid of unknown aetiology. Choroidal osteoma rare benign tumour of the choroid, typically occurring unilaterally in the juxtapapillary or macular areas. Jaffe described it in 1935 and was the first to recognize it as a unique entity. Originally intended primarily for retina specialists to image the macula, it has found its role in other subspecialties that include glaucoma, cornea, and ocular oncology. Choroidal osteoma choroidal osteoma fluorescein angiography demonstrates subretinal neovascularization at the macular margin. Osteomas most frequently occur in the frontal and ethmoid sinuses, and are rare in the maxillary sinus.
Choroidal osteoma definition of choroidal osteoma by. Aug 27, 2008 osteoid osteoma is a benign tumor of the growing skeleton. Choroidal osteoma co is a rare benign tumor of the choroid, which is composed of mature bone trabecular andor compact and vascular channels 1,2,3,4. Enhanced depth imaging optical coherence tomography of. Choroidal osteoma is a rare osseous benign tumour typically occurring in otherwise healthy young women. Routine fundus photography 18 months before presentation demonstrated a normal retina and choroid without evidence of the lesion. The fundus of the left eye revealed a well defined lesion in the macula region. A second case was presented in 1975 in the verhoeff society by van dyk and published in 1978 by williams, font, van dyk, and riekhof williams et al. Unilateral choroidal osteoma with evidence of choroidal. New tests that were unavailable during the first diagnosis were performed such as fundus autofluorescence or enhanced depth imagingoptical coherence tomography edioct.
Osteoid osteoma is a benign tumor of the skeletal system which primarily targets younger individuals, and most commonly develops in long bones. The most common complication of co is choroidal neovascularization cnv, an important cause of. Although choroidal osteoma is benign, it usually results in poor vision over time. Mar 24, 2011 we present a case report highlighting the unusual location and atypical imaging characteristics of an osteoid osteoma in the juxtaarticular region of the femoral head, and treatment of the condition with radiofrequency ablation. On occasion, a choroidal osteoma may be associated with subretinal neovascularization abnormal blood vessels beneath the retina, which are typically treated with laser. Choroidal osteomas are rare benign ossifying tumors that appear as irregular slightly elevated, yellowwhite, juxtapapillary, choroidal mass with welldefined geographic borders, depigmentation of the overlying pigment epithelium. Choroidal osteoma with neovascular membrane managed with. Examinations indicate that pcv could be more like a neovasculopathy occurring in a variety of different diagnoses other than a distinct abnormality of the inner choroidal vasculature 2.
It is characterized by proliferation of either compact or cancellous bone in an endosteal or periosteal location. An amelanotic choroidal nevus can be relatively flat like a choroidal osteoma but a nevus differs in that it has less distinct margins and can have drusen on. In the posterior pole, a flat choroidal lesion, with very high reflectivity and shadowing of the posterior orbital contents, was observed in both eyes. It may be classified as peripheral, central, or extraskeletal. Backgroundaims to assess spectral domainoptical coherence tomography sdoct contribution to choroidal osteoma characterisation.
If you are looking for a way to combine two or more pdfs into a single file, try pdfchef for free. Choroidal osteoma choroidal osseous choristoma is a benign tumor of unknown etiology first described by gass et al 1978. After 10 years the patient presented a second choroidal osteoma in the same eye. The osteoma cutis may persist long after the inflammatory condition has resolved. They may be complicated by choroidal neovascularization cnv which may lead to loss of vision, and in such cases photocoagulation therapy may be of benefit, although overall response is poor 3. Diagnosis of choroidal osteoma was established using spectral domain optical coherence tomography oct, fundus fluorescein angiography ffa, indocyanine green angiography icg, and b. An osteoid osteoma is a benign noncancerous bone tumor that usually develops in the long bones of the body such as the thighbone and shinbone. Systemically, there were no other findings of familial adenomatous polyposis gardner syndrome. Choroidal excavation in choroidal osteoma complicated by.
Oct 22, 2011 paranasal sinus osteomas are rare benign tumors. This simple webbased tool lets you merge pdf files in batches. Objective to provide longterm followup information on a large series of patients with choroidal osteoma. Choroidal osteoma is an ossified tumor first described in 1978 by gass and associates.
