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1. A descriptive study of IgG4-related disease in children and young adults

Author

de Sainte Marie, B., Ebbo, M., Grados, A., Rebours, V., Reumaux, H., Briantais, A., Urbina, D., Cury, J., Morel, N., Lhote, F., Rohmer, B., Lazaro, E., Agbo-Kpati, K.P., Deroux, A., Domont, F., Delacroix, I., Lavigne, C., Perlat, A., Kahn, J.E., Godeau, B., Hamidou, M., Launay, D., Bader-Meunier, B., and Schleinitz, N.

Published
2022
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4. Pulmonary vasculitides

Author

Mouthon, L., Lhote, F., Guillevin, L., Ansell, B. M., editor, Bacon, P. A., editor, Lie, J. T., editor, and Yazici, H., editor

Published
1996
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7. La maladie associée aux IgG4 à début pédiatrique ou « juvénile » existe-t-elle ? A propos d’une série descriptive de 25 cas

Author

De Sainte Marie, B., primary, Bader-Meunier, B., additional, Rebours, V., additional, Hamidou, M., additional, Lazaro, E., additional, Rohmer, B., additional, Morel, N., additional, Deroux, A., additional, Agbo-Kpati, K.P., additional, Urbina, D., additional, Lhote, F., additional, Ebbo, M., additional, and Schleinitz, N., additional

Published
2020
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20. Impact des dilatations des bronches sur les caractéristiques cliniques et le pronostic des vascularites à ANCA : résultats d’une série de 61 patients

Author

Chilles, M., primary, Lhote, R., additional, Brillet, P.Y., additional, Groh, M., additional, Puechal, X., additional, Cohen-Aubart, F., additional, Delbre, X., additional, Guilpain, P., additional, Barda, T., additional, De Boysson, H., additional, Duhaut, P., additional, Dominique, S., additional, Hachulla, E., additional, Hamidou, M., additional, Subra, J.F., additional, Lifermann, F., additional, Fain, O., additional, Cohen, P., additional, Lhote, F., additional, Nunes, H., additional, Mathian, A., additional, Catherinot, E., additional, Terrier, B., additional, Le Quellec, A., additional, Legendre, C., additional, Cottin, V., additional, Amoura, Z., additional, Couderc, L.J., additional, Diot, E., additional, Guillevin, L., additional, and Tcherakian, C., additional

Published
2018
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21. Détermination de sous-classes phénotypiques de la maladie de Behçet par la méthode d’analyse « cluster » : une étude multicentrique de 496 cas

Author

Fraison, J.B., primary, Mahr, A., additional, Rivière, S., additional, Mura, F., additional, Jorgensen, C., additional, Lhote, F., additional, Dhôte, R., additional, Bourgarit-Durand, A., additional, Fain, O., additional, Mouthon, L., additional, Brézin, A., additional, and Terrier, B., additional

Published
2017
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26. Treatment of antineutrophil cytoplasm autoantibody-associated systemic vasculitis: initiatives of the European Community Systemic Vasculitis Clinical Trials Study Group

Author

Jayne, D, Rasmussen, N, Abramowicz, D, Tesar, V, Petersen, J, Juhl, B, Wiik, A, Gronhagenriska, C, Guillevin, L, Lhote, F, Landais, P, Lesavre, P, Vanhille, P, Andrassy, K, Degroot, K, Gross, W, Vanderwoude, F, Boki, K, Tervaert, J, Kallenberg, C, Vanes, L, Hermans, J, Siegert, C, Hagen, E, Feighery, C, Gregorini, G, Ferrario, F, Dadoniene, J, Vasconcelos, C, Mirapeix, E, Heigl, Z, Pettersson, E, Westman, K, Bacon, P, Savage, C, Lockwood, C, Luqmani, R, Gaskin, G, Pusey, C, Specks, U., SINICO, RENATO ALBERTO, Jayne, D, Rasmussen, N, Abramowicz, D, Tesar, V, Petersen, J, Juhl, B, Wiik, A, Gronhagenriska, C, Guillevin, L, Lhote, F, Landais, P, Lesavre, P, Vanhille, P, Andrassy, K, Degroot, K, Gross, W, Vanderwoude, F, Boki, K, Tervaert, J, Kallenberg, C, Vanes, L, Hermans, J, Siegert, C, Hagen, E, Feighery, C, Gregorini, G, Ferrario, F, Sinico, R, Dadoniene, J, Vasconcelos, C, Mirapeix, E, Heigl, Z, Pettersson, E, Westman, K, Bacon, P, Savage, C, Lockwood, C, Luqmani, R, Gaskin, G, Pusey, C, and Specks, U

