|Year : 2011 | Volume
| Issue : 3 | Page : 246-248
Temporary exudative retinal detachment following photodynamic therapy in a patient with retinal capillary hemangioblastoma
Ozlem Barut Selver, Aylin Yaman, Ali Osman Saatci
Department of Ophthalmology, Dokuz Eylul University, Izmir, Turkey
|Date of Web Publication||20-Aug-2011|
Ozlem Barut Selver
Emlakbank Konutlari, 73. Sokak A25/11 Blok, Daire No:3, Gaziemir, Izmir, 35410
Source of Support: None, Conflict of Interest: None
| Abstract|| |
A 21-year-old male with von Hippel-Lindau syndrome was treated for a retinal hemangioblastoma with photodynamic therapy (PDT). We employed the standard PDT protocol with doubled treatment duration. Seven days after the procedure, there were some perilesional intra- and subretinal hemorrhages and significant exudative retinal detachment extending inferiorly. Four weeks later, the hemorrhages had mostly cleared, and diminished subretinal fluid and partial regression of the hemangioblastoma were noted. PDT might induce temporary subretinal fluid accumulation in eyes with retinal hemangiomas.
Keywords: Photodynamic Treatment, Retinal Capillary Hemangioblastoma, Retinal Detachment
|How to cite this article:|
Selver OB, Yaman A, Saatci AO. Temporary exudative retinal detachment following photodynamic therapy in a patient with retinal capillary hemangioblastoma. Middle East Afr J Ophthalmol 2011;18:246-8
|How to cite this URL:|
Selver OB, Yaman A, Saatci AO. Temporary exudative retinal detachment following photodynamic therapy in a patient with retinal capillary hemangioblastoma. Middle East Afr J Ophthalmol [serial online] 2011 [cited 2020 Sep 29];18:246-8. Available from: http://www.meajo.org/text.asp?2011/18/3/246/84058
| Introduction|| |
Retinal capillary hemangioblastoma may occur sporadically either as an isolated lesion or as the first manifestation of von Hippel-Lindau (VHL) syndrome.  The natural course of retinal capillary hemangiomas can show progression, stability, or spontaneous regression.  However, in most eyes, varying amounts of intra- and subretinal hard exudates, epiretinal membrane and tractional retinal detachment, and secondary glaucoma may ensue during the course of the disease. Photodynamic therapy (PDT) has been performed in these cases with moderate success.
| Case Report|| |
A 21-year-old otherwise healthy man presented with visual loss in the left eye of 4 months' duration. His best corrected visual acuity was 20/20 in the right eye and 20/100 in the left eye. Slit-lamp examination and intraocular pressure were normal in both eyes. On funduscopy, there was a retinal capillary hemangioblastoma, approximately two disc diameters in size, in the inferior temporal quadrant, with prominent feeder vessels and submacular exudation in left eye [Figure 1]. Fluorescein angiography showed the classic signs of hemangioma. The patient had no family history of VHL syndrome. A systemic examination for VHL syndrome was negative but genetic testing for VHL syndrome turned out to be positive. We elected to proceed with PDT as the initial treatment. Intravenous verteporfin (6 mg/m  ) (Visudyne® ; Novartis AG, Basel, Switzerland) was administered over a 10-minute period. Five minutes after the completion of infusion, laser was delivered over the tumor at an intensity of 600 mW/cm  using a Reichel-Mainster 2 lens (Ocular Instruments, Bellevue, WA, USA) and 6000 μm spot size. Treatment duration was 166 seconds. The feeder vessel was intentionally not treated. At the first follow-up visit, 7 days after the procedure, there were some perilesional intra- and subretinal hemorrhages and significant exudative retinal detachment extending inferiorly [Figure 2]. After 4 weeks, the hemorrhages had partially cleared and the subretinal fluid had diminished substantially [Figure 3]. The hemangioblastoma had slightly decreased in size, with some fibrosis.
|Figure 1: Composite color picture of fundus shows a two-disc-diameter retinal angioma with feeder and draining vessels and macular exudation|
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|Figure 2: Composite color picture of fundus taken a week after photodynamic therapy shows the perilesional intra- and sub-retinal hemorrhage as well as the exudative retinal detachment extending inferiorly|
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|Figure 3: Color picture of fundus taken 4 weeks after photodynamic therapy shows fewer hemorrhages, diminished subretinal fl uid, and partially regressed hemangioblastoma|
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| Discussion|| |
PDT is still a valid treatment option for retinal hemangiomas. ,,,, While some authors prefer the standard protocol used in wet age-related macular degeneration, ,,, others use modified PDT protocols such as halving the infusion time to 5 minutes  and/or prolonging the exposure , to 166 seconds. PDT is either applied over the tumor and/or the feeding and draining vessels. 