Osteoma in a child choroidal osteoma is a rare intraocular bony tumor that typically manifests as a yellowwhite, welldemarcated mass with geographic pseudopodal margins. Retina today enlargement of choroidal osteoma in a child. Intravitreal ranibizumab in a patient with choroidal. Choroidal osteoma is a rare benign ossifying disorder of the choroid. Pdf enhanced depth imaging optical coherence tomography. Osteoma typically occurs in bones formed by membranous ossification, such as calvarial, facial, and jawbones, with a predilection for the paranasal sinuses. Enhanced depth imaging optical coherence tomography revealed a. Osteoma is a benign tumor composed of compact mature bone arising on the surface of the bone. The authors introduce a 42yearold woman with a choroidal osteoma. Figure 2 from choroidal osteoma osseous choristoma. Although the ophthalmoscopic and topographic appearance of sclerochoroidal calcification is characteristic, it is often unrecognized or misdiagnosed. Department of ophthalmology, north texas retina consultants, usa. Osteoid osteoma is a relatively common benign bone tumor.
Choroidal osteoma choroidal osteoma with scalloped edges, pigment on surface and yellow coloration. Visual acuity of the right eye was decreased to 20200 from macular rpe loss and choroidal neovascularization scarring. Clinical presentation involves intense localized pain, which is often not relieved by analgesics. Deze gratis online tool maakt het mogelijk om meerdere pdf bestanden of afbeeldingen te combineren in een pdf document. When developing in the medullary cavity, it is known as enostosis. It presents with pain, which is usually worse at night. Amelanotic choroidal melanoma differs from choroidal osteoma in that it has a yellowbrown color, more elevation and a less welldefined margin. It has thin, delicate trabeculae that enclose large medullary spaces like those in cancellous bone. Choroidal osteoma article about choroidal osteoma by the.
Choroidal osteoma american academy of ophthalmology. Combine pdfs in the order you want with the easiest pdf merger available. A longterm followup of choroidal osteoma intraocular. Choroidal osteoma was first reported by gass et al. In the largest case series on choroidal osteoma including 74 eyes of 61 patients followed up for a period of 26years, carol and colleagues demonstrated that choroidal osteoma is a disease of young females 2. A read is counted each time someone views a publication summary such as the title, abstract, and list of authors, clicks on a figure, or views or downloads the fulltext. The lesion is most commonly located in the cortex of long bones where it is associated with dense, fusiform, reactive sclerosis. An osteoma is a benign osteogenic tumor characterized by compact or cancellous bone proliferation. Our pdf merger allows you to quickly combine multiple pdf files into one single pdf document, in just a few clicks. Choroidal osteomas are rare benign calcific masses of the globe. Typically, affected patients are young and otherwise healthy women 2. The radiographic features consist of a central oval or round nidus surrounded first by a radiolucent area followed by another area of sclerotic bone. The role of ct in the evaluation of choroidal osteoma and the distinctiveness of the ct findings are stressed.
Although various theories such as trauma and infection have been proposed, it is difficult to establish the pathogenesis of osteoma. Osteoma treatment is based on complete surgical removal, on the base, where the bone cortical is located. Choroidal osteoma co is a rare benign ossifying tumor with mature bone replacing choroid and presenting as a yelloworange lesion on fundus examination. Osteoma is a benign often asymptomatic neoplasm, consisting of welldifferentiated matured bone. Optical coherence tomography oct has revolutionized the field of ophthalmology since its introduction 20 years ago. Choroidal osteoma often occurs as a unilateral condition in young females and supposedly associated with congenital causes, inflammatory conditions, and endocrine disorders. Osteoid osteoma of the femoral head treated by radiofrequency. While ophthalmoscopy and fluorescein angiography reveal suggestive ophthalmic findings, echography, plain radiography, and especially computed tomography ct are important in establishing the correct diagnosis. The term choroidal osteoma was coined by gass in 1978 9. Ciliary body melanoma ciliary body melanoma behind the iris as seen through a dilated pupil. Co is typically unilateral 80% of cases and it usually affects young healthy female. Patients usually present with symptoms of blurred vision, metamorphopsia, photophobia or visual field defects. Our patient exhibited the characteristic findings of choroidal osteoma. In ocular oncology, oct provides axial resolution to approximately 7 microns with crosssectional images.
