CMV retinitis in a stem cell transplant recipient treated with foscarnet intravitreal injection and CMV specific immunoglobulins

Author:

Vassallo Francesco1,Nuzzi Raffaele2,Cattani Ilaria2,Dellacasa Chiara3,Giaccone Luisa3,De Rosa Francesco Giuseppe4,Cavallo Rossana56,Iovino Giorgia1,Brunello Lucia3,Bruno Benedetto3,Busca Alessandro7ORCID

Affiliation:

1. Department of Oncology and Hematology, AOU Citta’ della Salute e della Scienza, Turin, Italy

2. Eye Clinic Section, Department of Surgical Sciences, University of Turin, Italy

3. Stem Cell Transplant Center, AOU Citta’ della Salute e della Scienza, Turin, Italy

4. Department of Medical Sciences, University of Turin, Italy

5. SC Microbiology and Virology, A.O.U. Città della Salute e della Scienza di Torino, Torino, Italy

6. Department of Public Health and Pediatrics, University of Torino, Torino, Italy

7. Stem Cell Transplant Center, AOU Citta’ della Salute e della Scienza, Corso Bramante 88, Turin, 10126, Italy

Abstract

Cytomegalovirus (CMV) retinitis (CMVR) has been reported rarely in patients undergoing allogeneic hematopoietic stem cell transplantation (HSCT). In addition, little is known about strategies for ophthalmic surveillance and adequate antiviral treatment of CMVR. A case of CMVR in an allogeneic HSCT recipient is described, including clinical signs and therapy. An adult patient received HSCT from a matched unrelated donor for treatment of a Burkitt lymphoma. Donor and recipients were both CMV positive. Starting on day +40, the patient presented multiple CMV reactivation, treated with valganciclovir, foscarnet and a combination of both. On day +160, the patient started complaining of conjunctival hyperaemia and a decrease in visual acuity. Fundoscopy revealed retinal lesions consistent with CMVR, although whole blood CMV DNAemia was negative. Aqueous humor biopsy showed the presence of CMV infection (CMV DNA 230400 UI/ml). CMVR was treated with foscarnet (180 mg i.v. and 1.2 mg intravitreal injection) combined with anti CMV immunoglobulin at 0.5 ml/kg every 2 weeks. After 4 weeks of systemic therapy, 20 weekly doses of intravitreal foscarnet and six cycles of immunoglobulins, a significant improvement of visual acuity was observed. The treatment was well tolerated with no side effect. In conclusion, our case suggests that systemic and local antiviral treatment combined with CMV-specific-IVIG, may reduce CMV load in the eye of patients with CMVR, leading to a consistent improvement of visual acuity. Systematic ophthalmologic examination should be recommended in HSCT recipients with multiple CMV reactivations and high peak CMV DNA levels.

Publisher

SAGE Publications

Subject

Hematology

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