Relevant bibliographies by topics / Jaccoud arthritis

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Academic literature on the topic 'Jaccoud arthritis'

Author: Grafiati
Published: 3 June 2025
Last updated: 20 July 2025

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Journal articles on the topic "Jaccoud arthritis"

1

Loddenkemper, K. "Jaccoud-Arthritis." Zeitschrift für Rheumatologie 58, no. 5 (1999): 289–90. http://dx.doi.org/10.1007/s003930050184.

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2

Stroehmann, A. "Jaccoud-Arthritis beim SLE." Aktuelle Rheumatologie 21, no. 01 (1996): 44. http://dx.doi.org/10.1055/s-2008-1043687.

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3

Ahmadi-Simab, K., P. Lamprecht, and W. L. Gross. "Jaccoud-Arthritis bei systemischem Lupus erythematodes." Zeitschrift für Rheumatologie 64, no. 5 (2005): 343–44. http://dx.doi.org/10.1007/s00393-005-0641-8.

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4

Küçükşahin, Orhan, Nurşen Düzgün, Alexis K. Okoh, and Emre Kulahçioglu. "Response to Rituximab in a Case of Lupus Associated Digital Ischemia." Case Reports in Rheumatology 2014 (2014): 1–4. http://dx.doi.org/10.1155/2014/763608.

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We report the case of a 38-year-old female patient with systemic lupus erythematosus (SLE) and Jaccoud arthritis (JA) that sequentially developed digital ischemic lesions of the hands. In spite of follow-up treatment with glucocorticoids, immunosuppressant, antiaggregant, and potent vasodilatator agents, a serious progression to digital gangrene over a one-month period was observed. Surprisingly, her nonhealing digital lesions improved after two cycles of rituximab (RTX) administration.
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5

Hernández, Martín Annia Daisy, and Noda Ibars Puerto. "Artropatía de Jaccoud en el lupus eritematoso sistémico. Revisión de la literatura a propósito de un caso." Revista Cubana de Reumatología 20, no. 1 (2018): e06. https://doi.org/10.5281/zenodo.1174341.

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<strong>RESUMEN</strong> El Lupus eritematoso sist&eacute;mico es una colagenosis de etiolog&iacute;a a&uacute;n desconocida, que muestra una patogenia de car&aacute;cter multifactorial, aunque con marcada referencia autoinmune; ocasiona afectaci&oacute;n multisist&eacute;mica y presenta un curso cl&iacute;nico variable. Es m&aacute;s frecuente en las mujeres que en los hombres en proporci&oacute;n 8:1 y en determinadas razas; su pico de incidencia se sit&uacute;a entre los 15 y 40 a&ntilde;os de edad. La mayor&iacute;a de los autores describen la afectaci&oacute;n articular del lupus como una
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6

Khaldoun, N., S. Haid, L. Soumia, et al. "AB1340 PREVALENCE OF THE WRISTS AND HANDS SYNOVITIS IN SUBGROUPS OF PATIENTS FOLLOWED FOR SYSTEMIC LUPUS ERYTHEMATOSUS." Annals of the Rheumatic Diseases 81, Suppl 1 (2022): 1776.1–1776. http://dx.doi.org/10.1136/annrheumdis-2022-eular.1481.

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BackgroundJoint damage is one of the most common manifestations of SLE. Represented by the presence of arthralgia or arthritis, with or without deformities or erosions.Musculoskeletal ultrasound allows evaluation of the inflammatory joint damage for more targeted therapeutic approach.ObjectivesThe aim of this study was to estimate the prevalence of the wrists and hands synovitis (WHS) in subgroups of patients with systemic lupus erythematosus (SLE) and to compare them with each other.MethodsOne hundred and sixty-nine patients with SLE were consecutively recruited in the rheumatology unit (cons
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7

Corzo Garcia, P., I. Garcia-Duitama, A. Agustí Claramunt, et al. "AB0486 INFLAMMATORY MUSCULOSKELETAL ABNORMALITIES BY CONTRAST ENHANCED MRI IN SLE PATIENTS." Annals of the Rheumatic Diseases 81, Suppl 1 (2022): 1370.2–1370. http://dx.doi.org/10.1136/annrheumdis-2022-eular.1848.

