Primary central nervous system lymphoma presenting as bilateral uveitis in an immunocompetent hepatitis C virus+ patient: a case report
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To report a case of masquerade syndrome presenting as bilateral uveitis in an HCV positive patient, and to highlight the difficulties in distinguishing between chronic uveitis and malignancy-induced inflammation.
In January 2005 a 54-year-old Caucasian man was referred to the Ophthalmological Department for bilateral visual loss, severe vitritis, and a significant cataract in both eyes. His clinical history was significant for HCV infection. The uveitis treated with low dose of steroids and immunosuppressors, yielding a partial remission of the symptoms. One year later he developed a Primary Central Nervous System Lymphoma. In January 2007 he returned to our department for cataract surgery. The patient underwent phacoemulsification of the cataract in the right eye, intraocular lens implantation and intravitreal injections of 4 mg triamcinolone acetonide. After one month fundus biomicroscopy showed a solid lesion at the posterior pole, consistent with a retinal relapse of the Primary Central Nervous System Lymphoma. Restaging investigations were unremarkable and ruled out a disease relapse, and a diagnostic vitrectomy showed only rare inflammatory cells. In view of the progressive swelling of the retinal lesions we decided to treat the patient with intravitreal Methotrexate. Complete remission of the retinal lesions with retinal scarring was achieved after 12 months. In May 2008 the patient underwent phacoemulsification of the cataract in the left eye and intraocular lens implantation. A vitreal tap was performed and was positive for rare abnormal cells CD45+, CD20-. Vitreous sampling did not yield enough cells for a diagnosis of monoclonality. No systemic or intravitreal therapy was performed because of the absence of central nervous system relapses, the small number of atypical cells found in the vitreous sample and the absence of retinal masses. After three months the patient developed a central nervous system relapse of the lymphoma and rapidly died.
In elderly patients suffering from uveitis a masquerade syndrome should always be suspected. Vitreous sampling may not yield enough cells for diagnosis and the vitritis may be steroid-sensitive, at least initially. This makes a differential diagnosis between chronic uveitis and malignancy-induced inflammation very difficult.
KeywordsUveitis Primary Central Nervous System Lymphoma Triamcinolone Acetonide Central Nervous System Relapse Retinal Lesion
Primary Central Nervous Lymphoma
Primary Intra Ocular Lymphoma
The incidence of true immune-mediated uveitis declines in the elderly. Infection endophthalmitis, especially arising after surgery, and malignancy occur at higher frequency. In this age group, the suspicion of a masquerade syndrome, particularly a primary CNS non-Hodgkin's lymphoma, should always be raised . We describe a case of an immunocompetent HCV+ patient referred to the Ophthalmological Department of Bari University Hospital for bilateral uveitis. The inflammation, initially diagnosed as a complication of the chronic hepatitis C virus, was, instead, the first manifestation of a primary central nervous system lymphoma, that was diagnosed one year later.
In January 2005 a 54-year-old Caucasian immunocompetent man was referred to the Ophthalmological Department for bilateral visual loss (right eye: 20/100 and left eye: 20/60), severe vitritis, cells in the anterior chamber and a significant cataract in both eyes. In both eyes the intraocular pressure (IOP) was 15 mmHg.
His clinical history was significant for HCV infection treated with interferon, and for insulin dependent diabetes. The bilateral ocular uveitis was correlated to the HCV infection and treated with low dose of steroids and immunosuppressors, yielding a partial remission of the symptoms. One year later the patient developed neurological symptoms, (a slow-down in mental and motility performance and a central defect of the VII cranial nerve) that led to a cranial CT examination and to the diagnosis of Primary Central Nervous System Lymphoma (PCNSL) arising from the left nuclei of the base, the nucleus caudatus, the anterior arm of the internal capsule, the insula and thalamus(stereotaxically diagnosed as CD45+, CD20+, CD3neg, CD10neg, Td Tneg, ki-67/MIB-1 = 90%), treated with L-VAMP multi chemotherapy and radiotherapy, resulting incomplete recovery.
In January 2007 he returned to our department for a deterioration of the visual acuity(only light perception in the right eye and 20/200 in the left eye). He presented a total white cataract in the right eye and a severe cataract affecting the visus in the left eye. There were rare inflammatory cells in the anterior chamber of both eyes. Ultrasonographic examination showed a severe vitritis and a small, solid uplift at the posterior pole, misinterpreted as macula cystoids edema in the right eye and a mild vitritis in the left eye.
