J Korean Ophthalmol Soc.  2008 Mar;49(3):531-538. 10.3341/jkos.2008.49.3.531.

A Case of Valganciclovir Treatment for Cytomegalovirus Retinitis

Affiliations
  • 1Department of Ophthalmology, Inha University School of Medicine, Incheon, Koera.
  • 2Ophthalmologic Oncology Clinic, National Cancer Center, Gyeonggi, Korea. dreye@freechal.com

Abstract

PURPOSE: To report a case of a patient with cytomegalovirus (CMV) retinitis who was treated with oral valganciclovir.
CASE SUMMARY
A 34-year-old man who had undergone anti-cancer chemotherapy for Non-Hodgkin lymphoma was referred to the ophthalmologic oncology clinic because of decreased vision in both eyes. Fundus examination showed white, opaque, and granular retinal lesions in both eyes, and a serologic test showed a positive response to CMV antibody IgG and a negative response to CMV antibody IgM. The patient received induction therapy with intravenous ganciclovir and maintenance therapy with oral valganciclovir 900 mg once daily. CMV retinitis reactivated 4 weeks after maintenance therapy was discontinued. At that point, the patient received induction therapy with oral valganciclovir 900 mg twice daily for 3 weeks and maintenance therapy with 900 mg once daily for 5 weeks. The retinal lesion disappeared and did not recur after oral administration of valganciclovir. The patient discontinued valganciclovir after 5 weeks of maintenance therapy, and CMV retinitis did not reactivate during 6 months of follow-up.
CONCLUSIONS
Oral valganciclovir was clinically effective in the treatment of CMV retinitis in a patient who was treated with anti-cancer chemotherapy for non-Hodgkin lymphoma.

Keyword

Cytomegalovirus Retinitis; Ganciclovir; Valganciclovir

MeSH Terms

Administration, Oral
Adult
Cytomegalovirus
Cytomegalovirus Retinitis
Eye
Follow-Up Studies
Ganciclovir
Humans
Immunoglobulin G
Immunoglobulin M
Lymphoma, Non-Hodgkin
Retinaldehyde
Retinitis
Serologic Tests
Vision, Ocular
Ganciclovir
Immunoglobulin G
Immunoglobulin M
Retinaldehyde

Figure

  • Figure 1. Fundus photographs and fluorescein angiogram at the first visit. (A) Fundus photograph of the right eye shows white, opaque, irregular, and granular lesions superior to the fovea and superotemporal vascular arcade. (B) Fundus photograph of the left eye shows granular and small satellites appearance at the linear advanced border in the superotemporal portion. (C, D) Fluorescein angiogram of right eye at the early phase shows mild staining, and left eye shows linear retinal border of hypofluorescence. (E, F) Fluorescein angiogram of both eyes at the late phase show diffuse dye leakage from the previously hypo- or hyperfluorescence lesions.

  • Figure 2. Fundus photographs after intravenous ganciclovir as induction therapy and oral valganciclovir as maintenance therapy.(A, B) After 2 weeks of intravenous ganciclovir as induction therapy, the granular lesions have decreased and the lesion border not advanced. (C, D) After 2 weeks of oral valganciclovir as maintenance therapy, the lesions have much decreased. Retinal vascular sheathing observed at the superotemporal portion of the left eye.

  • Figure 3. Fundus photographs following reactivation of CMV retinitis. (A, B) CMV retinitis lesion following reactivation at 4 weeks after intravenous ganciclovir as induction therapy and oral valganciclovir as maintenance therapy were discontinued. The lesion border advanced more anteriorly and in circumferential directions than in the first attack. (C, D) After 2 weeks of oral valganciclovir as maintenance therapy, the granular lesions became less opacified. The area of infected retinal tissue has been replaced by a thin, gliotic scar, with the fine mottling of the retinal pigment epithelium.


Cited by  1 articles

Cinical Manifestations and Prognosis of Cytomegalovirus Retinitis
Young Kyo Kwun, Ju Byung Chae, Don Il Ham
J Korean Ophthalmol Soc. 2010;51(2):203-209.    doi: 10.3341/jkos.2010.51.2.203.


