Peripheral nervous system involvement in lymphomas
Corresponding Author
Chiara Briani
Department of Neuroscience, University of Padova, Padova, Italy
Correspondence
Chiara Briani, MD, Department of Neurosciences, University of Padova, Via Giustiniani, 5, 35128 Padova, Italy.
Email: [email protected]
Search for more papers by this authorAndrea Visentin
Hematology and Clinical Immunology Unit, Department of Medicine, University of Padova, Padova, Italy
Search for more papers by this authorMarta Campagnolo
Department of Neuroscience, University of Padova, Padova, Italy
Search for more papers by this authorAlessandro Salvalaggio
Department of Neuroscience, University of Padova, Padova, Italy
Search for more papers by this authorSergio Ferrari
Department of Neurology, Azienda Ospedaliera Universitaria Integrata, University Hospital G.B. Rossi, Verona, Italy
Search for more papers by this authorTiziana Cavallaro
Department of Neurology, Azienda Ospedaliera Universitaria Integrata, University Hospital G.B. Rossi, Verona, Italy
Search for more papers by this authorRenzo Manara
Neuroradiology, Department of Medicine and Surgery, University of Salerno, Fisciano, Italy
Search for more papers by this authorRoberto Gasparotti
Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, Brescia, Italy
Search for more papers by this authorFrancesco Piazza
Hematology and Clinical Immunology Unit, Department of Medicine, University of Padova, Padova, Italy
Search for more papers by this authorCorresponding Author
Chiara Briani
Department of Neuroscience, University of Padova, Padova, Italy
Correspondence
Chiara Briani, MD, Department of Neurosciences, University of Padova, Via Giustiniani, 5, 35128 Padova, Italy.
Email: [email protected]
Search for more papers by this authorAndrea Visentin
Hematology and Clinical Immunology Unit, Department of Medicine, University of Padova, Padova, Italy
Search for more papers by this authorMarta Campagnolo
Department of Neuroscience, University of Padova, Padova, Italy
Search for more papers by this authorAlessandro Salvalaggio
Department of Neuroscience, University of Padova, Padova, Italy
Search for more papers by this authorSergio Ferrari
Department of Neurology, Azienda Ospedaliera Universitaria Integrata, University Hospital G.B. Rossi, Verona, Italy
Search for more papers by this authorTiziana Cavallaro
Department of Neurology, Azienda Ospedaliera Universitaria Integrata, University Hospital G.B. Rossi, Verona, Italy
Search for more papers by this authorRenzo Manara
Neuroradiology, Department of Medicine and Surgery, University of Salerno, Fisciano, Italy
Search for more papers by this authorRoberto Gasparotti
Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, Brescia, Italy
Search for more papers by this authorFrancesco Piazza
Hematology and Clinical Immunology Unit, Department of Medicine, University of Padova, Padova, Italy
Search for more papers by this authorAbstract
The peripheral nervous system may be involved at any stage in the course of lymphoproliferative diseases. The different underlying mechanisms include neurotoxicity secondary to chemotherapy, direct nerve infiltration (neurolymphomatosis), infections, immune-mediated, paraneoplastic or metabolic processes and nutritional deficiencies. Accordingly, the clinical features are heterogeneous and depend on the localization of the damage (ganglia, roots, plexi, and peripheral nerves) and on the involved structures (myelin, axon, and cell body). Some clinical findings, such a focal or diffuse involvement, symmetric or asymmetric pattern, presence of pain may point to the correct diagnosis. Besides a thorough medical history and neurological examination, neurophysiological studies, cerebrospinal fluid analysis, nerve biopsy (in selected patients with suspected lymphomatous infiltration) and neuroimaging techniques (magnetic resonance neurography and nerve ultrasound) may be crucial for a proper diagnostic workup.
REFERENCES
- 1Swerdlow SH, Campo E, Pileri SA, et al. The 2016 revision of the World Health Organization classification of lymphoid neoplasms. Blood. 2016; 127: 2375-2390.
- 2Kelly JJ, Karcher DS. Lymphoma and peripheral neuropathy: a clinical review. Muscle Nerve. 2005; 31: 301-313.
- 3Odabasi Z, Parrott JH, Reddy VV, Oh SJ. Neurolymphomatosis associated with muscle and cerebral involvement caused by natural killer cell lymphoma: a case report and review of literature. J Peripher Nerv Syst. 2001; 6: 197-203.
- 4Richelli S, Buono R, Ferrari S, Vattemi G, Monaco S. Acute inflammatory demyelinating polyneuropathy as a manifestation of chronic lymphoproliferative disorder of NK cells. Neurol Sci. 2015; 36: 1041-1043.
