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Journal articles on the topic 'Articular syndrome'

Author: Grafiati

Published: 28 May 2022

Last updated: 31 July 2025

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1

Boric, Igor, Amanda Isaac, Danoob Dalili, Michel Ouchinsky, Michel De Maeseneer, and Maryam Shahabpour. "Imaging of Articular and Extra-articular Sports Injuries of the Hip." Seminars in Musculoskeletal Radiology 23, no. 03 (2019): e17-e36. http://dx.doi.org/10.1055/s-0039-1688696.

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Sports-related articular and periarticular hip injuries are common in athletes. Knowledge of patient complaints and clinical findings are crucial for adequate interpretation of imaging examinations. However, asymptomatic athletes can present abnormal imaging findings, and clinical presentation of hip injuries may be nonspecific. Therefore, a thorough examination of the hip and surrounding soft tissue images is essential.This review describes the intra-articular pathologies encountered in sports activities including labrum or cartilage lesions, associated or not with femoroacetabular hip imping

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2

Shahid, Nayab, Qurba Kiran, Sadia Tariq, et al. "Effects of Elongation Longitudinaux Articular Vertebral and Columnar Decoaption Osteo Articulaire versus Upper Thoracic Mobilization on Forward Head Posture in Upper Cross Syndrome." Healer Journal of Physiotherapy and Rehabilitation Sciences 5, no. 2 (2025): 19–26. https://doi.org/10.55735/hjprs.v5i2.340.

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Background: Upper-crossed syndrome is a common musculoskeletal disorder characterized by forward head posture. Elongation longitudinaux articular vertebral and columnar decoaption osteo articulaire and upper thoracic mobilization are two manual therapy approaches used to address upper cross syndrome, but their comparative effects on forward head posture are unknown. Objective: To compare the effects of elongation longitudinaux articular vertebral and columnar decoaption osteo articulaire and upper thoracic mobilization on forward head posture with upper cross syndrome. Methodology: A randomize

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3

Hamilton, E., and P. Pitt. "Articular manifestations of Scheie's syndrome." Annals of the Rheumatic Diseases 51, no. 4 (1992): 542–43. http://dx.doi.org/10.1136/ard.51.4.542.

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4

Mruthyunjaya, Prakashini, and Manvitha Nadella. "ARTICULAR SYNDROME IN THE ELDERLY: COMMON DIFFERENTIALS AND CHALLENGES." Anti-Aging Eastern Europe 2, no. 3 (2023): 169–75. http://dx.doi.org/10.56543/aaeeu.2023.2.3.07.

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Articular syndrome includes a spectrum of inflammatory and non-inflammatory joint involvement ranging from arthralgia to arthritis. Its phenotype, differentials and management differ slightly in the elderly, considering the added effect of physiological changes with ageing, comorbidity and multimorbidity. This review aims to provide an overview of the common differentials of articular syndrome in the elderly, including the inflammatory and degenerative causes. The common inflammatory arthritis in the elderly includes late-onset rheumatoid arthritis, polymyalgia rheumatica, paraneoplastic arthr

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5

Koles, Sarah, Peter Salat, Andrea Veljkovic, Óliver Marín-Peña, and Ara Kassarjian. "Current Concepts in Extra-articular Impingement of the Hip: Clinical Diagnosis, Imaging, and Treatment." Seminars in Musculoskeletal Radiology 21, no. 05 (2017): 547–60. http://dx.doi.org/10.1055/s-0037-1606140.

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AbstractHip impingement syndromes, particularly femoroacetabular impingement syndrome, have attracted tremendous attention in the past decade. We address some of the less common hip impingement syndromes, mainly the extra-articular hip impingement syndromes. The clinical presentation, imaging, and treatment of anterior, posterior, and lateral hip impingement syndromes are discussed.

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6

Moerman, Rada V., Suzanne Arends, Petra M. Meiners, et al. "Detailed Analysis of the Articular Domain in Patients with Primary Sjögren Syndrome." Journal of Rheumatology 44, no. 3 (2017): 292–96. http://dx.doi.org/10.3899/jrheum.160459.