Several complications following PDT have been reported previously in eyes with retinal angiomatosis. For example, increased traction may occur after PDT and there may even be tractional retinal detachment, requiring vitreoretinal surgery.  However, an increase in traction may also occur due to the normal progression of the disease. On the other hand, acute exudative detachment following PDT is rarely reported in eyes with retinal angiomatosis. Wong et al. treated a solitary retinal hemangioblastoma with standard age-related macular degeneration PDT protocol and reported that a week later there was increased macular edema, subretinal hemorrhage, and exudative retinal detachment surrounding the hemangioma. The subretinal fluid completely resolved after 5 weeks. The authors proposed that exudative detachment might be the result of increased leakage from the tumor or breakdown of the vascular barrier due to PDT-induced shutdown of the choriocapillaris and retinal capillaries. Szabo et al. described a patient with a large retinal angioma that was treated with standard PDT protocol. A day after PDT treatment, subretinal fluid had accumulated under the macula, but this subsided spontaneously within 12 days.
The standard PDT regimen is often somewhat arbitrarily modified in cases with various vascular tumors. We have preferred a prolonged exposure time of 166 seconds and have obtained successful outcomes in optic disc hemangioma, secondary vasoproliferative tumor, and vascularized granuloma. ,, However, prolonged exposure time might have been the cause of the exaggerated response of subretinal exudation in the present case.
In summary, one must be cognizant of the fact that the temporary exudative retinal detachment seen following PDT in eyes with retinal angiomatosis can occur without adverse long-term sequelae.
| References|| |
|1.||Singh AD, Shields CL, Shields JA. von Hippel-Lindau disease. Surv Ophthalmol 2001;46:117-42. |
|2.||Magee MA, Kroll AJ, Lou PL, Ryan EA. Retinal capillary hemangiomas and von Hippel-Lindau disease. Semin Ophthalmol 2006;21:143-50. |
|3.||Aaberg TM Jr, Aaberg TM Sr, Martin DF, Gilman JP, Myles R. Three cases of large retinal capillary hemangiomas treated with verteporfin and photodynamic therapy. Arch Ophthalmol 2005;123:328-32. |
|4.||Atebara NH. Retinal capillary hemangioma treated with verteporfin photodynamic therapy. Am J Ophthalmol 2002;134:788-90. |
|5.||Wong YM, Jalil A, Mathews J, Stanga PE. Exudative retinal detachment following photodynamic therapy for retinal capillary hemangioma. Can J Ophthalmol 2010;45:1-2. |
|6.||Suh SC, Jin SY, Bae SH, Kim CG, Kim JW. Retinal capillary hemangioma treated with verteporfin photodynamic therapy and intravitreal triamcinolone acetonide. Korean J Ophthalmol 2007;21:178-84. |
|7.||Bakri SJ, Sears JE, Singh AD. Transient closure of a retinal capillary hemangioma with verteporfin photodynamic therapy. Retina 2005;25:1103-4. |
|8.||Szabó A, Géhl Z, Seres A. Photodynamic (verteporfin) therapy for retinal capillary hemangioma, with monitoring of feeder and draining blood vessel diameters. Acta Ophthalmol Scand 2005;83:512-3. |
|9.||Yaman A, Saatci AO, Arikan G, Gunduz K. Involution of endophytic optic disc hemangioma with a single session of photodynamic treatment. Ann Ophthalmol (Skokie) 2007;39:63-6. |
|10.||Saatci AO. Yaman A. Arıkan G. Celikel H. Photodynamic treatment of a secondary vasoproliferative tumor associated with sector retinitis pigmentosa and Usher type I. Clin Exp Ophthalmo1 2007;35:191-3. |
|11.||Saatci AO, Selver OB, Yaman A, Arikan G, Sayiner A, Akkoclu A. Photodynamic therapy as an adjunct to systemic treatment in a case with unilateral presumed vascularized choroidal tuberculous granuloma. Int Ophthalmol 2009;29:293-6. |
[Figure 1], [Figure 2], [Figure 3]