- 5Brahmer JR, Lacchetti C, Schneider BJ, et al. Management of immune-related adverse events in patients treated with immune checkpoint inhibitor therapy: American Society of Clinical Oncology clinical practice guideline. J Clin Oncol. 2018; 36: 1714-1768.
- 6Dalakas MC. Neurological complications of immune checkpoint inhibitors: what happens when you ‘take the brakes off’ the immune system. Ther Adv Neurol Disord. 2018; 11:1-12.
- 7Viala K, Behin A, Maisonobe T, et al. Neuropathy in lymphoma: a relationship between the pattern of neuropathy, type of lymphoma and prognosis? J Neurol Neurosurg Psychiatry. 2008; 79: 778-782.
- 8Hughes RA, Britton T, Richards M. Effects of lymphoma on the peripheral nervous system. J R Soc Med. 1994; 87: 526-530.
- 9Lisak RP, Mitchell M, Zweiman B, Orrechio E, Asbury AK. Guillain-Barre syndrome and Hodgkin's disease: three cases with immunological studies. Ann Neurol. 1977; 1: 72-78.
- 10Briani C, Vitaliani R, Grisold W, et al. Spectrum of paraneoplastic disease associated with lymphoma. Neurology. 2011; 76: 705-710.
- 11Stubgen JP. Lymphoma-associated dysimmune polyneuropathies. J Neurol Sci. 2015; 355: 25-36.
- 12Hallek M, Shanafelt TD, Eichhorst B. Chronic lymphocytic leukaemia. Lancet. 2018; 391: 1524-1537.
- 13Visentin A, Imbergamo S, Gurrieri C, et al. Major infections, secondary cancers and autoimmune diseases occur in different clinical subsets of chronic lymphocytic leukaemia patients. Eur J Cancer. 2017; 72: 103-111.
- 14Visentin A, Facco M, Frezzato F, et al. Integrated CLL scoring system, a new and simple index to predict time to treatment and overall survival in patients with chronic lymphocytic leukemia. Clin Lymphoma Myeloma Leuk. 2015; 15(612–620): e611-e615.
- 15Briani C, Visentin A, Cavallaro T, et al. Primary neurolymphomatosis as clinical onset of chronic lymphocytic leukemia. Ann Hematol. 2017a; 96: 159-161.
- 16Briani C, Visentin A, Salvalaggio A, et al. Peripheral neuropathies in chronic lymphocytic leukemia: a single center experience on 816 patients. Haematologica. 2017b; 102: e140-e143.
- 17Visentin A, Briani C, Imbergamo S, et al. Idelalisib plus rituximab is effective in systemic AL amyloidosis secondary to chronic lymphocytic leukaemia. Hematol Oncol. 2018; 36: 366-369.
- 18Van den Bergh PY, Hadden RD, Bouche P, et al. European Federation of Neurological S, Peripheral Nerve SEuropean Federation of Neurological Societies/Peripheral Nerve Society guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society - first revision. Eur J Neurol. 2010; 17: 356-363.
- 19Briani C, Visentin A, Salvalaggio A, Cacciavillani M, Trentin L. Obinutuzumab, a new anti-CD20 antibody, and chlorambucil are active and effective in anti-MAG antibody polyneuropathy. Eur J Neurol. 2018. https://doi.org/10.1111/ene.13838. [Epub ahead of print].
- 20Castillo JJ, Treon SP. Initial evaluation of the patient with Waldenstrom Macroglobulinemia. Hematol Oncol Clin North Am. 2018; 32: 811-820.
- 21Treon SP, Xu L, Liu X, Hunter ZR, Yang G, Castillo JJ. Genomic landscape of Waldenstrom Macroglobulinemia. Hematol Oncol Clin North Am. 2018; 32: 745-752.
- 22Boso F, Ruggero S, Giannotta C, et al. Anti-sulfatide/galactocerebroside antibodies in immunoglobulin M paraproteinemic neuropathies. Eur J Neurol. 2017; 24: 1334-1340.
- 23Campagnolo M, Ferrari S, Dalla Torre C, et al. Polyneuropathy with anti-sulfatide and anti-MAG antibodies: clinical, neurophysiological, pathological features and response to treatment. J Neuroimmunol. 2015; 281: 1-4.
- 24Rajabally YA. Neuropathy and paraproteins: review of a complex association. Eur J Neurol. 2011; 18: 1291-1298.
