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Your search keyword '"Bélénotti, P."' showing total 45 results
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45 results on '"Bélénotti, P."'

1. Essai randomisé, contrôle et en double aveugle sur l’impact de la rosuvastatine sur les marqueurs d’athérosclérose infra-clinique chez les patients atteints de vascularite associée aux ANCA

Author

Terrier, B., Pugnet, G., Sirieix, M.E., Quéméneur, T., Puéchal, X., Maurier, F., Néel, A., Benhamou, Y., Bonnotte, B., Schmidt, J., Michon, A., Baudet, A., Charles, P., Cohen-Aubart, F., De Moreuil, C., Dernis, E., Belenotti, P., Ruivard, M., Aumaître, O., Fain, O., Seror, R., Durel, C.A., Jourde-Chiche, N., Lazaro, E., Armengol, G., Bellien, J., Ravaud, P., Baron, G., and Guillevin, L.

Published
2023
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3. Un fossoyeur qui reste de marbre

Author

Bélénotti, P., primary, Moureau, J.-P., additional, Vacheret, H., additional, Piro, J., additional, Vivarrat-Perrin, L., additional, Benyamine, A., additional, and Guilpain, P., additional

Published
2018
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4. Forme pseudo-pathomimique de granulomatose avec polyangéite (anciennement maladie de Wegener)

Author

Ene, N., Bélénotti, P., Benyamine, A., Sovaila, S., Ben Sahla Talet, M.H., Kaminsky, P., Serratrice, J., Weiller, P.-J., Service de Médecine Interne (MARSEILLE - Med Int), Assistance Publique - Hôpitaux de Marseille (APHM), Service de Médecine Interne et Vasculaire [CHRU Nancy], Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy), Développement, Adaptation et Handicap. Régulations cardio-respiratoires et de la motricité (DevAH), and Université de Lorraine (UL)

Subjects
Anticorps anti-cytoplasme des polynucléaires, Wegener granulomatosis, Breast tumor, Maladie de Wegener, Granulomatosis with polyangiitis, Granulomatose avec polyangéite, Tumeur mammaire, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology, Anti-neutrophil cytoplasmic antibody
Abstract

International audience; IntroductionANCA vasculitis may involve the skin and develop slowly without specific histology, and without autoantibodies.Case reportWe report a 50-year-old woman who experienced bilateral mastectomy because of ulcero-necrotic, non-specific inflammatory cutaneous lesions of the breasts. First considered by others as a malinger patient, she developed oto-neurological lesions leading to the diagnosis of Wegener's granulomatosis. Five years later, specific antibodies of the disease were present.ConclusionCutaneous involvement by ANCA vasculitis can be isolated for a long time. Physicians must have a high degree of suspicion to avoid diagnostic delay of ANCA vasculitis.; IntroductionUne granulomatose avec polyangéite peut débuter par une atteinte cutanée isolée et torpide. L’analyse histologique peut alors être totalement aspécifique et les anticorps anti-cytoplasme des polynucléaires absents.ObservationNous rapportons l’observation d’une patiente de 50 ans qui avait subit une mastectomie bilatérale, devant des lésions ulcéro-nécrotiques sans diagnostic. Longtemps considérée par d’autres comme pathomimique, elle développait par la suite une atteinte otoneurologique spécifique de granulomatose avec polyangéite. Les auto-anticorps, quant à eux, ne se positivaient que cinq ans plus tard.ConclusionUne granulomatose avec polyangéite peut parfois avoir une évolution très torpide et le diagnostic peut en être largement retardé. Il ne faut pas conclure trop vite à une pathomimie devant une lésion cutanée qui ne cicatrise pas.

Published
2014

9. Traiter une toux, c’est simple…

Author

Bélénotti, P., primary, Benyamine, A., additional, Séguier, J., additional, Astoul, P., additional, Grandval, P., additional, Gaubert, J.-Y., additional, Serratrice, J., additional, Weiller, P.-J., additional, Terrier, B., additional, and Lachaud, A., additional

Published
2013
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11. Il faut dénuder les fièvres nues

Author

Lachaud, A., primary, Bouvier, C., additional, Seguier, J., additional, Rochwerger, R., additional, Bélénotti, P., additional, Swiader, L., additional, Ene, N.-D., additional, Duffaut, F., additional, Serratrice, J., additional, and Weiller, P.-J., additional

Published
2013
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18. Hétérozygotie C282Y/H63D : réalité de la surcharge en fer évaluée par l’IRM, caractéristiques cliniques et prise en charge de 40 patients

Author

Bélénotti, P., primary, Bernit, E., additional, Benyamine, A., additional, Khibri, H., additional, Gerolami, V., additional, Swiader, L., additional, Ene, N.-D., additional, Poullin, P., additional, Petit, P., additional, Serratrice, J., additional, Harle, J.-R., additional, and Weiller, P.-J., additional

Published
2012
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24. TEP Leopard, Rosai Dorfman dans sa forme floride

