Vassallo Francesco, Nuzzi Raffaele, Cattani Ilaria, Dellacasa Chiara, Giaccone Luisa, De Rosa Francesco Giuseppe, Cavallo Rossana, Iovino Giorgia, Brunello Lucia, Bruno Benedetto, Busca Alessandro
Department of Oncology and Hematology, AOU Citta' della Salute e della Scienza, Turin, Italy.
Eye Clinic Section, Department of Surgical Sciences, University of Turin, Italy.
Ther Adv Hematol. 2020 Dec 10;11:2040620720975651. doi: 10.1177/2040620720975651. eCollection 2020.
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.
巨细胞病毒(CMV)视网膜炎(CMVR)在接受异基因造血干细胞移植(HSCT)的患者中鲜有报道。此外,关于CMVR的眼科监测策略和充分的抗病毒治疗知之甚少。本文描述了1例异基因HSCT受者发生CMVR的病例,包括临床症状和治疗情况。1例成年患者接受了来自匹配无关供者的HSCT,用于治疗伯基特淋巴瘤。供者和受者均为CMV阳性。在移植后第40天,患者出现多次CMV再激活,先后接受了缬更昔洛韦、膦甲酸钠及两者联合治疗。在移植后第160天,患者开始抱怨结膜充血和视力下降。眼底检查发现视网膜病变符合CMVR,尽管全血CMV DNA血症为阴性。房水活检显示存在CMV感染(CMV DNA 230400 UI/ml)。CMVR采用膦甲酸钠(静脉注射180 mg和玻璃体内注射1.2 mg)联合抗CMV免疫球蛋白,每2周0.5 ml/kg进行治疗。经过4周的全身治疗、20次每周1次的玻璃体内膦甲酸钠注射和6个周期的免疫球蛋白治疗后,视力有显著改善。治疗耐受性良好,无副作用。总之,我们的病例表明,全身和局部抗病毒治疗联合CMV特异性静脉注射免疫球蛋白,可能降低CMVR患者眼部的CMV载量,从而使视力持续改善。对于多次发生CMV再激活且CMV DNA峰值水平较高的HSCT受者,应建议进行系统的眼科检查。