2 cases per 1000 patient-years, 95% CI: 0.8–1.9) than in the pre-HAART era (3.0 cases per 1000 patient-years, 95% CI: 2.1–4.0; p < 0.001), and overall survival is longer (median survival 32 days, range 5–315 days vs. 48 days, range 15–1136 days; log rank p = 0.03) [4]. Patients rarely present with B symptoms such as fever, weight loss, or night sweats that are commonly associated with other forms of NHL. PCNSL typically

presents with a focal mass lesion in more than 50% of cases. In 248 immunocompetent patients, 43% had neuropsychiatric signs, 33% had increased intracranial pressure, 14% had seizures, and 4% had ocular symptoms at the time of presentation [3]. The presentation of PCNSL in people living with HIV may be with subacute focal neurological signs [4]. Examination includes full medical, neurological and neuropsychological assessment. Investigations including serum LDH, selleck screening library CSF analysis only when lumbar puncture can be safely performed, radiology (MRI brain, CT CAP), will help to support the diagnosis of PCNSL. Stereotactic brain biopsy is the only confirmatory test and this may be guided by gadolinium-enhanced MRI scan. The presence of Epstein–Barr virus (EBV) in tumour cells is a universal SB431542 order feature of HIV-associated PCNSL but is not found in other PCNSLs [5,6]. In patients with HIV, computed tomography (CT) scans of PCNSL may show ring enhancement in as many

as half the cases, whilst in immunocompetent patients with PCNSL the enhancement is almost Chlormezanone always homogeneous [7,8]. Most commonly, PCNSL presents as diffuse and multifocal supratentorial brain masses. As a peculiarity of PCNSL, involvement of the vitreous, retina and optic nerves may be found in about 10–15% of patients at presentation [9]. Lymphomatous infiltration of the leptomeninges or ependymal surfaces and radicular or plexus invasion may occur as well [10]. By systemic staging, occult systemic lymphoma may be detected in up to

8% of patients initially presenting with brain lymphoma. Therefore, bone marrow biopsy, CT scan of chest and abdomen, testicular ultrasound and careful physical examination to detect occult systemic lymphoma is recommended [11]. The diagnostic algorithm for the management of cerebral mass lesions in HIV-seropositive patients includes a 2-week trial of antitoxoplasmosis therapy (sulfadiazine 1 g four times a day, pyrimethamine 75 mg once daily). Magnetic resonance imaging is the most sensitive radiological procedure: the densely cellular tumour appears as single (65%) or multiple lesions on nonenhanced T1-weighted images, hyperintense tumour and oedema on T2 or FLAIR images and densely enhancing masses after administration of gadolinium. Fifty per cent or more of the lesions are in contact with the meninges, and meningeal enhancement appears in 10–20% [12]. The treatment of HIV-associated primary cerebral lymphoma is poor with median survival rarely reported at greater than 9 months.