Diagnosis can be made by imaging studies such as ct scanning, and permanent effective treatment can be achieved through percutaneous surgical techniques. A 45yearold male with corelated cnv in his left eye received prior two intravitreal 1. Case report with clinical and angiographic correlation. Since no cnv activity was identified in this case, we suggested periodic clinical followup. However, some males, 10,16,35,37,46,52 young children, 21,23,24,34,38,40 and adults over age 30 years 12,15,21,32,46,50 have been diagnosed with choroidal osteoma. The diagnosis is clinical and can be confirmed with the use of fluorescein or indocyanine angiography, optical coherence tomography, computed tomography. Irregular shape, slightly elevated and typically display a fine superficial vascular network. Department of ophthalmology, shimane medical university, izumo. Ultrasonography shows both hemangioma and osteoma as dense lesions, but osteoma is hyperreflective and casts a shadow. Acknowledgment the authors would like to thank dr vandana dwivedi for her ideas, editing, and completing this paper.
To investigate the effect of aflibercept in a rare case of choroidal neovascularization cnv secondary to choroidal osteoma co and refractory to ranibizumab and bevacizumab. Choroidal osteoma is a benign ossifying tumor characterized by mature bone replacing choroid. Choroidal osteoma co is a benign and rare tumor that is composed of mature bone cells and is more prevalent in females1. Choroidal osteoma is unilateral in approximately 75% of reported cases. Choroidal osteomas are benign, juxtapapillary, choroidal tumors that mandate no treatment. Choroidal osteoma is a choristomatous lesion postulated to be congenital in nature. In bilateral cases, the tumors can appear relatively symmetric or can be asymmetric, in different stages of development, growth, or decalcification. Surgical intervention is generally indicated for patients whose pain is unresponsive to medical therapy, those who cannot tolerate prolonged use of nonsteroidal antiinflammatory drugs nsaids, and those who are not amenable to activity restrictions. After 45 years of followup, choroidal osteoma showed slight enlargement in each eye and choroidal neovascularization and retinal pigment epithelium rpe changes had developed in the right eye. Crawford cm, igboeli oc 2017 unilateral choroidal osteoma with evidence of choroidal neovascularization based on ocular coherence. Split pdf files into individual pages, delete or rotate pages, easily merge pdf files together or edit and modify pdf files.
Acquired choroidal osteoma latin american journal of. Below we show how to combine multiple pdf files into a single document. The authors present enhanced depth imaging optical coherence tomography edi oct and fundus autofluorescence faf characteristics of a patient with bilateral choroidal osteoma and try to make a correlation between two imaging techniques. Choroidal osteoma with neovascular membrane managed with aflibercept and yellow laser raphael pereira da silva, leonardo dias alencar, carlos augusto moreria junior and carlos moreiraneto department of retina and vitreous, eye hospital of parana, brazil submission. Merge pdf, split pdf, compress pdf, office to pdf, pdf to jpg and more. Choroidal osteoma co is a rare, ossifying benign tumor originated in the choroid that typically occurs in otherwise healthy young women 1,2. Choroidal osteoma is a benign tumor of the choroid composed of mature bone. Two eyes of a patient with choroidal osteoma underwent complete ophthalmic examination. Choroidal osteoma, a benign tumor of mature bone, first appeared in a textbook in 1963 but was misdiagnosed as a calcified choroidal hemangioma reese 1963.
Multimodal imaging in choroidal osteoma international. On examination of the retina, it appears as an orangeyellow lesion usually located near the optic disc, often bilaterally. This rare, benign choroidal tumour is being recognized with increasing frequency, and is important to remember in the differential diagnosis of any unusual mass in the ocular fundus lest it be mistaken for a more sinister lesion. It is typically found in healthy young females in the second or third decades of life fig. In the hand, osteoid osteoma is more commonly located in the phalanges and carpal bones. The diagnosis is mainly clinical and relies on the appearance of the lesion on the examination of the posterior pole. A rare, benign tumor of the eye, composed of calcified bone. In contrast to other types of intraocular ossification, choroidal osteoma is found typically in young.
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