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Choroidal Osteoma Accompanied by Proliferative Diabetic Retinopathy

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© 2018 The Korean Ophthalmological Society

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses /by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

521

Choroidal Osteoma Accompanied by Proliferative Diabetic Retinopathy

Dear Editor,

Choroidal osteoma is an uncommon benign ossifying tu- mor involving the choroid and usually presents as an ele- vated choroidal lesion with round, ill-defined borders locat- ed in the juxtapapillary or macula region [1,2]. To date, the treatment for choroidal osteoma has not been established.

Herein, we describe a case of a patient who underwent in- travitreal ranibizumab injection for choroidal osteoma ac- companied by proliferative diabetic retinopathy.

A 49-year-old male who was treated for proliferative dia- betic retinopathy visited our clinic due to ocular pain in his right eye 4 days in duration. His past medical history in- cluded diabetes mellitus. His ophthalmic history showed high risk proliferative diabetic retinopathy in both eyes; the patient underwent photocoagulation at a local clinic. The initial best-corrected visual acuity was 0.04 in the right eye and 0.4 in the left eye. The initial intraocular pressure was 15 mmHg in the right eye and 14 mmHg in the left eye.

Two years ago he was diagnosed with diabetic macular edema and intravitreal aflibercept injection was performed

in our hospital. One month after the injection, subretinal fluid was completely absorbed. On slit-lamp examination, no abnormal findings were found except mild swelling in the right upper lid and diffuse hyperemia in the right con- junctiva. On fundus examination, a yellowish elevated le- sion was observed in the macula of his right eye (Fig. 1A).

Fluorescein angiography showed no leakage and mild staining at the perifoveal area at late phase (Fig. 1B). Our initial diagnosis was suspicious choroidal mass with diabet- ic macular edema in the right eye and upper lid preseptal cellulitis in the right eye. Therefore, ultrasonography and orbital computed tomography with enhancement were per- formed. Highly reflective echo and posterior acoustic shad- owing were observed in his right eye (Fig. 1C). Orbital computed tomography showed mild infiltration at the ante- rior ocular wall, asymmetrical swelling of lacrimal gland, and small calcification at posterior ocular wall (Fig. 1D, 1E). Optical coherence tomography (Spectralis, Heidelberg Engineering, Heidelberg, Germany) also showed an elevat- ed mass lesion and subretinal fluid with small choroidal neovascularization (CNV) in the right eye (Fig. 1F). The patient was prescribed oral antibiotics, levofloxacin eye- drops, and fluorometholone eyedrops.

After 2 days, upper lid swelling significantly decreased and conjunctival injection was improved. However, optical coherence tomography showed persistent subretinal fluid.

The patient was finally diagnosed with choroidal osteoma

Korean J Ophthalmol 2018;32(6):521-522 https://doi.org/10.3341/kjo.2018.0029

Fig. 1. (A) At fundus photography, yellowish elevated lesion with irregu- lar margin was noted. (B) On fluores- cein angiography, mild staining was observed for perifoveal area at late phase. (C) Highly reflective echo and posterior acoustic shadowing were observed in the ultrasonography. (D) Computed tomography showed mild infiltration at anterior ocular wall, asymmetrical swelling of lacrimal gland, and small calcification at posterior wall. (E) Computed tomog- raphy scan with bone density. (F) At initial examination, optical coherence tomography showed subretinal fluid with small choroidal neovasculariza- tion. (G) A month after intravitreal ranibizumab injection, subretinal fluid was completely absorbed.

A B C

D E

F

G

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Korean J Ophthalmol Vol.32, No.6, 2018

with subretinal fluid. Intravitreal ranibizumab (Novartis, East Hanover, NJ, USA) injection was performed (0.05 mL) and 1 month after the injection, subretinal fluid was com- pletely absorbed and visual acuity recovered from 0.04 to 0.2 (Fig. 1G).

Choroidal osteoma often occurs as a unilateral condition in young females and supposedly associated with congenital causes, inflammatory conditions, and endocrine disorders;

however, the origin is unclear [1]. Fluorescein angiography of choroidal osteoma shows punctate hyperfluorescence at early phase and diffuse staining at late phase. In addition, ultrasonography shows a strong reflection wave on the inner surface of the tumor and computed tomography shows radi- opacity in accordance with bone density.

The treatment for choroidal osteoma has not yet been es- tablished and the patient is usually under observation if there is no active lesion. However, various treatments have been attempted if CNV or subretinal fluid are present. Pre- viously, photocoagulation was typically used for extrafove- al CNV, and subfoveal CNV was treated with transpupil- lary thermotherapy or photodynamic therapy. However, there are many drawbacks such as limited final visual acui- ty. Recently, several cases were treated with anti-vascular endothelial growth factor drugs used in age-related macu- lar degeneration or diabetic macular edema such as bevaci- zumab or ranibizumab [3,4]. Najafabadi et al. [3] reported improvement in a patient treated with intravitreal bevaci- zumab for choroidal osteoma without CNV.

In our patient, subretinal fluid with small CNV was ob- served in the choroidal osteoma accompanied by prolifera- tive diabetic retinopathy. Improvement of subretinal fluid and visual acuity were observed 1 month after intravitreal ranibizumab injection. Therefore, we suggest that intravit- real ranibizumab injection may be a useful treatment for the subretinal fluid associated with choroidal osteoma.

Hyun Sup Choi, Yong-Kyu Kim, Sung Pyo Park

Department of Ophthalmology, Kangdong Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Korea E-mail (Sung Pyo Park): [email protected]

Conflict of Interest

No potential conflict of interest relevant to this article was reported.

Acknowledgements

This study was financially supported by Korean Associ- ation of Retinal Degeneration.

References

1. Alameddine RM, Mansour AM, Kahtani E. Review of cho- roidal osteomas. Middle East Afr J Ophthalmol 2014;21:244- 50.

2. Shields CL, Sun H, Demirci H, Shields JA. Factors predic- tive of tumor growth, tumor decalcification, choroidal neo- vascularization, and visual outcome in 74 eyes with choroi- dal osteoma. Arch Ophthalmol 2005;123:1658-66.

3. Najafabadi FF, Hendimarjan SM, Zarrin Y, Najafabadi MF.

Intravitreal bevacizumab for management of choroidal os- teoma without choroidal neovascularization. J Ophthalmic Vis Res 2015;10:484-6.

4. Pandey N, Guruprasad A. Choroidal osteoma with choroi- dal neovascular membrane: successful treatment with in- travitreal bevacizumab. Clin Ophthalmol 2010;4:1081-4.

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Fig. 1. (A) At fundus photography,  yellowish elevated lesion with  irregu-lar margin was noted

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