Restaging investigations (CT, MRI, spinal tap, osteomedullary biopsy) were unremarkable and ruled out a disease relapse, and a vitreal tap and subsequent diagnostic vitrectomy showed only rare inflammatory cells.
In May 2008 the patient underwent phacoemulsification of the cataract in the left eye and acrylic hydrophilic intraocular lens implantation. A vitreal tap was performed and was positive for rare abnormal cells CD45+, CD20-. Vitreous sampling did not yield enough cells for a diagnosis of monoclonality, the hallmark of malignant processes.
After one month, visual acuity in left eye was 20/20, there was a mild vitritis and no retinal lesions. A new restaging of the disease was performed and no relapse was detected. No systemic or intravitreal therapy was performed because of the absence of central nervous system relapses, the small number of atypical cells found in the vitreous sample and the absence of retinal masses.
Unfortunately, after three months the patient developed a central nervous system relapse of the lymphoma and rapidly died of the malignancy and the toxic effect of the new high dosage systemic chemotherapy.
Primary central nervous system lymphoma (PCNSL)accounts for 4 to 7% of brain tumours. It occurs with a markedly increased incidence in the immunosuppressed population but its incidence has increased in the past two decades in immunocompetent patients as well [4, 5, 6], probably due to the better diagnostic imaging and biopsy sampling methods available in recent years.
Primary intraocular lymphoma (PIOL), is a subset of primary central nervous system lymphoma (PCNSL), in which lymphoma cells invade the subretinal pigment epithelial space and vitreous cavity, with or without central nervous system involvement at the time of the ocular diagnosis. The age of onset of PIOL ranges from 15 to 85 years, with a mean age of the late 50s to early 60s. Both sexes are affected but most series point to a higher incidence in women.
Typical clinical symptoms of PIOL include blurred vision and floaters. In many of these patients uveitis is initially diagnosed, especially if there is no known history of cerebral involvement. The most common ophthalmic manifestations are similar to those seen in patients with posterior uveitis or vitreitis, combined anterior and posterior uveitis, or subretinal pigment epithelial infiltrates .
Without treatment, PIOL is often rapidly fatal, especially when associated with PCNSL. Currently, the five year survival rate ranges from less than 20% to 34% with the best therapy [8, 9]. It is imperative, then, to make a prompt diagnosis so that life extending treatment may be started. The diagnosis of intraocular lymphoma can be very difficult patients with intraocular lymphoma may seem perfectly well with no systemic or neurological symptoms and signs, peripheral blood, bone marrow cytology and cellular morphology are usually normal and therefore unhelpful. Ocular examination can be helpful, but the degree of vitritis is highly variable and retinal lesions may or may not be found. Even in the presence of retinal lesions, doing a biopsy is hazardous, may miss the lesion, and if successful, will only yield a small number of cells. A vitreous sample can also be unhelpful, as in our patient, because it will only yield a small number of atypical cells so it is not possible to determine the monoclonality, or it may yield only inflammatory cells. This makes the differentiation between chronic inflammation and intraocular lymphoma very difficult .
In our case, the diagnosis was delayed because initially the ocular inflammation was correlated to the hepatitis C. The patient presented only few ocular signs and seemed perfectly well, with no systemic or neurological symptoms and signs. Moreover, the ocular vitritis showed a partial response to the mild steroid and immunosuppressive therapy instituted.
Only one year later the patient developed neurological symptoms, (a slow-down in mental and motility performance and a central defect of the VII cranial nerve) that led to a cranial CT examination and to the diagnosis of central nervous system lymphoma.
When the correct diagnosis of the ocular pathology was made, after extracting the cataractin the right eye few therapeutic options were available, because the patent had just undergone systemic chemo and radiotherapy, and refused eye enucleation.
Intrathecal therapy was not recommended because of the complete absence of relapse of the CNS disease. Eye radiotherapy could cause eye dryness, actinic retinopathy, optic neuropathy and resulting irreversible severe visual loss.
The response to IMTX was fast and an improvement of the visual acuity and a regression of the retinal lesions were observed within 8 weeks. We did not observe any ophthalmic side effects such as corneal epitheliopathy, maculopathy, vitreous hemorrhage, optic atrophy or sterile endophthalmitis.
Despite the good results of the systemic chemotherapy, radiotherapy and intravitreal therapy in the right eye, and the negative results of all the precedent restaging examinations, after three months the patient developed a new, fatal PCNSL localization. This case confirms the very poor prognosis of these malignancies, especially in cases of relapse.
Written informed consent was obtained from the patient's son for the publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in Chief of this journal.
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