Korean J Ophthalmol.  2007 Sep;21(3):178-184. 10.3341/kjo.2007.21.3.178.

Retinal Capillary Hemangioma Treated with Verteporfin Photodynamic Therapy and Intravitreal Triamcinolone Acetonide

Affiliations
  • 1Department of Ophthalmology, College of Medicine, Konyang University, Myung Gok Eye Research Institute, Daejeon, Korea. ophthal73@hanmail.net

Abstract

PURPOSE: To report a case of retinal capillary hemangioma treated with verteporfin photodynamic therapy combined with intravitreal triamcinolone acetonide. METHODS: A 15-year-old female presented with metamorphopsia in the left eye for 7 days. Examination showed peripheral endophytic retinal capillary hemangioma, macular edema, and a best-corrected visual acuity of 20/50. The hemangioma and macular edema were treated with verteporfin photodynamic therapy and intravitreal triamcinolone acetonide. RESULTS: After 5 months of follow-up, involution of the hemangioma, reduction of macular edema, decrease of the feeder and draining vessel diameter, and improvement of best-corrected visual acuity to 20/25 was seen. CONCLUSIONS: This verteporfin photodynamic therapy combined with intravitreal triamcinolone acetonide appeared to cause involution of the hemangioma with reduction in macular edema and improvement in visual acuity.

Keyword

Retinal Capillary Hemangioma; Triamcinolone Acetonide; Vertepofin Photodynamic Therapy

MeSH Terms

Adolescent
Female
Fundus Oculi
Glucocorticoids/*administration & dosage/therapeutic use
Hemangioma, Capillary/diagnosis/*drug therapy
Humans
Injections
*Photochemotherapy
Photosensitizing Agents/*therapeutic use
Porphyrins/*therapeutic use
Retinal Neoplasms/diagnosis/*drug therapy
Tomography, Optical Coherence
Triamcinolone Acetonide/*administration & dosage/therapeutic use
Ultrasonography
Vitreous Body

Figure

  • Fig. 1 First visit (pre-treatment). (A) The left fundus reveals mild macular edema and hard exudates with tortuous dilated vessel. (B) Circumscribed endophytic retinal capillary hemangioma appears at the 5 o'clock periphery with a prominent dilated and tortuous feeding artery and draining vein. (C, D) Progressive and complete filling of the hemangioma and the retinal vein becomes prominent. (E) OCT image demonstrating cystic macular edema at first visit. (F) B-scan shows a well-demarcated endophytic retinal lesion without choroidal effects.

  • Fig. 2 Optical coherence tomogram images. (A) OCT image demonstrating cystic macular edema at first visit. (B) Worsened cystic macular edema after PDT treatment. (C) 12 days after PDT, improvement of cystic intraretinal edema after intravitreal triamcinolone acetonide. (D) 22 days after PDT, OCT image of the forvea shows restoration of the foveal contour.

  • Fig. 3 12 days after PDT. (A) The feeder and draining vessel diameters decreased. (B) The retinal capillary hemangioma underwent partial involution (approximately 2.5 DD). The whitish mass is triamcinolone acetonide.

  • Fig. 4 22 days after PDT. (A) The left fundus reveals decreased macular edema and hard exudates with a straighter vessel. (B) The retinal capillary hemangioma regressed approximately 1.5 DD. (C, D) Fluorscein angiogram demonstrating decreased early filling and late leakage of the hemangioma. (E) B-scan showing decreased endophytic retinal lesion.

  • Fig. 5 3 months after PDT. (A) The macular hard exudate and edema improved. (B) The retinal capillary hemangioma regressed approximately 1.0 DD.

  • Fig. 6 5 months after PDT. (A) The macular hard exudate and edema nearly disappeared. (B) Fluorescein angiogram demonstrating reduced fluorescence and leakage associated with the lesion.


Cited by  1 articles

Clinical Results of Various Treatments for Retinal Capillary Hemangioma
Yeo-Kyoung Won, Min-Woo Lee, Yong-Il Shin, Jung-Yeul Kim, Young-Joon Jo
Korean J Ophthalmol. 2020;34(2):133-142.    doi: 10.3341/kjo.2019.0075.