- 25Willison HJ, O'Leary CP, Veitch J, et al. The clinical and laboratory features of chronic sensory ataxic neuropathy with anti-disialosyl IgM antibodies. Brain. 2001; 124: 1968-1977.
- 26Muchtar E, Magen H, Gertz MA. How I treat cryoglobulinemia. Blood. 2017; 129: 289-298.
- 27Rosenbaum E, Marks D, Raza S. Diagnosis and management of neuropathies associated with plasma cell dyscrasias. Hematol Oncol. 2018; 36: 3-14.
- 28Latov N. Diagnosis and treatment of chronic acquired demyelinating polyneuropathies. Nat Rev Neurol. 2014; 10: 435-446.
- 29Lunn MP, Nobile-Orazio E. Immunotherapy for IgM anti-myelin-associated glycoprotein paraprotein-associated peripheral neuropathies. Cochrane Database Syst Rev. 2016; 10: CD002827.
- 30Dalakas MC. Advances in the diagnosis, immunopathogenesis and therapies of IgM-anti-MAG antibody-mediated neuropathies. Ther Adv Neurol Disord. 2018 11:1756285617746640.
- 31Campagnolo M, Zambello R, Nobile-Orazio E, et al. IgM MGUS and Waldenstrom-associated anti-MAG neuropathies display similar response to rituximab therapy. J Neurol Neurosurg Psychiatry. 2017; 88: 1094-1097.
- 32Treon SP, Xu L, Hunter Z. MYD88 mutations and response to Ibrutinib in Waldenstrom's Macroglobulinemia. N Engl J Med. 2015; 373: 584-586.
- 33Milani P, Merlini G. Monoclonal IgM-related AL amyloidosis. Best Pract Res Clin Haematol. 2016; 29: 241-248.
- 34Lenz G, Staudt LM. Aggressive lymphomas. N Engl J Med. 2010; 362: 1417-1429.
- 35Wright GW, Wilson WH, Staudt LM. Genetics of diffuse large B-cell lymphoma. N Engl J Med. 2018; 379: 493-494.
- 36Tomita M, Koike H, Kawagashira Y, et al. Clinicopathological features of neuropathy associated with lymphoma. Brain. 2013; 136: 2563-2578.
- 37Del Grande A, Sabatelli M, Luigetti M, et al. Primary multifocal lymphoma of peripheral nervous system: case report and review of the literature. Muscle Nerve. 2014; 50: 1016-1022.
- 38He W, Wang W, Gustas C, Malysz J, Kaur D. Isolated sciatic neuropathy as an initial manifestation of a high grade B-cell lymphoma: a case report and literature review. Clin Neurol Neurosurg. 2016; 149: 147-153.
- 39Liu AY, Nabel CS, Finkelman BS, et al. Idiopathic multicentric Castleman's disease: a systematic literature review. Lancet Haematol. 2016; 3: e163-e175.
- 40Scarlato M, Previtali SC, Carpo M, et al. Polyneuropathy in POEMS syndrome: role of angiogenic factors in the pathogenesis. Brain. 2005; 128: 1911-1920.
- 41Naddaf E, Dispenzieri A, Mandrekar J, Mauermann ML. Clinical spectrum of Castleman disease-associated neuropathy. Neurology. 2016; 87: 2457-2462.
- 42van Rhee F, Greenway A, Stone K. Treatment of idiopathic Castleman disease. Hematol Oncol Clin North Am. 2018; 32: 89-106.
- 43van Rhee F, Wong RS, Munshi N, et al. Siltuximab for multicentric Castleman's disease: a randomised, double-blind, placebo-controlled trial. Lancet Oncol. 2014; 15: 966-974.
- 44Wrotnowski U, Mills SE, Cooper PH. Malignant angioendotheliomatosis. An angiotropic lymphoma? Am J Clin Pathol. 1985; 83: 244-248.
- 45Ponzoni M, Campo E, Nakamura S. Intravascular large B-cell lymphoma: a chamaleon with multiple faces and many masks. Blood. 2018;132(15):1561-1567. https://doi.org/10.1182/blood-2017-04-737445.
- 46Ponzoni M, Ferreri AJ. Intravascular lymphoma: a neoplasm of 'homeless' lymphocytes? Hematol Oncol. 2006; 24: 105-112.
- 47Jiang QL, Pytel P, Rowin J. Disseminated intravascular large-cell lymphoma with initial presentation mimicking Guillain-Barre syndrome. Muscle Nerve. 2010; 42: 133-136.
- 48Lynch KM, Katz JD, Weinberg DH, Lin DI, Folkerth RD. Isolated mononeuropathy multiplex--a rare manifestation of intravascular large B-cell lymphoma. J Clin Neuromuscul Dis. 2012; 14: 17-20.
