Pathology of Nerve Biopsy and Diagnostic Yield of PCR-Based Clonality Testing in Neurolymphomatosis

Infiltration of the peripheral nervous system (PNS) by lymphoma, called neurolymphomatosis, is a rare condition among the spectrum of lymphoma-associated neuropathies; its diagnosis is challenging. Cerebrospinal fluid (CSF) analysis is of great value, but nerve biopsy (NB) may be necessary to prove invasion by malignant cells. Clonality polymerase chain reaction (PCR)-based analysis is a validated method in the diagnosis of hematological malignancies, but there are very little data on its diagnostic yield on NB samples. We explored the contribution of NB with clonality analysis to the diagnosis of neurolymphomatosis in 15 patients with negative CSF analysis. Moreover, we assessed the performance of clonality testing in a case-control manner, using patients with inflammatory infiltrates on NB as controls. Neurolymphomatosis was the first manifestation of lymphoma in 60% and could be diagnosed on routine histology alone in 40%. Clonality testing showed monoclonal rearrangement in 86.7% and was unsuccessful in 8.1%. Performance of clonality testing was as follows: 92.9% positive predictive value, 90% negative predictive value, 86.7% sensitivity, 94.7% specificity. This study confirms the diagnostic challenge of neurolymphomatosis, the usefulness of NB in patients with negative CSF analysis, and highlights the high yield of PCR-based clonality testing to assess the malignant nature of PNS lymphoid infiltrates.

[1]  S. Ben-Haim,et al.  FDG PET-CT evaluation in neurolymphomatosis: imaging characteristics and clinical outcomes , 2018, Leukemia & lymphoma.

[2]  S. Swerdlow WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues , 2017 .

[3]  S. Ghorbian Molecular pathology diagnosis of diffuse large B cell lymphoma using BIOMED-2 clonal gene rearrangements. , 2017, Annals of diagnostic pathology.

[4]  J. Bouchal,et al.  Clonality testing of lymphoproliferative disorders in a large cohort of primary and consultant biopsies. , 2017, Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia.

[5]  P. Dyck,et al.  Targeted fascicular biopsy of the brachial plexus: rationale and operative technique. , 2017, Neurosurgical focus.

[6]  Shiyong Li,et al.  Multimodality Technologies in the Assessment of Hematolymphoid Neoplasms. , 2017, Archives of pathology & laboratory medicine.

[7]  A. C. Santos,et al.  18F-FDG PET/CT/MRI Fusion Images Showing Cranial and Peripheral Nerve Involvement in Neurolymphomatosis , 2017, Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India.

[8]  E. Lau,et al.  Neurolymphomatosis: MRI and 18FDG‐PET features , 2016, Journal of medical imaging and radiation oncology.

[9]  E. Wong,et al.  Neurological presentations of intravascular lymphoma (IVL): meta-analysis of 654 patients , 2016, BMC Neurology.

[10]  K. Amrami,et al.  Neurolymphomatosis: A report of 2 cases representing opposite ends of the clinical spectrum , 2015, Muscle & nerve.

[11]  P. Dyck,et al.  Nerve pathologic features differentiate POEMS syndrome from CIDP , 2015, Acta neuropathologica communications.

[12]  L. Richard,et al.  Value of Nerve Biopsy in Patients With Latent Malignant Hemopathy and Peripheral Neuropathy , 2015, Medicine.

[13]  S. Hohaus,et al.  Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature , 2014, Muscle & nerve.

[14]  J. Manning,et al.  Neurolymphomatosis: A case series of clinical manifestations, treatments, and outcomes , 2014, Journal of the Neurological Sciences.

[15]  O. Chinot,et al.  Primary neurolymphomatosis diagnosis and treatment: A retrospective study , 2014, Journal of the Neurological Sciences.

[16]  G. Sobue,et al.  Clinicopathological features of neuropathy associated with lymphoma. , 2013, Brain : a journal of neurology.

[17]  S. Pittock,et al.  Teaching NeuroImages: Diagnostic utility of FDG-PET in neurolymphomatosis , 2013, Neurology.

[18]  S. Treon,et al.  A new era for Waldenstrom macroglobulinemia: MYD88 L265P. , 2013, Blood.

[19]  T. Batchelor,et al.  Diagnosis and Management of Neurolymphomatosis , 2012, Cancer journal.

[20]  E. Schuuring,et al.  EuroClonality/BIOMED-2 guidelines for interpretation and reporting of Ig/TCR clonality testing in suspected lymphoproliferations , 2012, Leukemia.

[21]  T. Maisonobe,et al.  Heterogeneous spectrum of neuropathies in Waldenström's macroglobulinemia: a diagnostic strategy to optimize their management , 2012, Journal of the peripheral nervous system : JPNS.

[22]  J. Baehring,et al.  Neurolymphomatosis , 2004, Journal of Neuro-Oncology.

[23]  C. Lacroix,et al.  Peripheral Nerve Society Guideline on processing and evaluation of nerve biopsies , 2010, Journal of the peripheral nervous system : JPNS.

[24]  M. J. van den Bent,et al.  Neurolymphomatosis: an International Primary CNS Lymphoma Collaborative Group report. , 2010, Blood.

[25]  M. Chamberlain,et al.  Neurolymphomatosis: a rare metastatic complication of diffuse large B-Cell lymphoma , 2009, Journal of Neuro-Oncology.

[26]  N. Raje,et al.  Neurological manifestations of Waldenström macroglobulinemia , 2008, Nature Clinical Practice Neurology.

[27]  David J J de Gorter,et al.  Lymphoma dissemination: the other face of lymphocyte homing. , 2007, Blood.

[28]  T. Maisonobe,et al.  Neuropathy in lymphoma: a relationship between the pattern of neuropathy, type of lymphoma and prognosis? , 2007, Journal of Neurology, Neurosurgery, and Psychiatry.

[29]  W. Erber,et al.  A practical strategy for the routine use of BIOMED‐2 PCR assays for detection of B‐ and T‐cell clonality in diagnostic haematopathology , 2007, British journal of haematology.

[30]  T. Molina,et al.  Polymerase chain reaction-based clonality testing in tissue samples with reactive lymphoproliferations: usefulness and pitfalls. A report of the BIOMED-2 Concerted Action BMH4-CT98-3936 , 2007, Leukemia.

[31]  T. Molina,et al.  Improved reliability of lymphoma diagnostics via PCR-based clonality testing: — Report of the BIOMED-2 Concerted Action BHM4-CT98-3936 , 2007, Leukemia.

[32]  M. Groves,et al.  Primary sciatic nerve lymphoma: a case report and review of the literature , 2006, Journal of Neurology, Neurosurgery & Psychiatry.

[33]  J. Bogousslavsky,et al.  Clinicopathological and molecular biological studies in a patient with neurolymphomatosis , 2000, Muscle & nerve.

[34]  K. Elenitoba-Johnson,et al.  PCR analysis of the immunoglobulin heavy chain gene in polyclonal processes can yield pseudoclonal bands as an artifact of low B cell number. , 2000, The Journal of molecular diagnostics : JMD.

[35]  J. Sabourin,et al.  Inflammatory neuromuscular disorders associated with chronic lymphoid leukemia: Evidence for clonal B cells within muscle and nerve , 1996, Journal of the Neurological Sciences.

[36]  B. Lange,et al.  Detection of minimal disease in hematopoietic malignancies of the B-cell lineage by using third-complementarity-determining region (CDR-III)-specific probes. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[37]  P. Gaulard,et al.  T‐Cell lymphoma revealed by a peripheral neuropathy: A report of two cases with an immunohistologic study on lymph node and nerve biopsies , 1986, Cancer.

[38]  J. Vallat,et al.  Peripheral nerve damage during multiple myeloma and waldenstrom's macroglobulinemia. An ultrastrural and immunopathologic study , 1982, Cancer.

[39]  A. Vital,et al.  A case of mononeuropathy multiplex with type II cryoglobulinemia, necrotizing vasculitis and low grade B cell lymphoma. , 2007, Clinical neuropathology.

[40]  A. Hays,et al.  B cell small lymphocytic lymphoma and chronic lymphocytic leukemia with peripheral neuropathy: two cases with neuropathological findings and lymphocyte marker analysis , 2004, Acta Neuropathologica.