A 56-year-old man presented with a 2 day history of reduced left vision
Case History
A 56-year-old man presented complaining of acute loss of left vision the previous day. He had a history of T cell lymphoma with secondary haemophagocytic syndrome and was on high dose dexamethasone and etoposide. Systemically he was febrile with a low neutrophil count (neutropaenic).
On examination, his right vision was 6/6 and left vision 6/60. There were no cells in either anterior chamber. Intraocular pressures were 15mmHg each eye. There was mild left vitritis. Dilated examination of the right fundus revealed an occasional cotton wool spot. Examination of the left fundus is shown in Figure 1. There is evidence of retinitis with haemorrhage affecting the macula.
What is your diagnosis?
Differential diagnosis
The causes of acute retinal necrosis (ARN) in an immunocompromised patient include:
The cotton wool spots in the fellow eye are most likely due to the patient’s concurrent anaemia.
Initial treatment
Diagnosis
Figure 2.
Initially the area of retinal necrosis increased.
Clinical course
The patient remained systemically unwell due to his coexistent lymphoma and unfortunately, he passed away within 3 months of this presentation.
Discussion
CMV is a double stranded DNA Herpes virus. CMV is ubiquitous but is an opportunistic infection affecting patients who are immunocompromised. CMV retinitis is most commonly associated with patients with HIV and a CD4 count less than 50. Treatment for HIV normally increases the CD4 count whereby a patient’s own immunity can keep ocular CMV in remission. Because CMV can affect patients systemically, including colitis, pneumonitis and encephalitis, patients who are immunosuppressed post solid organ transplants often take medication for CMV prophylaxis. As with this patient, CMV retinitis can also occur in patients with lymphoma and also in patients with autoimmune disorders on high dose corticosteroids or on steroid-sparing immunosuppressive agents.
Ophthalmic features include retinitis in one or both eyes. Associated haemorrhage is common. Most commonly retinitis starts in the peripheral retina, but as in this case, it may present in the macular region. Vitritis is typically mild or absent but there may be associated vasculitis or a “frosted branch’’ appearance. It can also present as a granular retinitis which can be subtle.
Complications include retinal detachment especially for peripheral lesions. Systemic therapy is essential to prevent fellow eye involvement and extraocular infection.
First line treatment is induction with intravitreal foscarnet and/or intravitreal ganciclovir and intravenous ganciclovir 5mg/kg bd for 2 weeks followed by oral valganciclovir. Side effects include bone marrow suppression and neutropenia.
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