Subjects
Vasculitis, medicine.medical_specialty, International Cooperation, PLASMA-EXCHANGE, Birmingham Vasculitis Activity Score, PULSE CYCLOPHOSPHAMIDE, DISEASE-ACTIVITY, Methylprednisolone, Severity of Illness Index, Drug Administration Schedule, Antibodies, Antineutrophil Cytoplasmic, law.invention, Randomized controlled trial, Adrenal Cortex Hormones, law, Azathioprine, Necrotizing Vasculitis, medicine, Humans, Intensive care medicine, Cyclophosphamide, Anti-neutrophil cytoplasmic antibody, Clinical Trials as Topic, business.industry, NECROTIZING VASCULITIS, General Medicine, medicine.disease, Europe, Clinical trial, POLYARTERITIS, Methotrexate, Immunology, IMMUNOGLOBULIN, INTRAVENOUS GAMMA-GLOBULIN, MICROSCOPIC, WEGENERS GRANULOMATOSIS, Microscopic polyangiitis, business, RAPIDLY PROGRESSIVE GLOMERULONEPHRITIS, Immunosuppressive Agents, CYCLOPHOSPHAMIDE THERAPY, Systemic vasculitis
Abstract

The diagnosis, treatment, and monitoring of the primary systemic vasculitides associated with circulating antineutrophil cytoplasm autoantibodies (ANCA) have formed the focus of a multicenter collaborative study. Consensus has been reached on criteria for classification, clinical subgroupings by extent and severity of disease, and ''standard'' and ''best alternative'' therapeutic regimens. Two series of randomized controlled trials have been designed; their aims are (1) to harmonize current approaches to treatment and (2) to test the value of newer therapeutic agents, In support of these trials, semiobjective scoring systems have been created and validated, and previous standardization of ANCA serologic and histologic analysis has been adopted. The systems of classification and clinical management described herein represent the recommendations of a multidisciplinary study group that hopes to improve the outcome of patients with primary systemic vasculitis by wide dissemination of the collective experience from interested centers.

Published
1997

35. Clinical nephrology-epidemiology-clinical trials: Determinants of outcome in ANCA-associated glomerulonephritis: A prospective clinico-histopathological analysis of 96 patients