- 49Darnell RB, Posner JB. Paraneoplastic syndromes affecting the nervous system. Semin Oncol. 2006; 33: 270-298.
- 50Giometto B, Grisold W, Vitaliani R, et al. Paraneoplastic neurologic syndrome in the PNS Euronetwork database: a European study from 20 centers. Arch Neurol. 2010; 67: 330-335.
- 51Graus F, Arino H, Dalmau J. Paraneoplastic neurological syndromes in Hodgkin and non-Hodgkin lymphomas. Blood. 2014; 123: 3230-3238.
- 52Flanagan EP, Sandroni P, Pittock SJ, Inwards DJ, Jones LK Jr. Paraneoplastic lower motor neuronopathy associated with Hodgkin lymphoma. Muscle Nerve. 2012; 46: 823-827.
- 53Schold SC, Cho ES, Somasundaram M, Posner JB. Subacute motor neuronopathy: a remote effect of lymphoma. Ann Neurol. 1979; 5: 271-287.
- 54Baehring JM, Damek D, Martin EC, Betensky RA, Hochberg FH. Neurolymphomatosis. Neuro-Oncology. 2003; 5: 104-115.
- 55Lhermitte J, Trelles J. Neurolymphomatose périphérique humaine. Presse Med. 1934; 42: 289-292.
- 56Avila J, Vivar C. Neurolymphomatosis: a review of 82 cases (P5.141). Neurology. 2017; 88(suppl 16).
- 57Zimmermann H. Malignant lymphomas of the nervous system. Acta Neuropathol. 1975;6: 69-74.
- 58Kern WF, Spier CM, Hanneman EH, Miller TP, Matzner M, Grogan TM. Neural cell adhesion molecule-positive peripheral T-cell lymphoma: a rare variant with a propensity for unusual sites of involvement. Blood. 1992; 79: 2432-2437.
- 59Meller I, Alkalay D, Mozes M, Geffen DB, Ferit T. Isolated metastases to peripheral nerves. Report of five cases involving the brachial plexus. Cancer. 1995; 76: 1829-1832.
10.1002/1097-0142(19951115)76:10<1829::AID-CNCR2820761023>3.0.CO;2-7 CAS PubMed Web of Science® Google Scholar
- 60Baehring JM, Batchelor TT. Diagnosis and management of neurolymphomatosis. Cancer J. 2012; 18: 463-468.
- 61Grisariu S, Avni B, Batchelor TT, et al. International Primary CNSLCGNeurolymphomatosis: an international primary CNS lymphoma collaborative group report. Blood. 2010; 115: 5005-5011.
- 62Kamiya-Matsuoka C, Shroff S, Gildersleeve K, Hormozdi B, Manning JT, Woodman KH. Neurolymphomatosis: a case series of clinical manifestations, treatments, and outcomes. J Neurol Sci. 2014; 343: 144-148.
- 63van den Bent MJ, de Bruin HG, Beun GD, Vecht CJ. Neurolymphomatosis of the median nerve. Neurology. 1995; 45: 1403-1405.
- 64Gordon PH, Younger DS. Neurolymphomatosis. Neurology. 1996; 46: 1191-1192.
- 65Moore KR, Blumenthal DT, Smith AG, Ward JH. Neurolymphomatosis of the lumbar plexus: high-resolution MR neurography findings. Neurology. 2001; 57: 740-742.
- 66Strobel K, Fischer K, Hany TF, Poryazova R, Jung HH. Sciatic nerve neurolymphomatosis - extent and therapy response assessment with PET/CT. Clin Nucl Med. 2007; 32: 646-648.
- 67Trojan A, Jermann M, Taverna C, Hany TF. Fusion PET-CT imaging of neurolymphomatosis. Ann Oncol. 2002; 13: 802-805.
- 68Kim JH, Jang JH, Koh SB. A case of neurolymphomatosis involving cranial nerves: MRI and fusion PET-CT findings. J Neuro-Oncol. 2006; 80: 209-210.
- 69Bokstein F, Goor O, Shihman B, et al. Assessment of neurolymphomatosis by brachial plexus biopsy and PET/CT. Report of a case. J Neuro-Oncol. 2005; 72: 163-167.
- 70Kanter P, Zeidman A, Streifler J, et al. PET-CT imaging of combined brachial and lumbosacral neurolymphomatosis. Eur J Haematol. 2005; 74: 66-69.
- 71Kinoshita H, Yamakado H, Kitano T, et al. Diagnostic utility of FDG-PET in neurolymphomatosis: report of five cases. J Neurol. 2016; 263: 1719-1726.