Reference

1. Singh AD, Nouri M, Shield CL, et al. Retinal capillary hemangioma: a comparison of sporadic cases and cases associated with von Hippel-Lindau disease. Ophthalmology. 2001. 108:1907–1911.
2. Singh AD, Shields CL, Shields JA. von Hippel-Lindau disease. Surv Ophthalmol. 2001. 46:117–142.
3. Moskowitz C, Edelstein C, Oh M, et al. Retinal capillary hemangioma in von Hippel-Lindau disease. Can J Ophthalmol. 2005. 40:192–194.
4. Ryan SJ. Hinz BJ, Schachat AP, editors. Capillary hemangioma of the retina and von Hippel-Lindau diease. Retina. 2006. v.1:4th ed. Mosby: Elsevier Inc.;chap. 24.
5. Gass JDM. Stereoscopic atlas of macular disease. Diagnosis and treatment. 1997. 4th ed. St. Louis: Mosby;850–865.
6. Ridley M, Green J, Johnson G. Retinal angiomatosis: the ocular manifestations of von Hippel-Lindau disease. Can J Ophthalmol. 1986. 21:276–283.
7. Mcdonald HR, Schatz H, Johnson RN, et al. Vitrectomy in eyes with peripheral retinal angioma associated with traction macular detachment. Ophthalmology. 1996. 103:329–335.
8. Rodriguez-Coleman H, Spaide RF, Yannuzzi LA. Treatment of angiomatous lesions of the retina with photodynamic therapy. Retina. 2002. 22:228–232.
9. Photodynamic therapy of subfoveal choroidal neovascularization in age-related macular degeneration with verteporfin. Arch Ophthalmol. 1999. 117:1329–1345.
10. Verteporfin in Photodynamic Therapy Study Group. Verteporfin therapy of subfoveal choroidal neovascularization in age-related macular degeneration: two-year results of a randomized clinical trial including lesions with occult with no classic choroidal neovascularization-verteporfin in photodynamic therapy report 2. Am J Ophthalmol. 2001. 131:541–560.
11. Singh AD, Shields JA, Shields CL. Solitary retinal capillary hemangioma: hereditary (von Hippel-Lindau disease) or non hereditary? Arch Ophthalmol. 2001. 119:232–234.
12. Webster AR, Maher ER, Bird AC, Moore AT. Risk of multisystem disease in isolated ocular angioma (haemangioblastoma). J Med Genet. 2000. 37:62–63.
13. Annesley WH Jr, Leonard BC, Shield JA, et al. Fifteen year review of treated cases of retinal angiomatosis. Trans Am Acad Ophthalmol Otolaryngol. 1977. 83:446–453.
14. Ridley M, Green J, Johnson G. Retinal angiomatosis: the ocular manifestations of von Hippel-Lindau disease. Can J Ophthalmol. 1986. 21:276–283.
15. Shields JA, Shields CL. Intraocular tumors, A text and atlas. 1992. Philadelphia: WB Saunders;393–419.
16. Husain D, Gragoudas ES, Miller JW. Principles and practice of ophthalmology. 2000. 2nd ed. Philadelphia: WB Saunders;577–587.
17. Gass JDM. Treatment of retinal vascular anomalies. Trans Am Acad Ophthalmol Otolaryngol. 1977. 83:432–442.
18. Welch RB. von Hippel-Lindau disease: the recognition and treatment of early angiomatosis retinae and the use of cryosurgery as an adjunct to therapy. Trans Am Ophthalmol Soc. 1970. 68:367–424.
19. Atebara NH. Retinal capillary haemangioma treated with verteporfin photodynamic therapy. Am J Ophthalmol. 2002. 134:788–790.
20. Ryan SJ. Hinz BJ, Schachat AP, editors. Capillary hemangioma of the retina and von Hippel-Lindau diease. Retina. 2006. v. 1:4th ed. Mosby: Elsevier Inc.;chap. 65.
21. Spaide RF, Sorenson J, Maranan L. Combined photodynamic therapy with verteporfin and intravitreal triamcinolone acetonide for choroidal neovascularization. Ophthalmology. 2003. 110:1517–1525.
22. Ryan SJ. Hinz BJ, Schachat AP, editors. Capillary hemangioma of the retina and von Hippel-Lindau diease. Retina. 2006. v. 1:4th ed. Mosby: Elsevier Inc.;chap. 55.
23. Penfold PL, Wen L, Madigan MC, et al. Modulation of permeability and adhesion molecules expression by human choroidal endothelial cells. Invest Ophthalmol Vis Sci. 2002. 3125–3130.
24. Wang YS, Friedrichs U, Eichler W, et al. Inhibitory effects of triamcinolone acetonide on bFGF-induced migration and tube formation in choroidal microvascular endothelial cells. Graefes Arch Clin Exp Ophthalmol. 2002. 240:42–48.
25. Ciulla TA, Criswell MH, Danis RP, Hill TE. Intravitreal triamcinolone acetonide inhibits choroidal neovascularization in a laser-treated rat model. Arch Ophthalmol. 2001. 119:399–404.
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