Author

Hauer, Herbert A., Bajema, Ingeborg M., Van Houwelingen, Hans C., Ferrario, Franco, Noã«l, Laure Hélène, Waldherr, Rã¼diger, Jayne, David R. W., Rasmussen, Niels, Bruijn, Jan A., Hagen, E. Christiaan, Rasmussen, N., Jayne, D. R. W., Neumann, I., Mad Houn, P., Sennesael, J., Tesar, V., Rychlik, I., Bartunkova, J., Luk, J., Juhl, B. Ravn, Petersen, J., Andersen, C. B., Szpirt, W., Wiik, A., Lokkegaard, H., Nielsen, H., Ring, T., Sorensen, S. Freiesleben, Bacon, P. A., Exley, A., Savage, C. O. S., Gaskin, G., Pusey, C., Lockwood, C. M., Luq Mani, R., Gronhagen Riska, C., Ekstrand, A., Guillevin, L., Lhote, F., Lesavre, P., Noel, L. H., Landais, P., Vanhille, P., Bataille, P., Esnault, V., Woude, F. Van Der, Waldherr, R., Schmitt, W., Andrassy, K., Hergesell, O., Nowack, R., Groot, K. De, Herlyn, K., Gross, W. L., Boki, K. A., Boletis, J. N., Emmanouel, D. S., Feighery, C., Ferra Rio, Y., Sinico, R. A., Gregorini, G., Dadoniene, J., Hagen, E. C., Kallenberg, C. G. M., Stegeman, C., Tervaert, J. W. Cohen, Verburgh, C. A., Siegert, C. E. H., Bruijn, J. A., Hauer, H. A., Hermans, J., Houwelingen, J. C. Van, Vergunst, C. E., Gurp, E. Van, Bajema, I. M., Vasconcelos, C., Mirapeix, E., Sole, M., Petterson, E. E., Bruchfeld, A., Westman, K. W. A., Heigl, Z., Chizzolini, C., Maclahan, D., Depierreux, M., van Damme, B., Stejskalova, A., Vernerova, Z., Tornroth, T., Feller, A. C., Gaffney, E., Tardanico, R., Consalonieri, R., Garibotto, Giacomo, Tiebosch, A. T. M. G., Kooijman, C. D., Arques, M. S., Algaba, F., Carreras, M., Perez, M. Vaquero, Bernardo, L., Sundelin, B., Alm, P., Wernersson, A., Veress, B., Landells, W., Howie, A. J., Fleming, S., Griffith, A. P., Furness, P. N., Cook, H. T., Hauer, H, Bajema, I, Van Houwelingen, H, Ferrario, F, Noël, L, Waldherr, R, Jayne, D, Rasmussen, N, Bruijn, J, Hagen, E, Neumann, I, Mad Houn, P, Sennesael, J, Tesar, V, Rychlik, I, Bartunkova, J, Luk, J, Juhl, B, Petersen, J, Andersen, C, Szpirt, W, Wiik, A, Lokkegaard, H, Nielsen, H, Ring, T, Sorensen, S, Bacon, P, Exley, A, Savage, C, Gaskin, G, Pusey, C, Lockwood, C, Luq Mani, R, Gronhagen Riska, C, Ekstrand, A, Guillevin, L, Lhote, F, Lesavre, P, Noel, L, Landais, P, Vanhille, P, Bataille, P, Esnault, V, Woude, F, Schmitt, W, Andrassy, K, Hergesell, O, Nowack, R, Groot, K, Herlyn, K, Gross, W, Boki, K, Boletis, J, Emmanouel, D, Feighery, C, Ferra Rio, Y, Sinico, R, Gregorini, G, Dadoniene, J, Kallenberg, C, Stegeman, C, Tervaert, J, Verburgh, C, Siegert, C, Hermans, J, Houwelingen, J, Vergunst, C, Gurp, E, Vasconcelos, C, Mirapeix, E, Sole, M, Petterson, E, Bruchfeld, A, Westman, K, Heigl, Z, Chizzolini, C, Maclahan, D, Depierreux, M, van Damme, B, Stejskalova, A, Vernerova, Z, Tornroth, T, Feller, A, Gaffney, E, Tardanico, R, Consalonieri, R, Garibotto, G, Tiebosch, A, Kooijman, C, Arques, M, Algaba, F, Carreras, M, Perez, M, Bernardo, L, Sundelin, B, Alm, P, Wernersson, A, Veress, B, Landells, W, Howie, A, Fleming, S, Griffith, A, Furness, P, and Cook, H