Author

Melenotte, C., primary, Bélénotti, P., additional, Tessonier, L., additional, Michel, J., additional, Chetaille, B., additional, Jolibert, M., additional, Dubois, M., additional, Dessi, P., additional, Serratrice, J., additional, and Weiller, P.J., additional

Published
2012
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25. Une douleur chronique vite réglée

Author

Bélénotti, P., primary, Sarlon-Bartoli, G., additional, Migerel, M., additional, Arthuis, M., additional, Benyamine, A., additional, Ene, N., additional, Serratrice, J., additional, Weiller, P.-J., additional, and Delluc, A., additional

Published
2012
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29. Dysphonie et connectivite : savoir prêter l’oreille

Author

Bélénotti, P., primary, Lagier, A., additional, Benyamine, A., additional, Arthuis, M., additional, Moreddu, E., additional, Migerel, M., additional, Ene, N., additional, Serratrice, J., additional, Giovanni, A., additional, and Weiller, P.J., additional

Published
2011
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30. Tout est dans la chronologie…

Author

Bélénotti, P., primary, Benyamine, A., additional, Bensahla, H., additional, Ene, N., additional, Sevy, A., additional, Attarian, S., additional, Serratrice, J., additional, Pouget, J., additional, Weiller, P.-J., additional, and Krolak-Salmon, P., additional

Published
2010
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34. Caractéristiques cliniques et thérapeutiques des vascularites urticariennes hypocomplémentémiques : étude nationale multicentrique rétrospective

Author

Jachiet, M., Flageul, B., Deroux, A., Le Quellec, A., Maurier, F., Cordoliani, F., Godmer, P., Abasq, C., Astudillo, L., Belenotti, P., Bessis, D., Bigot, A., Doutre, M.-S., Ebbo, M., Guichard, I., Hachulla, E., Héron, E., Jeudy, G., Jourde-Chiche, N., Jullien, D., Lavigne, C., Machet, L., Macher, M.-A., Martel, C., Melboucy-Belkhir, S., Morice, C., Petit, A., Simorre, B., Zenone, T., Bouillet, L., Bagot, M., Frémeaux-Bacchi, V., Guillevin, L., Mouthon, L., Dupin, N., Aractingi, S., and Terrier, B.

Published
2014
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37. Vena Cava Filter Migration: An Unappreciated Complication. About Four Cases and Review of the Literature

Author

Bélénotti, Pauline, Sarlon-Bartoli, Gabrielle, Bartoli, Michel-Alain, Benyamine, Audrey, Thevenin, Benjamin, Muller, Cyril, Serratrice, Jacques, Magnan, Pierre-Edouard, and Weiller, Pierre-Jean

Abstract

Inferior vena cava filter placement is performed to prevent pulmonary risk secondary to deep venous thrombosis. Indications for this treatment are limited to patients experiencing recurrences under well-managed anticoagulant treatment or presenting with contraindication to anticoagulant treatment. Nowadays, as these clinical situations are rare, this device is less and less used, all the more since, for several years now, thrombosis, fracture, or infectious complications as well as filter migration have been reported. Filter migrations are responsible for atypical and varied clinical presentations likely to defer diagnosis. To treat them, the filter is extracted, which is very risky in patients with a thromboembolic history. In our center, during a period of 14 years, we retrospectively collected and studied partial or complete vena cava filter migration cases that had been treated by extraction. We are reporting four very different clinical cases and, more specifically, the second published case of migration to a renal vein, which mimicked a systemic disease. Because of its very atypical clinical presentations, cava filter migration is an unappreciated and certainly underdiagnosed complication. However, this complication must not question cava filter placement when it is justified. In contrast, it prompts early filter extraction or long-term radiological surveillance.

Published
2011
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38. [Diffuse pain in a 63-year-old man].

Author

Bélénotti P, Moureau JP, Vacheret H, Piro J, Vivarrat-Perrin L, Benyamine A, and Guilpain P

Subjects
Chronic Pain etiology, Diagnosis, Differential, Humans, Male, Middle Aged, Scleredema Adultorum complications, Chronic Pain diagnosis, Scleredema Adultorum diagnosis
Published
2018
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39. [Asthenia, weight loss and abdominal pain in a 64-year-old woman].

Author

Bernard C, Bailly F, Craigherot F, Bancel B, Brevet M, Broussolle C, Sève P, and Bélénotti P

Subjects
Abdominal Pain complications, Acute-Phase Reaction diagnosis, Asthenia complications, Castleman Disease complications, Diagnosis, Differential, Female, Humans, Liver Diseases complications, Middle Aged, Abdominal Pain diagnosis, Asthenia diagnosis, Castleman Disease diagnosis, Liver Diseases diagnosis, Weight Loss physiology
Published
2015
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41. [Granulomatosis with polyangiitis (previously Wegener's granulomatosis) mimicking malingering].