- 72Choi AL, Koh SH, Jun SY, et al. Lymphoma involving the ulnar nerve: sonographic findings. J Ultrasound Med. 2008; 27: 1527-1531.
- 73Vijayan J, Chan YC, Therimadasamy A, Wilder-Smith EP. Role of combined B-mode and Doppler sonography in evaluating neurolymphomatosis. Neurology. 2015; 85: 752-755.
- 74Diaz-Arrastia R, Younger DS, Hair L, et al. Neurolymphomatosis: a clinicopathologic syndrome re-emerges. Neurology. 1992; 42: 1136-1141.
- 75Thomas FP, Vallejos U, Foitl DR, et al. B cell small lymphocytic lymphoma and chronic lymphocytic leukemia with peripheral neuropathy: two cases with neuropathological findings and lymphocyte marker analysis. Acta Neuropathol. 1990; 80: 198-203.
- 76Purohit DP, Dick DJ, Perry RH, Lyons PR, Schofield IS, Foster JB. Solitary extranodal lymphoma of sciatic nerve. J Neurol Sci. 1986; 74: 23-34.
- 77Briani C, Zambello R, Cavallaro T, et al. Improvement of peripheral nervous system manifestations of B-cell non-Hodgkin's lymphoma after rituximab therapy. J Peripher Nerv Syst. 2009; 14: 146-148.
- 78Ferreri AJ, Cwynarski K, Pulczynski E, et al. International Extranodal lymphoma study group (IELSG)Chemoimmunotherapy with methotrexate, cytarabine, thiotepa, and rituximab (MATRix regimen) in patients with primary CNS lymphoma: results of the first randomisation of the international Extranodal lymphoma study Group-32 (IELSG32) phase 2 trial. Lancet Haematol. 2016; 3: 217-227.
- 79Grimm S, Chamberlain M. Hodgkin's lymphoma: a review of neurologic complications. Adv Hematol. 2011; 2011: 624578.
- 80Stubblefield MD. Neuromuscular complications of radiation therapy. Muscle Nerve. 2017; 56: 1031-1040.
- 81Rowin J, Cheng G, Lewis SL, Meriggioli MN. Late appearance of dropped head syndrome after radiotherapy for Hodgkin's disease. Muscle Nerve. 2006; 34: 666-669.
- 82Shibuya K, Misawa S, Hirano S, Kuwabara S. Acute brachial plexopathy caused by Burkitt's lymphoma infiltration. Intern Med. 2013; 52: 931.
- 83Bourque PR, Warman Chardon J, Bryanton M, Toupin M, Burns BF, Torres C. Neurolymphomatosis of the brachial plexus and its branches: case series and literature review. Can J Neurol Sci. 2018; 45: 137-143.
- 84Gwathmey KG. Plexus and peripheral nerve metastasis. Handb Clin Neurol. 2018; 149: 257-279.
- 85Lederman RJ, Wilbourn AJ. Brachial plexopathy: recurrent cancer or radiation? Neurology. 1984;34:1331-1335.
- 86Ruiz E, Resende LS, Gaiolla RD, Niéro-Melo L, Custódio Domingues MA, de Lima Resende LA. Post-Ganglionic Horner's syndrome: an unusual presentation of non-Hodgkin lymphoma. Case Rep Neurol. 2012; 4: 43-46.
- 87Cai Z, Li Y, Hu Z, et al. Radiation-induced brachial plexopathy in patients with nasopharyngeal carcinoma: a retrospective study. Oncotarget. 2016; 7: 18887-18895.
- 88Gasparotti R, Padua L, Briani C, Lauria G. New technologies for the assessment of neuropathies. Nat Rev Neurol. 2017; 13: 203-216.
- 89Andreou A, Sohaib A, Collins DJ, et al. Diffusion-weighted MR neurography for the assessment of brachial plexopathy in oncological practice. Cancer Imaging. 2015; 15: 6.
- 90Ho L, Henderson R, Luong T, Malkhassian S, Wassef H. 18F-FDG PET/CT appearance of metastatic brachial plexopathy involving epidural space from breast carcinoma. Clin Nucl Med. 2012; 37: e263-e264.
- 91Cacciavillani M, Salvalaggio A, Ruiz M, Briani C. Ultrasound in the evaluation of neuromuscular complications of radiation therapy. Muscle Nerve. 2018; 57: E104-E105.
- 92Hansson E, Forbes HJ, Langan SM, Smeeth L, Bhaskaran K. Herpes zoster risk after 21 specific cancers: population-based case-control study. Br J Cancer. 2017; 116: 1643-1651.
