Documento descargado de http://www.elsevier.es el 17/11/2016. Copia para uso personal, se prohíbe la transmisión de este documento por cualquier medio o formato. Rev Esp Med Nucl Imagen Mol. 2014;33(1):50–51 Interesting images Neurolymphomatosis as initial manifestation of recurrence in lymphoma夽 Neurolinfomatosis como manifestación inicial de recidiva en linfoma D. Ramírez Ocaña a,∗ , A.L. Gutiérrez Cardo b , L. González Díaz c , K. Hurst c , M. Espeso de Haro c a b c Unidad de Gestión Clínica de Medicina Nuclear, Hospital Universitario Carlos Haya, Málaga, Spain Unidad de Imagen Molecular, Centro de Investigaciones Médico Sanitarias, Málaga, Spain Unidad de Gestión Clínica de Hematología y Hemoterapia, Hospital Universitario Carlos Haya, Málaga, Spain a r t i c l e i n f o Article history: Received 11 December 2012 Accepted 12 February 2013 We present the case of a 71-year-old woman diagnosed with diffuse large B-cell non-Hodgkin lymphoma, stage IV-B, IPI 3, in complete remission after 6 cycles of rituximab-CHOP. Five months after completing treatment the patient went to the Emergency Department for a picture of headache and diplopy of one month of evolution. During admission she present lumbosciatalgia refractory to pharmacologic treatment. Lumbosacral MR was performed showing no signs of lymphomatous disease (Fig. 1). CSF study demonstrated relapse of lymphoma in the CNS and intrathecal therapy was initiated. At the end of the treatment 18 FFDG/PET-CT showed hypermetabolic foci in axillary, lumbar and pelvis regions compatible with nervous system tumoral involvement (neurolymphomatosis). In addition, hypermetabolic foci in the humeral head and sacrum were observed compatible with bone involvement by lymphoma (Fig. 2). Lymphatic infiltration of the peripheral nervous system (neurolymphomatosis) is a rare manifestation of non-Hodgkin lymphoma. It is usually presented in patients with very extended non-Hodgkin lymphoma or as the first manifestation of relapse.1 The onset of symptoms is generally progressive and insidious, presenting only radicular pain or associated to central or peripheral sensitivo-motor neuropathy. Pain is the most common clinical presentation, generally being intense and described as relentless and, sometimes, burning pain. Neuropathy may present clinical symptoms similar to the Guillain-Barré syndrome, cauda equina syndrome (horse-tail) or quadriparesia, and differential diagnosis should include chemotherapy-induced neurotoxicity, infections, compression of a nerve root, radicular neuropathy and vasculitis.2 Definitive diagnosis requires histological confirmation of the affected nerve, which, on occasions cannot be performed and is often not diagnostic since the affected zone may not be accessible to biopsy. Fig. 1. Sagittal T2-weighted sequence MR images of the lumbosacral spine showing multiple degenerative changes with no evidence of lymphomatous disease. 夽 Please cite this article as: Ramírez Ocaña D, Gutiérrez Cardo AL, González Díaz L, Hurst K, Espeso de Haro M. Neurolinfomatosis como manifestación inicial de recidiva en linfoma. Rev Esp Med Nucl Imagen Mol. 2014;33:50–51. ∗ Corresponding author. E-mail address: d [email protected] (D. Ramírez Ocaña). 2253-8089/$ – see front matter © 2012 Elsevier España, S.L. and SEMNIM. All rights reserved. Documento descargado de http://www.elsevier.es el 17/11/2016. Copia para uso personal, se prohíbe la transmisión de este documento por cualquier medio o formato. D. Ramírez Ocaña et al. / Rev Esp Med Nucl Imagen Mol. 2014;33(1):50–51 51 Fig. 2. 18 F-FDG/PET-CT study: (a) MIP showing an increase in the 18 F-FDG uptake in the left humeral head, sacrum and axillary and lumbar plexus. (b) PET, (c) CT and (d) fusion 18 F-FDG/PET-CT coronal images showing lineal uptake corresponding with the left lumbar plexus suggestive of infiltration by lymphoma. Fig. 3. Axial 18 F-FDG/PET-CT images showing an increase in the 18 F-FDG uptake in the right brachial plexus suggestive of lymphomatous infiltration. MR is the imaging test presenting the best performance for the study of metastasis of the plexus and may show a slight mass adjacent to the plexus or identify metastatic infiltration. However, none of these characteristics is specific and, in some circumstances, the MR may be normal. 18 F-FDG/PET-CT plays an essential role in staging, in the evaluation of response to treatment and in the detection of recurrence of lymphoma. Since the study assesses the entire whole body, it allows the restaging of the disease and the identification of tumor dissemination patterns which may be atypical.3 The use of hybrid images achieves precise localization (Fig. 3) and allows guidance of the biopsy to more accessible sites with greater metabolic activity in an attempt to reduce the rate of false negative results. In our case, 18 F-FDG/PET-CT confirmed the presence of tumor recurrence, demonstrating an increase in the uptake in the nervous structures which, together with the symptomatology referred, allowed the diagnostic suspicion of neurolymphomatosis and identified the site for performing the biopsy. Conflict of interest The authors have no conflicts of interest to declare. References 1. Even-Sapir E, Lievshitz G, Perry C, Herishanu Y, Lerman H, Metser U. Fluorine18 fluorodeoxyglucose PET/CT patterns of extranodal involvement in patients with Non-Hodgkin lymphoma and Hodgkin’s disease. Radiol Clin North Am. 2007;45:697–709. 2. Kanter P, Zeidman A, Streifler J, Marmelstein V, Even-Sapir E, Metser U, et al. PETCT imaging of combined brachial and lumbosacral neurolymphomatosis. Eur J Haematol. 2005;74:66–9. 3. Alvarez Páez AM, Nogueiras Alonso JM, Serena Puig A. 18F-FDG-PET/CT in lymphoma: two decades of experience. Rev Esp Med Nucl Imagen Mol. 2012;31:340–9.