We report a case of a 71-year-old Caucasian female who presented with two to three weeks of horizontal diplopia and coordination difficulty in the right upper extremity. She also reported weight loss and a low grade fever. Patient had a medical history of hypertension, hyperlipidemia, hypothyroidism, and anxiety and a family history of hypertension only. Patient reported she was a former smoker of 4-5 cigarettes a day for 2-3 years in her 20s, drinks alcohol socially, and has never participated in illicit drug use.Her physical finding of note included right homonymous upper quadrantanopia, binocular diplopia evident upon looking to the left, normal other cranial nerves, right upper extremity strength of graded 5/5-proximally and 4+/5 distally, right upper extremity past pointing and subtle ataxia on the right, including finger to nose and the heel to shin test, as well as gait ataxia.MRI of the brain was performed with and without contrast and showed multiple hyper-intense lesions involving the basal ganglion, thalamus, midbrain, pons, temporal lobe, occipital lobe, and enhancing corpus callosal lesions. There was no evidence of edema, necrosis, or ring enhancement, as shown in Figure 1. Lesions were found to cross the midline via the corpus callosum.The differential diagnosis included neoplasms, demyelinating disorders and autoimmune and inflammatory conditions, infections, vascular causes, and trauma, which are discussed below along with representative MRI images.
AbstractPrimary Central Nervous System Lymphoma (PCNSL) is a rare non-Hodgkin type neoplasm, which crosses the midline. We report an unusual case of a 71-year-old Caucasian female who was shown to have PCNSL by a tissue biopsy after the brain Magnetic Resonance Imaging (MRI) showed Central Nervous System (CNS) lesions crossing the corpus callosum. We propose that PCNSL should be considered in the differential diagnosis of midline crossing lesions. Awareness of this is imperative for treatment decisions for such patients.