- 93Aksoy S, Harputluoglu H, Kilickap S, et al. Rituximab-related viral infections in lymphoma patients. Leuk Lymphoma. 2007; 48: 1307-1312.
- 94Cho SF, Wu WH, Yang YH, Liu YC, Hsiao HH, Chang CS. Longitudinal risk of herpes zoster in patients with non-Hodgkin lymphoma receiving chemotherapy: a nationwide population-based study. Sci Rep. 2015; 5: 14008.
- 95Salvalaggio A, Cacciavillani M, Visentin A, Campagnolo M, Trentin L, Briani C. Nerve ultrasound abnormalities mirror the course of varicella zoster virus sensory-motor radiculoplexopathy. Muscle Nerve. 2017; 55: E16-E18.
- 96Grisold W, Briani C, Vass A. Malignant cell infiltration in the peripheral nervous system. Handb Clin Neurol. 2013; 115: 685-712.
- 97Hegde U, Filie A, Little RF, et al. High incidence of occult leptomeningeal disease detected by flow cytometry in newly diagnosed aggressive B-cell lymphomas at risk for central nervous system involvement: the role of flow cytometry versus cytology. Blood. 2005; 105: 496-502.
- 98Massa A, Fozza C. Large B-cell non Hodgkin lymphoma relapsing with meningeal localization. Blood. 2012; 119: 6185.
- 99Morita M, Osawa M, Naruse H, Nakamura H. Primary NK/T-cell lymphoma of the cauda equina: a case report and literature review. Spine (Phila Pa 1976). 2009; 34: E882-E885.
- 100Tahiri L, Benbouazza K, Amine B, Allali F, El Mesbahi O, Hajjaj-Hassouni N. Primary non-Hodgkin's lymphoma presenting as radicular syndrome: report of two cases. Rheumatol Int. 2009; 30: 113-117.
- 101Grisold W, Klimpfinger M, Maehr B, et al. Peripheral nerve involvement in lymphoma: the meninges as the crucial barrier between meningoradicular spread and neurolymphomatosis. J Peripher Nerv Syst. 2007; 12: 58-60.
- 102Binda D, Cavaletti G, Cornblath DR, Merkies IS. group CI-PsRasch-transformed total neuropathy score clinical version (RT-TNSc([c])) in patients with chemotherapy-induced peripheral neuropathy. J Peripher Nerv Syst. 2015; 20: 328-332.
- 103Cavaletti G, Marmiroli P. Chemotherapy-induced peripheral neurotoxicity. Curr Opin Neurol. 2015; 28: 500-507.
- 104Magge RS, DeAngelis LM. The double-edged sword: neurotoxicity of chemotherapy. Blood Rev. 2015; 29: 93-100.
- 105Stone JB, DeAngelis LM. Cancer-treatment-induced neurotoxicity--focus on newer treatments. Nat Rev Clin Oncol. 2016; 13: 92-105.
- 106van de Velde ME, Kaspers GL, Abbink FCH, Wilhelm AJ, Ket JCF, van den Berg MH. Vincristine-induced peripheral neuropathy in children with cancer: a systematic review. Crit Rev Oncol Hematol. 2017; 114: 114-130.
- 107Egbelakin A, Ferguson MJ, MacGill EA, et al. Increased risk of vincristine neurotoxicity associated with low CYP3A5 expression genotype in children with acute lymphoblastic leukemia. Pediatr Blood Cancer. 2011; 56: 361-367.
- 108Kandula T, Park SB, Cohn RJ, Krishnan AV, Farrar MA. Pediatric chemotherapy induced peripheral neuropathy: a systematic review of current knowledge. Cancer Treat Rev. 2016; 50: 118-128.
- 109Cil T, Altintas A, Tamam Y, Battaloglu E, Isikdogan A. Low dose vincristine-induced severe polyneuropathy in a Hodgkin lymphoma patient: a case report (vincristine-induced severe polyneuropathy). J Pediatr Hematol Oncol. 2009; 31: 787-789.
- 110Hildebrandt G, Holler E, Woenkhaus M, et al. Acute deterioration of Charcot-Marie-Tooth disease IA (CMT IA) following 2 mg of vincristine chemotherapy. Ann Oncol. 2000; 11: 743-747.
- 111Nakamura T, Hashiguchi A, Suzuki S, Uozumi K, Tokunaga S, Takashima H. Vincristine exacerbates asymptomatic Charcot-Marie-Tooth disease with a novel EGR2 mutation. Neurogenetics. 2012; 13: 77-82.
- 112Trobaugh-Lotrario AD, Smith AA, Odom LF. Vincristine neurotoxicity in the presence of hereditary neuropathy. Med Pediatr Oncol. 2003; 40: 39-43.
- 113Marmiroli P, Scuteri A, Cornblath DR, Cavaletti G. Pain in chemotherapy-induced peripheral neurotoxicity. J Peripher Nerv Syst. 2017; 22: 156-161.
- 114Richardson PG, Briemberg H, Jagannath S, et al. Frequency, characteristics, and reversibility of peripheral neuropathy during treatment of advanced multiple myeloma with bortezomib. J Clin Oncol. 2006; 24: 3113-3120.
- 115Richardson PG, Sonneveld P, Schuster MW, et al. Reversibility of symptomatic peripheral neuropathy with bortezomib in phase III APEX trial in relapsed multiple myeloma: impact of a dose-modification guideline. Br J Hematol. 2009; 144: 895-903.
- 116Dimopoulos MA, Mateos MV, Richardson PG, et al. Risk factors for, and reversibility of, peripheral neuropathy associated with bortezomib-melphalan-prednisone in newly diagnosed patients with multiple myeloma: subanalysis of the phase 3 VISTA study. Eur J Haematol. 2011; 86: 23-31.
- 117Cioroiu C, Weimer LH. Update on chemotherapy-induced peripheral neuropathy. Curr Neurol Neurosci Rep. 2017; 17: 47.
- 118Mu SD, Ai LS, Qin Y, Hu Y. Subcutaneous versus intravenous bortezomib administration for multiple myeloma patients: a meta-analysis. Curr Med Sci. 2018; 38: 43-50.
- 119Mushtaq A, Kapoor V, Latif A, et al. Efficacy and toxicity profile of carfilzomib based regimens for treatment of multiple myeloma: a systematic review. Crit Rev Oncol Hematol. 2018; 125: 1-11.
- 120Dalla Torre C, Zambello R, Cacciavillani M, et al. Lenalidomide long-term neurotoxicity: clinical and neurophysiologic prospective study. Neurology. 2016; 87: 1161-1166.
- 121Nozza A, Terenghi F, Gallia F, et al. Lenalidomide and dexamethasone in patients with POEMS syndrome: results of a prospective, open-label trial. Br J Haematol. 2017; 179: 748-755.
- 122Mariotto S, Ferrari S, Monaco S. Brentuximab vedotin-induced peripheral neuropathy: looking at microtubules. J Neuro-Oncol. 2018a; 137: 665-666.
- 123Pastorelli F, Derenzini E, Plasmati R, et al. Severe peripheral motor neuropathy in a patient with Hodgkin lymphoma treated with brentuximab vedotin. Leuk Lymphoma. 2013; 54: 2318-2321.
- 124Corbin ZA, Nguyen-Lin A, Li S, et al. Characterization of the peripheral neuropathy associated with brentuximab vedotin treatment of Mycosis Fungoides and Sezary Syndrome. J Neuro-Oncol. 2017; 132: 439-446.
- 125Barp A, Gilardin L, Afanasiev V, et al. Subacute inflammatory demyelinating polyradiculoneuropathy complicating relapsing Hodgkin lymphoma: another immune-related adverse event of the anti-PD1 therapy? Leuk Lymphoma. 2018; 1-3.
- 126Alberti P, Parma M, Pioltelli P, et al. Severe, reversible nelarabine-induced neuropathy and myelopathy. J Peripher Nerv Syst. 2016; 21: 154-156.
- 127Lalayanni C, Baldoumi E, Papayiannopoulos S, Tziola K, Saloum R, Anagnostopoulos A. Nelarabine-associated reversible Guillain-Barre-like syndrome or myelopathy in an adult patient with primary refractory T-lymphoblastic lymphoma. Curr Probl Cancer. 2017; 41: 138-143.
- 128Grauer O, Wolff D, Bertz H, et al. Neurological manifestations of chronic graft-versus-host disease after allogeneic haematopoietic stem cell transplantation: report from the consensus conference on clinical practice in chronic graft-versus-host disease. Brain. 2010; 133: 2852-2865.
- 129Koeppen S, Thirugnanasambanthan A, Koldehoff M. Neuromuscular complications after hematopoietic stem cell transplantation. Support Care Cancer. 2014; 22: 2337-2341.
- 130Kraus PD, Wolff D, Grauer O, et al. Muscle cramps and neuropathies in patients with allogeneic hematopoietic stem cell transplantation and graft-versus-host disease. PLoS One. 2012; 7: e44922.
- 131Bilic E, Delimar V, Desnica L, et al. High prevalence of small- and large-fiber neuropathy in a prospective cohort of patients with moderate to severe chronic GvHD. Bone Marrow Transplant. 2016; 51: 1513-1517.
- 132Katyal N, Wadhwa A, Bollu PC. Multiple cranial neuropathies in a patient with diffuse large B-cell lymphoma: case report and review of literature. Cureus. 2018; 10: e2186.
- 133Grisold W, Grisold A. Chemotherapy-induced peripheral neuropathy: limitations in current prophylactic/therapeutic strategies and directions for future research. Curr Med Res Opin. 2017; 33: 1291-1292.
- 134Haydaroglu Sahin H, Mete A, Pehlivan M. Neurolymphomatosis in non-Hodgkin lymphoma with cranial multineuritis: a case report. Medicine (Baltimore). 2018; 97: e0303.
- 135Shenoy SB, Karam T, Udupa K, Nayal B. Leukaemic infiltration of the optic nerve head: a rare site of initial relapse. BMJ Case Rep. 2016; 2016. https://doi.org/10.1136/bcr-2016-217239.
- 136Kim JL, Mendoza PR, Rashid A, Hayek B, Grossniklaus HE. Optic nerve lymphoma: report of two cases and review of the literature. Surv Ophthalmol. 2015; 60: 153-165.
- 137Borchard NA, Nayak JV. Orbital apex syndrome. N Engl J Med. 2018; 378: e23.
- 138Alhammad F, Maktabi A, Alkatan HM, Elkhamary SM, Almazyad E, Al-Sheikh O. Isolated superior oblique muscle extranodal marginal zone B cell lymphoma: case report. Saudi J Ophthalmol. 2018; 32: 66-68.
- 139Liu KC, Hennessey MA, McCall CM, Proia AD. Ocular involvement in neurolymphomatosis. Am J Ophthalmol Case Rep. 2018; 10: 148-151.
- 140Tang LJ, Gu CL, Zhang P. Intraocular lymphoma. Int J Ophthalmol. 2017; 10: 1301-1307.
- 141Ogiwara T, Horiuchi T, Sekiguchi N, Kakizawa Y, Hongo K. Primary malignant lymphoma of the trigeminal nerve: case report and literature review. World Neurosurg. 2015; 84(592): e593-e597.
- 142Naridze RL, Selby JC, Link BK, Liu V. Isolated unilateral facial nerve palsy: an unusual manifestation of recurrent diffuse large B-cell lymphoma. J Eur Acad Dermatol Venereol. 2016; 30: 1033-1035.
- 143Torrealba-Acosta G, Gadhia R, Leslie-Mazwi T. A rare neurological complication of Waldenstrom's Macroglobulinemia. J Clin Neurosci. 2018; 48: 143-146.
- 144Kumar K, Ahmed R, Bajantri B, et al. Tumors presenting as multiple cranial nerve palsies. Case Rep Neurol. 2017; 9: 54-61.
- 145Marinelli JP, Modzeski MC, Lane JI, et al. Primary skull base lymphoma: manifestations and clinical outcomes of a great imitator. Otolaryngol Head Neck Surg. 2018;159(4):643-649.
- 146Baskaran RK, Krishnamoorthy, Smith M. Numb chin syndrome--a reflection of systemic malignancy. World J Surg Oncol. 2006; 4: 52.
- 147Cohen J, Laing DG, Wilkes FJ. Taste and smell function in pediatric blood and marrow transplant patients. Support Care Cancer. 2012; 20: 3019-3023.
- 148ElKhamary SM, Galindo-Ferreiro A, AlGhafri L, Khandekar R, Schellini SA. Characterization of diffuse orbital mass using apparent diffusion coefficient in 3-tesla MRI. Eur J Radiol Open. 2018; 5: 52-57.
- 149Meregalli C, Fumagalli G, Alberti P, et al. Neurofilament light chain as disease biomarker in a rodent model of chemotherapy induced peripheral neuropathy. Exp Neurol. 2018; 307: 129-132.
- 150Mariotto S, Farinazzo A, Magliozzi R, Alberti D, Monaco S, Ferrari S. Serum and cerebrospinal neurofilament light chain levels in patients with acquired peripheral neuropathies. J Peripher Nerv Syst. 2018b; 23: 174-177.
- 151Sandelius Å, Zetterberg H, Blennow K, et al. Plasma neurofilament light chain concentration in the inherited peripheral neuropathies. Neurology. 2018; 90: e518-e524.