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BackgroundJoint involvement in SLE is the most frequent manifestation and shows a wide heterogeneity1. It has not a valid classification and it is often underestimated. Subclinical inflammatory musculoskeletal involvement is not well known2.ObjectivesWe aim to describe the prevalence of joint and tendon involvement in hand and wrist of SLE patients, either with clinical arthritis, arthralgia or asymptomatic and compare it with healthy subjects using contrasted MRI.MethodsSLE patients fulfilling SLICC criteria were recruited and classified as follows: group (G) 1: hand/wrist arthritis, G2: hand
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8

Massaro, L., F. Ceccarelli, T. Colasanti, et al. "Anti-carbamylated protein antibodies in systemic lupus erythematosus patients with articular involvement." Lupus 27, no. 1 (2017): 105–11. http://dx.doi.org/10.1177/0961203317713141.

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Objective Several studies have evaluated the prevalence of rheumatoid factor (RF) and anti-citrullinated proteins antibodies (ACPA) in systemic lupus erythematosus (SLE) patients but no data are available on the anti-carbamylated proteins (anti-CarP), a new biomarker for rheumatoid arthritis (RA). We evaluated the anti-CarP prevalence in SLE patients with joint involvement and the associations with different phenotypes. Methods Seventy-eight SLE patients with joint involvement were enrolled (F/M 73/5; mean ± SD age 47.6 ± 11.2 years; mean ± SD disease duration 214.3 ± 115.6 months). As control
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9

Amikishiyev, S., N. Aliyeva, M. Bektas, et al. "AB1299 DIFFERENCES IN THE CLINICAL SPECTRUM OF HAPLOINSUFFICIENCY OF A20 (HA20) CASES DIAGNOSED DURING ADULTHOOD." Annals of the Rheumatic Diseases 81, Suppl 1 (2022): 1756.1–1756. http://dx.doi.org/10.1136/annrheumdis-2022-eular.3269.

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BackgroundHaploinsufficiency of A20 (HA20) is a monogenic autoinflammatory disease caused by heterozygous loss-of-function mutations in TNFAIP3 gene and characterized by Behçet disease (BD)-like manifestations such as mucocutaneous, articular, gastrointestinal, ocular symptoms as well as recurrent fever, elevated acute-phase reactants during relapses; and it usually starts during early childhood. Autoimmunity is another component of HA20 with autoantibodies and variable clinical features resembling systemic lupus erythematosus (SLE) and other autoimmune diseases.ObjectivesWe herein present thr
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10

Cano Garcia, L., J. García-Campos, F. Ortiz-Márquez, A. Reinoso Cobo, L. Ramos Petersen, and J. Marco-Lledó. "POS1191-HPR ULTRASONOGRAPHIC AND FUNCTIONAL CORRELATION OF THE FEET IN PATIENTS WITH SYSTEMIC LUPUS ERYTHEMATOSUS." Annals of the Rheumatic Diseases 82, Suppl 1 (2023): 928.2–929. http://dx.doi.org/10.1136/annrheumdis-2023-eular.3167.

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BackgroundSystemic lupus erythematosus (SLE) is a chronic immune-mediated disease with involvement of various organs[1,2]. El 95% of patients with SLE have musculoskeletal involvement[1], most often in the form of arthralgias or non-erosive arthritis affecting mostly the hands and knees. A subgroup of patients with SLE, which is seen with increasing frequency, late develops a deforming arthropathy as a result of laxity of ligaments and peritendinous apparatus resulting in joint subluxations and tendon ruptures which is part of the accumulated damage of the disease. The foot is a heavily affect
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Conference papers on the topic "Jaccoud arthritis"

1

Leal, Matheus Tozatto Baptista Coelho, Adriane Paz Rocha, Welton Gomes de Paula, Ana Claudia Dias Malta, Joice Rodrigues Rachid Amin, and Rodrigo Braga Pacheco. "JACCOUD S ARTHROPATHY SIMULATING RHEUMATOID ARTHRITIS: THE IMPORTANCE OF DIFFERENTIAL DIAGNOSIS IN THERAPEUTIC CHOICE." In XLI Congresso Brasileiro de Reumatologia. Sociedade Brasileira de Reumatologia, 2024. https://doi.org/10.47660/cbr.2024.1949.

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2

HUBER, MÍRIAM KÜSTER, MARIA BERNADETE RENOLDI DE OLIVEIRA GAVI, LUCAS MARQUES DE AGUIAR FERREIRA, et al. "JACCOUD'S ARTHROPATHY ASSOCIATED WITH PSORIATIC ARTHRITIS." In 36º Congresso Brasileiro de Reumatologia. Editora Blucher, 2019. http://dx.doi.org/10.5151/sbr2019-145.

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