Author

Ene N, Bélénotti P, Benyamine A, Sovaila S, Ben Sahla Talet MH, Kaminsky P, Serratrice J, and Weiller PJ

Subjects
Biomarkers blood, Breast pathology, Delayed Diagnosis, Diagnosis, Differential, Drug Therapy, Combination, Female, Glucocorticoids therapeutic use, Granulomatosis with Polyangiitis blood, Granulomatosis with Polyangiitis drug therapy, Granulomatosis with Polyangiitis surgery, Humans, Immunosuppressive Agents adverse effects, Immunosuppressive Agents therapeutic use, Malingering, Mastectomy, Middle Aged, Treatment Failure, Treatment Outcome, Antibodies, Antineutrophil Cytoplasmic blood, Granulomatosis with Polyangiitis diagnosis, Immunologic Factors blood
Abstract

Introduction: ANCA vasculitis may involve the skin and develop slowly without specific histology, and without autoantibodies., Case Report: We report a 50-year-old woman who experienced bilateral mastectomy because of ulcero-necrotic, non-specific inflammatory cutaneous lesions of the breasts. First considered by others as a malinger patient, she developed oto-neurological lesions leading to the diagnosis of Wegener's granulomatosis. Five years later, specific antibodies of the disease were present., Conclusion: Cutaneous involvement by ANCA vasculitis can be isolated for a long time. Physicians must have a high degree of suspicion to avoid diagnostic delay of ANCA vasculitis., (Copyright © 2013 Société nationale française de médecine interne (SNFMI). Published by Elsevier SAS. All rights reserved.)

Published
2014
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42. [Chronic cough in a 48-year-old man].

Author

Bélénotti P, Benyamine A, Séguier J, Astoul P, Grandval P, Gaubert JY, Serratrice J, Weiller PJ, Terrier B, and Lachaud A

Subjects
Asthenia diagnosis, Asthenia etiology, Chronic Disease, Cough etiology, Diagnosis, Differential, Humans, Male, Middle Aged, Amyloid Neuropathies, Familial diagnosis, Amyloid Neuropathies, Familial therapy, Cough diagnosis, Cough therapy
Published
2013
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43. [Ischemic cholangitis in intensive care unit: favourable outcome with ursodesoxycholic acid and fenofibrate].

Author

Bélénotti P, Guervilly C, Grandval P, Benyamine A, Ene N, Serratrice J, Petit P, Laugier R, Papazian L, and Weiller PJ

Subjects
Cholagogues and Choleretics administration & dosage, Cholagogues and Choleretics therapeutic use, Fenofibrate therapeutic use, Humans, Hypolipidemic Agents administration & dosage, Hypolipidemic Agents therapeutic use, Intensive Care Units, Male, Middle Aged, Treatment Outcome, Ursodeoxycholic Acid therapeutic use, Cholangitis, Sclerosing drug therapy, Cholangitis, Sclerosing etiology, Critical Care, Fenofibrate administration & dosage, Ursodeoxycholic Acid administration & dosage
Abstract

Introduction: Ischemic cholangitis in intensive care unit is a recently reported liver disease in patients who have had a prolonged mechanical ventilation and vasopressive drug support for multiple organ deficiency. Prognosis is usually poor and the only life-saving therapy is liver transplantation despite ursodesoxycholic acid treatment., Case Report: We report a 63-year-old man who presented with a sclerosis cholangitis after a month in intensive care unit, effectively treated with fenofibrate and ursodesoxycholic acid. Recent reports underline fenofibrate efficacy in the treatment of primary biliary cirrhosis, especially in association with ursodesoxycholic acid. This treatment has prevented liver transplantation for our patient with a correct quality of life., Conclusion: The addition of fibrate to ursodesoxycholic acid improves persistent cholestasis in sclerosing cholangitis., (Copyright © 2012 Société nationale française de médecine interne (SNFMI). Published by Elsevier SAS. All rights reserved.)

Published
2013
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44. [A chronic recurring sharp pain].

Author

Bélénotti P, Sarlon-Bartoli G, Migerel M, Arthuis M, Benyamine A, Ene N, Serratrice J, Weiller PJ, and Delluc A

Subjects
Abdominal Pain etiology, Adult, Angiodysplasia complications, Angiodysplasia etiology, Cachexia etiology, Constriction, Pathologic complications, Constriction, Pathologic diagnosis, Diagnosis, Differential, Diarrhea etiology, Female, Helicobacter Infections complications, Humans, Parenteral Nutrition methods, Plaque, Atherosclerotic complications, Risk Factors, Smoking adverse effects, Stomach Diseases complications, Stomach Ulcer complications, Treatment Outcome, Back Pain etiology, Diarrhea complications, Mesenteric Arteries pathology, Plaque, Atherosclerotic diagnosis, Weight Loss
Published
2012
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45. [Bilateral xerophthalmia in a 60-year-old man].

Author

Bélénotti P, Benyamine A, Bensahla H, Ene N, Sevy A, Attarian S, Serratrice J, Pouget J, Weiller PJ, and Krolak-Salmon P

Subjects
Diagnosis, Differential, Functional Laterality, Humans, Keratoconjunctivitis diagnosis, Male, Middle Aged, Xerophthalmia diagnosis
Published
2010
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