Subjects
Prognosi, Biopsy, Antineutrophil Cytoplasmic, Predictive Value of Test, Antibodies, Antibodies, Antineutrophil Cytoplasmic, Immunosuppressive Agent, Glomerulonephritis, Predictive Value of Tests, Recurrence, Azathioprine, Humans, Prospective Studies, Microscopic polyangiiti, Glomerulonephriti, Microscopic polyangiitis, Cyclophosphamide, Pauci-immune crescentic necrotizing glomerulonephritis, Medicine (all), Granulomatosis with Polyangiitis, Prognosis, Wegener's granulomatosis, ANCA-associated vasculiti, Prospective Studie, Treatment Outcome, ANCA-associated vasculitis, Renal biopsy, Glomerular Filtration Rate, Immunosuppressive Agents, Sample Size, Nephrology, Wegener's granulomatosi, Pauci-immune crescentic necrotizing glomerulonephriti, Granulomatosis with Polyangiiti, Human
Abstract

Background. The predictive value of clinical and renal histological features for renal outcome in patients with anti-neutrophil cytoplasmic autoantibody (ANCA)-associated glomerulonephritis was investigated in a prospective analysis of 96 patients with ANCA-associated vasculitis, and moderate renal involvement (creatinine

Published
2002

40. Subacute bacterial endocarditis presenting as polymyalgia rheumatica or giant cell arteritis

Author

Auzary C, Le Thi Huong D, Delarbre X, Sbai A, Lhote F, Papo T, Wechsler B, Patrice Cacoub, Martin-Hunyadi C, and Jc, Piette

Subjects
Male, Giant Cell Arteritis, Heart Valve Diseases, Pain, Middle Aged, Anti-Bacterial Agents, Diagnosis, Differential, Endocarditis, Subacute Bacterial, Adrenal Cortex Hormones, Polymyalgia Rheumatica, Streptococcal Infections, Humans, Diagnostic Errors, Musculoskeletal System, Aged
Abstract

To report on several patients with subacute bacterial endocarditis who were initially presumed, incorrectly, to have polymyalgia rheumatica or giant cell arteritis.We report 3 cases of subacute streptococcal endocarditis mimicking giant cell arteritis in 2 cases and polymyalgia rheumatica in one. We reviewed the literature through Medline search of French and English-language articles published between 1966 and 2005 and found 5 similar cases.Shoulder and/or pelvic girdle pain was associated with neck or back pain in all patients. Scalp tenderness, bilateral jaw pain, amaurosis fugax were present in 2 patients. One patient had no fever. Two patients were treated with corticosteroids with initial good clinical response in one. Appropriate antibiotic therapy resulted in the rapid disappearance of rheumatic complaints in 2 patients and achieved a definitive cure of endocarditis in all cases.Rheumatologic symptoms may hinder the correct diagnosis of infective endocarditis in patients who present with a clinical picture suggesting polymyalgia rheumatica or giant cell arteritis. In such cases, blood cultures should be systematically drawn.

Published
2006

44. Na sulfonate resins and continuous centrifugation: a combined recommended method for clay fractionation (soils, muds and suspensions)

Author

Burtin, G., Portal, J.M., Lhote, F., Leviandier, T., Schiavon, Michel, Bartoli, François, Centre National de la Recherche Scientifique (CNRS), Hydrologie (UR HYAN), Centre national du machinisme agricole, du génie rural, des eaux et forêts (CEMAGREF), ENSAIA NANCY, Partenaires IRSTEA, Institut national de recherche en sciences et technologies pour l'environnement et l'agriculture (IRSTEA)-Institut national de recherche en sciences et technologies pour l'environnement et l'agriculture (IRSTEA), and Irstea Publications, Migration

Subjects
[SDE] Environmental Sciences, CEMAGREF, HYAN, [SDE]Environmental Sciences
Abstract

A combined clay dispersion and fractionation methodology using Na resins and continuous centrifugation was applied to soils and suspended matter transported by runoff or by brooks. The finest, Une méthodologie combinée de dispersion et d'ultrafractionnement d'argiles, utilisant les résines sulfonates Na et la centrifugation en continu, a été appliquée aux sols et aux suspensions d'eaux de ruissellement ou de ruisseaux. Dans les agrosystèmes tempérés, les fractions argileuses les plus fines

Published
1997

45. Persistence of antineutrophil cytoplasmic antibodies (ANCA) in asymptomatic patients with systemic polyarteritis nodosa or Churg-Strauss syndrome: follow-up of 53 patients