Reference

References

1. Egbert PR, Pollard Rb, Gallagher JG, et al. Cytomegalovirus retinitis in immunosuppressed hosts. II. Ocular manifestations. Ann Intern Med. 1980; 93:664–70.
2. Pescoviz MD, Rabkin J, Merion RM, et al. Valganciclovir results in improved oral absorption of ganciclovir in liver transplant recipients. Antimicrob Agents Chemother. 2000; 44:2811–5.
Article
3. Limaye AP, Corey L, Koelle DM, et al. Emergence of ganciclovir-resistant cytomegalovirus disease among recipients of solid-organ transplants. Lancet. 2000; 356:645–9.
Article
4. Markham A, Faulds D. Ganciclovir. An update of its therapeutic use in cytomegalovirus infection. Drugs. 1994; 48:455–84.
5. Pescovitz MD, Pruett TI, Gonwa T, et al. Oral ganciclovir dosing in transplant recipients and dialysis patients based on renal function. Transplantation. 1998; 66:1104–7.
6. Bartlett JG. The Johns Hopkins Hospital 1997 guide to medical care of patients with HIV infection. 7th ed.Baltimore: Williams & Wilkins;1997. p. 107–9.
7. Einsele H, Reusser P, Bornhauser M, et al. Oral valganciclovir leads to higher exposure to ganciclovir than intravenous ganciclovir in patients following allogeneic stem cell transplantation. Blood. 2006; 107:3002–8.
Article
8. Faulds D, Heel RC. Ganciclovir. A review of its antiviral activity, pharmacokinetic properties and therapeutic efficacy in cytomegalovirus infections. Drugs. 1994; 48:455–84.
9. Hamzeh FM, Literman PS. Intranuclear accumulation of sub-genomic noninfectious human cytomegalovirus DNA in infected cells in the presence of ganciclovir. Antimicrob Agents Chemother. 1991; 35:1818–23.
Article
10. Jung D, Dorr A. Single-dose pharmacokinetics of valganciclovir in HIV- and CMV-seropositive subjects. J Clin Pharmacol. 1999; 39:800–4.
Article
11. Brown F, Banken L, Saywell K, Arum I. Pharmoacokinetics of valganciclovir and ganciclovir following multiple oral dosages of valganciclovir in HIV- and CMV-serppositive volunteers. Clin Pharmacokinet. 1999; 37:167–76.
12. Martin DF, Sierra-Madero J, Walmsley S, et al. A controlled trial of valganciclovir as induction therapy for cytomegalovirus retinitis. N Engl J Med. 2002; 346:1119–26.
Article
13. Kim IT, Lim JH, Seo HD. Ganciclovir treatment for cytomegalovirus retinitis in renal transplant recipients. J Korean Ophthalmol Soc. 1997; 38:242–50.
14. Holland GN, Sidikaro Y, Kreiger AE, et al. Treatment of cytomegalovirus retinopathy with ganciclovir. Ophthalmology. 1987; 94:815–23.
Article
15. Jabs DA, Newman C, de Bustros S, et al. Treatment of cytomegalovirus retinitis with ganciclovir. Ophthalmology. 1987; 94:824–30.
Article
16. Kim YH, Kim SK. Cytomegalovirus retinitis in a child with acute lymphoblastic leukemia. J Korean Ophthalmol Soc. 2006; 47:1009–15.
17. Polland RB, Egbert PR, Gallagher JG, Merigan TC. Cyto-megalovirus retinitis in immunosuppressed hosts. I. Natural history and effects of treatment with adenine arabinoside. Ann Intern Med. 1980; 93:655–64.
18. Meredith TA, Aaberg TM, Resser FH. Rhegmatogenous retinal detachment complicating cytomegalovirus retinitis. Am J Ophthalmol. 1979; 87:793–6.
Article
19. Erice A, Jordan MC, Chace BA, et al. Ganciclovir treatment of cytomegalovirus disease in transplant recipients and other immunocompromised hosts. JAMA. 1987; 12:3082–7.
Article
20. Harbison MA, DeGirolami PC, Jenkins RL, et al. Ganciclovir therapy of severe cytomegalovirus infections in solid organ transplant recipients. Transplantation. 1988; 46:82–8.
21. Banmal CR, Levin AV, Read SE, et al. Cytomegalovirus retinitis in immunosupressed children. Am J Ophthalmol. 1999; 127:550–8.
22. Park MY, Ohn YH, Park SH. Three cases of cytomegalovirus retinitis in the immunosupressed kidney transplant patients. J Korean Ophthalmol Soc. 1993; 34:918–23.
23. Yi WM, Kim MH, Yoo JS, Huh W. CMV papillitis in renal transplant recipient. J Korean Ophthalmol Soc. 1998; 39:2768–71.
24. Cho CW, Park YM, Seo MS. Effect of ganciclovir on cytomegalovirus retinitis of a renal transplant patient without maintenance therapy. J Korean Ophthalmol Soc. 1997; 38:637–42.
25. Lalezari J, lindely J, Walmsley S, et al. A safety study of oral valganciclovir maintenance treatment of cytomegalovirus retinitis. J Acquir Immune Defic Syndr. 2002; 30:392–400.
Article
Full Text Links
  • JKOS
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr