R. Randall, W. Williamson, . Jr, F. Mullinax, and M. Tung, Manifestations of systemic light chain deposition, The American Journal of Medicine, vol.60, issue.2, pp.293-299, 1976.
DOI : 10.1016/0002-9343(76)90440-X

D. Ganeval, L. Noel, . Preud-liomme-'jl, D. Droz, and J. Grunfeld, Light-chain deposition disease: Its relation with AL-type amyloidosis, Kidney International, vol.26, issue.1, pp.1-9, 1984.
DOI : 10.1038/ki.1984.126

J. Lin and G. Markowitz, Valeri AM Renal monoclonal immunoglobulin deposition disease: the disease spectrum, J Am Soc Nephrol, vol.12, pp.1482-1492, 2001.

C. Pozzi, G. Fogazzi, G. Banfi, E. Strom, and C. Ponticelli, Locatelli F Renal disease and patient survival in light chain deposition disease, Clin Nephrol, vol.43, pp.281-287, 1995.

R. Tubbs, G. Gephardt, J. Mcmahon, P. Hall, R. Valenzuela et al., Light chain nephropathy, The American Journal of Medicine, vol.71, issue.2, pp.263-269, 1981.
DOI : 10.1016/0002-9343(81)90127-3

R. Heilman, J. Velosa, K. Holley, K. Offord, and R. Kyle, Long-Term Follow-Up and Response to Chemotherapy in Patients With Light-Chain Deposition Disease, American Journal of Kidney Diseases, vol.20, issue.1, pp.34-41, 1992.
DOI : 10.1016/S0272-6386(12)80314-3

J. Buxbaum, J. Chuba, G. Heilman, A. Solomon, and G. Gallo, Monoclonal Immunoglobulin Deposition Disease: Light Chain and Light and Heavy Chain Deposition Diseases and Their Relation to Light Chain Amyloidosis, Annals of Internal Medicine, vol.112, issue.6, pp.455-464, 1990.
DOI : 10.7326/0003-4819-76-3-112-6-455

A. Khoor, J. Myers, and H. Tazelaar, Amyloid-like Pulmonary Nodules, Including Localized Light-Chain Deposition, American Journal of Clinical Pathology, vol.121, issue.2, pp.200-204, 2004.
DOI : 10.1309/3GECPW2402F6V8EK

S. Morinaga, H. Watanabe, and G. A. , Plasmacytoma of the Lung Associated with Nodular Deposits of Immunoglobulin, The American Journal of Surgical Pathology, vol.11, issue.12, pp.989-995, 1987.
DOI : 10.1097/00000478-198712000-00010

F. Piard and N. Yaziji, Solitary plasmacytoma of the lung with light chain extracellular deposits: a case report and review of the literature, Histopathology, vol.140, issue.4, pp.356-361, 1998.
DOI : 10.1016/0899-7071(94)00033-9

A. Rostagno, G. Frizzera, L. Ylagan, A. Kumar, J. Ghiso et al., Tumoral non-amyloidotic monoclonal immunoglobulin light chain deposits ('aggregoma'): presenting feature of B-cell dyscrasia in three cases with immunohistochemical and biochemical analyses, British Journal of Haematology, vol.155, issue.1, pp.62-69, 2002.
DOI : 10.1023/A:1008375931236

M. Stokes, J. Jagirdar, O. Burchstin, S. Kornacki, A. Kumar et al., Nodular pulmonary immunoglobulin light chain deposits with coexistent amyloid and nonamyloid features in an HIV-infected patient, Mod Pathol, vol.10, pp.1059-1065, 1997.

P. Bhargava and J. Rushin, Pulmonary Light Chain Deposition Disease, The American Journal of Surgical Pathology, vol.31, issue.2, pp.267-276, 2007.
DOI : 10.1097/01.pas.0000213358.18380.d2

M. Colombat, M. Stern, and O. Groussard, Pulmonary Cystic Disorder Related to Light Chain Deposition Disease, American Journal of Respiratory and Critical Care Medicine, vol.173, issue.7, pp.777-780, 2006.
DOI : 10.1164/rccm.200510-1620CR

J. Van-dongen and A. Langerak, Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations: Report of the BIOMED-2 Concerted Action BMH4-CT98-3936, Leukemia, vol.17, issue.12, pp.2257-2317, 2003.
DOI : 10.1038/sj.leu.2403202

P. Evans, C. Pott, and P. Groenen, Significantly improved PCR-based clonality testing in B-cell malignancies by use of multiple immunoglobulin gene targets. Report of the BIOMED-2 Concerted Action BHM4-CT98-3936, Report of the BIOMED-2 Concerted Action BHM4-CT98-3936, pp.207-214, 2007.
DOI : 10.1038/sj.leu.2404479

S. Zompi and L. Couderc, Clonality analysis of alveolar B lymphocytes contributes to the diagnostic strategy in clinical suspicion of pulmonary lymphoma, Blood, vol.103, issue.8, pp.3208-3215, 2004.
DOI : 10.1182/blood-2003-07-2335

V. Giudicelli, D. Chaume, M. Lefranc, and . Imgt-/-v-quest, IMGT/V-QUEST, an integrated software program for immunoglobulin and T cell receptor V-J and V-D-J rearrangement analysis, Nucleic Acids Research, vol.32, issue.Web Server
DOI : 10.1093/nar/gkh412

Y. Monod, M. Giudicelli, V. Chaume, D. Lefranc, M. Imgt-v-j et al., IMGT/JunctionAnalysis: the first tool for the analysis of the immunoglobulin and T cell receptor complex V-J and V-D-J JUNCTIONs, Bioinformatics, vol.20, issue.Suppl 1, pp.379-385, 2004.
DOI : 10.1093/bioinformatics/bth945

M. Lefranc, V. Giudicelli, Q. Kaas, and . Imgt, IMGT, the international ImMunoGeneTics information system(R), Nucleic Acids Research, vol.33, issue.Database issue, pp.593-597, 2005.
DOI : 10.1093/nar/gki065
URL : https://hal.archives-ouvertes.fr/hal-00357158

J. Bienenstock and M. Mcdermott, Bronchus- and nasal-associated lymphoid tissues, Immunological Reviews, vol.166, issue.2, pp.22-31, 2005.
DOI : 10.1046/j.1365-2567.1997.00356.x

R. Bende, W. Aarts, R. Riedl, D. De-jong, and S. Pals, Among B cell non-Hodgkin's lymphomas, MALT lymphomas express a unique antibody repertoire with frequent rheumatoid factor reactivity, The Journal of Experimental Medicine, vol.162, issue.8, pp.1229-1241, 2005.
DOI : 10.1016/0014-4827(89)90405-9

K. Stamatopoulos, C. Belessi, and C. Moreno, Over 20% of patients with chronic lymphocytic leukemia carry stereotyped receptors: pathogenetic implications and clinical correlations, Blood, vol.109, issue.1, pp.259-270, 2007.
DOI : 10.1182/blood-2006-03-012948

B. Messmer, E. Albesiano, and D. Efremov, Multiple Distinct Sets of Stereotyped Antigen Receptors Indicate a Role for Antigen in Promoting Chronic Lymphocytic Leukemia, The Journal of Experimental Medicine, vol.76, issue.4, pp.519-525, 2004.
DOI : 10.1023/A:1008396618983

E. Remstein, A. Dogan, and R. Einerson, The Incidence and Anatomic Site Specificity of Chromosomal Translocations in Primary Extranodal Marginal Zone B-cell Lymphoma of Mucosa-associated Lymphoid Tissue (MALT Lymphoma) in North America, The American Journal of Surgical Pathology, vol.30, issue.12, pp.1546-1553, 2006.
DOI : 10.1097/01.pas.0000213275.60962.2a

N. Leung, D. Lager, M. Gertz, K. Wilson, S. Kanakiriya et al., Long-term outcome of renal transplantation in light-chain deposition disease, American Journal of Kidney Diseases, vol.43, issue.1, pp.147-153, 2004.
DOI : 10.1053/j.ajkd.2003.09.020

E. Kunkel, E. Butcher, and . Plasma, Plasma-cell homing, Nature Reviews Immunology, vol.3, issue.10, pp.822-829, 2003.
DOI : 10.1038/nri1203

C. Thieblemont and F. Berger, Dumontet C Mucosa-associated lymphoid tissue lymphoma is a disseminated disease in one third of 158 patients analyzed, Blood, vol.95, pp.802-806, 2000.

P. Isaacson, M. Piris, F. Berger, B. Nathwani, and S. Swerdlow, Harris NL Editor: Press I Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma). Tumours of haematopoietic and lymphoid tissues, pp.157-160, 2001.

P. Ghia, K. Stamatopoulos, and C. Belessi, Geographic patterns and pathogenetic implications of IGHV gene usage in chronic lymphocytic leukemia: the lesson of the IGHV3-21 gene, Blood, vol.105, issue.4, pp.3-21
DOI : 10.1182/blood-2004-07-2606

F. Ghiotto and F. Fais, Remarkably similar antigen receptors among a subset of patients with chronic lymphocytic leukemia, Journal of Clinical Investigation, vol.113, issue.7, pp.1008-1016, 2004.
DOI : 10.1172/JCI19399DS1

G. Tobin, U. Thunberg, and A. Johnson, Chronic lymphocytic leukemias utilizing the VH3-21 gene display highly restricted V??2-14 gene use and homologous CDR3s: implicating recognition of a common antigen epitope, Blood, vol.101, issue.>12, pp.4952-4957, 2003.
DOI : 10.1182/blood-2002-11-3485

G. Tobin, U. Thunberg, and K. Karlsson, Subsets with restricted immunoglobulin gene rearrangement features indicate a role for antigen selection in the development of chronic lymphocytic leukemia, Blood, vol.104, issue.9, pp.2879-2885, 2004.
DOI : 10.1182/blood-2004-01-0132

G. Widhopf, L. Rassenti, T. Toy, J. Gribben, and W. Wierda, Chronic lymphocytic leukemia B cells of more than 1% of patients express virtually identical immunoglobulins, Blood, vol.104, issue.8, pp.2499-2504, 2004.
DOI : 10.1182/blood-2004-03-0818

A. Traverse-glehen, F. Davi, and B. Simon, Analysis of VH genes in marginal zone lymphoma reveals marked heterogeneity between splenic and nodal tumors and suggests the existence of clonal selection, Haematologica, vol.90, pp.470-478, 2005.

R. Marasca, P. Vaccari, and M. Luppi, Immunoglobulin Gene Mutations and Frequent Use of VH1-69 and VH4-34 Segments in Hepatitis C Virus-Positive and Hepatitis C Virus-Negative Nodal Marginal Zone B-Cell Lymphoma, The American Journal of Pathology, vol.159, issue.1, pp.253-261, 2001.
DOI : 10.1016/S0002-9440(10)61691-4

M. Yoshida and M. Okabe, ImmunoglobulinVH genes in thymic MALT lymphoma are biased toward a restricted repertoire and are frequently unmutated, The Journal of Pathology, vol.89, issue.3, pp.415-422, 2006.
DOI : 10.1002/path.1889

F. Suarez, O. Lortholary, O. Hermine, and M. Lecuit, Infection-associated lymphomas derived from marginal zone B cells: a model of antigen-driven lymphoproliferation, Blood, vol.107, issue.8, pp.3034-3044, 2006.
DOI : 10.1182/blood-2005-09-3679
URL : https://hal.archives-ouvertes.fr/hal-00022498

B. Royer, D. Cazals-hatem, and J. Sibilia, Lymphomas in patients with Sjogren s syndrome are marginal zone B-cell neoplasms, arise in diverse extranodal and nodal sites, and are ' not associated with viruses, Blood, vol.90, pp.766-775, 1997.

G. Derringer, L. Thompson, R. Frommelt, K. Bijwaard, and C. Heffess, Abbondanzo SL Malignant lymphoma of the thyroid gland: a clinicopathologic study of 108 cases

T. Al-saleem, Immunoproliferative small intestinal disease (IPSID): a model for mature B-cell neoplasms, Blood, vol.105, issue.6, pp.2274-2280, 2005.
DOI : 10.1182/blood-2004-07-2755

A. Wotherspoon and C. Doglioni, Regression of primary low-grade B-cell gastric lymphoma of mucosa-associated lymphoid tissue type after eradication of Helicobacter pylori, The Lancet, vol.342, issue.8871, pp.575-577, 1993.
DOI : 10.1016/0140-6736(93)91409-F

A. Wotherspoon, C. Doglioni, M. De-boni, J. Spencer, and P. Isaacson, Antibiotic treatment for low-grade gastric MALT lymphoma, The Lancet, vol.343, issue.8911, p.1503, 1994.
DOI : 10.1016/S0140-6736(94)92613-1

B. Kutting, G. Bonsmann, D. Metze, and T. Luger, Borrelia burgdorferi???associated primary cutaneous B cell lymphoma: complete clearing of skin lesions after antibiotic pulse therapy or intralesional injection of interferon alfa-2a, Journal of the American Academy of Dermatology, vol.36, issue.2, pp.311-314, 1997.
DOI : 10.1016/S0190-9622(97)80405-7

E. Roggero, E. Zucca, and C. Mainetti, Eradication of Borrelia burgdorferi infection in primary marginal zone B-cell lymphoma of the skin, Human Pathology, vol.31, issue.2, pp.263-268, 2000.
DOI : 10.1016/S0046-8177(00)80233-6

O. Hermine, F. Lefrere, and J. Bronowicki, Regression of Splenic Lymphoma with Villous Lymphocytes after Treatment of Hepatitis C Virus Infection, New England Journal of Medicine, vol.347, issue.2, pp.89-94, 2002.
DOI : 10.1056/NEJMoa013376

C. Hallas, A. Greiner, and K. Peters, Muller-Hermelink HK Immunoglobulin VH genes of high-grade mucosa-associated lymphoid tissue lymphomas show a high load of somatic mutations and evidence of antigen-dependent affinity maturation, Lab Invest, vol.78, pp.277-287, 1998.

T. Papadaki, K. Stamatopoulos, and C. Belessi, Splenic Marginal-zone Lymphoma: One or More Entities? A Histologic, Immunohistochemical, and Molecular Study of 42 Cases, The American Journal of Surgical Pathology, vol.31, issue.3, pp.438-446, 2007.
DOI : 10.1097/01.pas.0000213419.08009.b0

W. Funkhouser and R. Warnke, Preferential IgH V4-34 gene segment usage in particular subtypes of B-cell lymphoma detected by antibody 9G4, Human Pathology, vol.29, issue.11, pp.1317-1321, 1998.
DOI : 10.1016/S0046-8177(98)90264-7

C. Chapman, D. Wright, H. Feizi, Z. Davis, and F. Stevenson, VH gene analysis of Burkitt's lymphoma in children from north-western Iran, British Journal of Haematology, vol.79, issue.4, pp.1116-1123, 1998.
DOI : 10.1002/(SICI)1096-9896(199706)182:2<125::AID-PATH843>3.0.CO;2-9

T. Sekita, J. Tamaru, K. Kaito, T. Katayama, and M. Kobayashi, Primary Central Nervous System Lymphomas Express Vh Genes with Intermediate to High Somatic Mutations, Leukemia & Lymphoma, vol.77, issue.3-4, pp.377-385, 2001.
DOI : 10.1038/382462a0

I. Losses and A. Alizadeh, Eisen MB Ongoing immunoglobulin somatic mutation in germinal center B cell-like but not in activated B cell-like diffuse large cell lymphomas

I. Losses and C. Okada, Tibshirani R Molecular analysis of immunoglobulin genes in diffuse large B-cell lymphomas, Blood, vol.95, pp.1797-1803, 2000.

L. Silberstein, A. George, and J. Durdik, The V4-34 Encoded Anti-i Autoantibodies Recognize a Large Subset of Human and Mouse B-Cells, Blood Cells, Molecules, and Diseases, vol.22, issue.2, pp.126-138, 1996.
DOI : 10.1006/bcmd.1996.0020

F. Stevenson, C. Longhurst, and C. Chapman, Utilization of the VH4-21 Gene Segment by Anti-DNA Antibodies from Patients with Systemic Lupus Erythematosus, Journal of Autoimmunity, vol.6, issue.6, pp.809-825, 1993.
DOI : 10.1006/jaut.1993.1066

V. Pascual, I. Randen, and K. Thompson, The complete nucleotide sequences of the heavy chain variable regions of six monospecific rheumatoid factors derived from Epstein-Barr virus-transformed B cells isolated from the synovial tissue of patients with rheumatoid arthritis. Further evidence that some autoantibodies are unmutated copies of germ line genes., Journal of Clinical Investigation, vol.86, issue.4, pp.1320-1328, 1990.
DOI : 10.1172/JCI114841

A. Pugh-bernard and G. Silverman, Regulation of inherently autoreactive VH4-34 B cells in the maintenance of human B cell tolerance, Journal of Clinical Investigation, vol.108, issue.7, pp.1061-1070, 2001.
DOI : 10.1172/JCI200112462

P. Kraj, D. Friedman, and F. Stevenson, Silberstein LE Evidence for the overexpression of the VH4-34 (VH4.21) Ig gene segment in the normal adult human peripheral blood B cell repertoire, J Immunol, vol.154, pp.6406-6420, 1995.

J. Miklos and S. Swerdlow, Bahler DW Salivary gland mucosa-associated lymphoid tissue lymphoma immunoglobulin V(H) genes show frequent use of Vl-69 with distinctive CDR3 features, Blood, vol.95, pp.3878-3884, 2000.

P. Oppezzo, C. Magnac, and S. Bianchi, Do CLL B cells correspond to naive or memory B-lymphocytes? Evidence for an active Ig switch unrelated to phenotype expression and Ig mutational pattern in B-CLL cells, Leukemia, vol.16, issue.12, pp.2438-2446, 2002.
DOI : 10.1038/sj.leu.2402731

K. Toellner, W. Jenkinson, and D. Taylor, Low-level Hypermutation in T Cell???independent Germinal Centers Compared with High Mutation Rates Associated with T Cell???dependent Germinal Centers, The Journal of Experimental Medicine, vol.35, issue.3, pp.383-389, 2002.
DOI : 10.1073/pnas.98.3.1166

T. Grogan, R. Kyle, H. Muller-hemerlink, N. Harris, and . Editor, Press I Plasma cell neoplasm. Tumours of haematopoietic and lymphoid tissues, pp.142-156, 2001.

L. Denoroy and S. Deret, Overrepresentation of the V??IV subgroup in light chain deposition disease, Immunology Letters, vol.42, issue.1-2, pp.63-66, 1994.
DOI : 10.1016/0165-2478(94)90036-1