Author

Cohen P, Guillevin L, Laurence Baril, Lhote F, Lh, Noel, and Lesavre P

Subjects
Aged, 80 and over, Male, Time Factors, Churg-Strauss Syndrome, Middle Aged, Prognosis, Antibodies, Antineutrophil Cytoplasmic, Polyarteritis Nodosa, Recurrence, Humans, Female, Biomarkers, Aged, Autoantibodies
Abstract

We retrospectively analyzed the significance of persistent ANCA positivity after clinical remission in 53 consecutive patients with histologically and/or angiographically proven polyarteritis nodosa (PAN), or Churg-Strauss syndrome (CSS) followed between 1981 and 1993.ANCA were detected using an immunofluorescence assay and ELISA: Each patient met the American College of Rheumatology 1990 criteria for PAN or CSS. Clinical and biological evaluations were always essential factors in the decision to intensify therapy.ANCA were initially present in 15 patients (28.3%): 3/26 (11.5%) with HBV-related PAN, 6/18 (33.3%) with PAN of unknown etiology and 6/9 (66.7%) with CSS. Five patients remained ANCA-positive after clinical remission: 3 with PAN (one of them relapsed) and 2 with CSS who both relapsed. Among the 12 patients who died during follow-up, only 1 (8.3%) was initially ANCA-positive. Fifteen of the 41 survivors (29.2%) were ANCA-positive.Persistence of ANCA positivity in PAN and CSS may be a marker of an underlying disease process, but does not adequately reflect disease activity and, thus, in no case should be the only indication for therapeutic intensification.

Published
1995

46. Les pachyméningites crâniennes : 28 observations

Author

Boukari, L., primary, Stirnemann, J., additional, Haroche, J., additional, Lhote, F., additional, Larroche, C., additional, Lachenal, F., additional, Boutin-Le Thi Huong, D., additional, Bergmann, J.-F., additional, Cordier, J.-F., additional, Guillevin, L., additional, Rousset, H., additional, and Fain, O., additional

Published
2011
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47. Polyarteritis nodosa and mixed cryoglobulinaemia related to hepatitis B and C virus coinfection. (Concise Reports)

Author

de La Pena Lefebvre, P Garcia, Mouthon, L, Cohen, P, Lhote, F, and Guillevin, L

Subjects
Vasculitis -- Causes of -- Complications and side effects -- Analysis, Cryoglobulinemia -- Complications and side effects -- Analysis, Periarteritis nodosa -- Complications and side effects -- Analysis, Comorbidity -- Analysis -- Complications and side effects, Hepatitis B -- Complications and side effects -- Analysis, Hepatitis C -- Complications and side effects -- Analysis, Health
Abstract

Abstract Objective--To determine the responsibility of hepatitis B virus (HBV) and hepatitis C virus (HCV) and therapeutic implications in a patient who developed systemic vasculitis. Case report--The case of a [...]

Published
2001

50. [Acute renal insufficiency associated with lymphoma. A new case]

Author

Cohen P, Lhote F, Casassus P, Jarrousse B, Marie-Christophe Boissier, Meyrier A, Callard P, and Guillevin L

Subjects
Male, Recurrence, Lymphoma, Non-Hodgkin, Humans, Acute Kidney Injury, Middle Aged, Kidney, Tomography, X-Ray Computed
Abstract

We report on a case of acute renal failure secondary to relapse of a centrocytocentroblastic non-Hodgkin's lymphoma. Twenty-seven cases of acute renal failure due to lymphomatous infiltration of the kidneys have been so far reported. The clinical presentation is non-specific; the size of the kidneys appears normal or enlarged; diagnosis is confirmed by renal biopsy and/or CT scan examination. Chemotherapy and/or radiotherapy sometimes lead to dramatic improvement of renal function. However, prognosis is poor, mostly due to lymphomatous evolution.

Published
1992

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