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Objective.We used the 28-joint Disease Activity Score (DAS28) and the European League Against Rheumatism Sjögren’s Syndrome Disease Activity Index (ESSDAI) articular domain to assess the effect of rituximab (RTX) and abatacept (ABA) on articular involvement in primary Sjögren syndrome (pSS).Methods.Patients with pSS treated with RTX (n = 18) or ABA (n = 13) and having a DAS28 erythrocyte sedimentation rate (ESR)/C-reactive protein (CRP) level ≥ 3.2 at baseline were selected. Generalized estimating equations were used to analyze the DAS28 and ESSDAI articular domain over time.Results.In the RTX

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7

Vashakmadze, Nato D., Mikhail M. Kostik, Nataliya V. Zhurkova, Nataliya V. Buchinskaia, Ekaterina Yu Zakharova, and Margarita A. Soloshenko. "Articular Syndrome Characteristics in Children with Mucopolysaccharidosis Type I." Current Pediatrics 20, no. 6s (2021): 567–75. http://dx.doi.org/10.15690/vsp.v20i6s.2364.

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Background. Mucopolysaccharidosis type I is disease from the group of lysosomal storage disease developing due to mutations in the IDUA gene. It leads to the accumulation of glycosaminoglycans (GAGs) in organs and tissues. Joints damage in this disease is systemic and progressive.Objective. The aim of the study. Nowadays, relevant issue is to investigate the effects of various types of pathogenetic therapy on the state of the osteoarticular system in patients with severe and mild phenotypes of MPS I to prevent further progression of joint pathology.Methods. The study included 46 patients diagn

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8

Leys, Christophe, Catherine Eschard, Jacques Motte, Anne-Marie Prieur, Bernard Kalis, and Philippe Bernard. "Chronic Infantile Neurological, Cutaneous, and Articular Syndrome with Severe Early Articular Manifestations." Pediatric Dermatology 22, no. 3 (2005): 222–26. http://dx.doi.org/10.1111/j.1525-1470.2005.22316.x.

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9

Hutchlngs, C. J., M. C. Hillarby, M. J. Mcmahon, W. E. R. Ollier, and D. M. Grennan. "HLA-DPAI aND HLA-DPBl in Rheumatoid Arthritis And Its Subsets." Disease Markers 11, no. 1 (1993): 37–44. http://dx.doi.org/10.1155/1993/583825.

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The aim of this study was to examine the relationship between HLA-DP and susceptibility to articular and extra-articular features (Felty's syndrome and vasculitis) of rheumatoid arthritis (RA). The possible association of DP types with severity of articular disease was also analysed. No statistically significant associations were observed between HLA-DP alleles and articular or extra-articular features of RA, or to the severity of the arthritis when p was corrected for the number of alleles tested.

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10

IWAMOTO, NAOKI, ATSUSHI KAWAKAMI, MAMI TAMAI, et al. "Determination of the Subset of Sjögren’s Syndrome with Articular Manifestations by Anticyclic Citrullinated Peptide Antibodies." Journal of Rheumatology 36, no. 1 (2009): 113–15. http://dx.doi.org/10.3899/jrheum.080193.

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Objective.To investigate whether anticyclic citrullinated peptide antibodies (anti-CCP) predict the subset of Japanese patients with Sjögren’s syndrome (SS) with articular manifestations.Methods.Eighty-seven patients with SS were enrolled. Prevalence of anti-CCP antibodies, IgM rheumatoid factor, anti-Ro/SSA antibody, anti-La/SSB antibody, and serum IgG concentration and their relation to articular manifestations were examined. Articular manifestations included morning stiffness and the presence of tender or swollen joints.Results.Eighty-seven SS patients were divided into 3 groups: 14 seconda

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11

Malyshenko, O. S., T. A. Raskina, Yu V. Averkieva, T. V. Protasova, and A. M. Dubaeva. "Articular syndrome in an HIV-infected patient." Modern Rheumatology Journal 14, no. 4 (2020): 161–64. http://dx.doi.org/10.14412/1996-7012-2020-4-161-164.

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Nowadays, HIV infection is one of the leading health problems. Its clinical signs are extremely diverse and are associated with many diseases, including rheumatic diseases. This paper describes the course of articular syndrome in a patient with HIV infection. In the patient given, asymmetric arthritis of the left wrist, first metacarpophalangeal, and knee joints with no damage to the skin and mucous membranes or enthesitis, a negative HLA-B27 test, and the whole clinical picture, as well as no convincing evidence of rheumatic diseases might suggest the presence of arthritis associated with HIV

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12

Sayakbekov, K., G. Saatova, and G. Maimerova. "Clinical Features of Reiter’s Syndrome in Children." Bulletin of Science and Practice 6, no. 5 (2020): 137–46. http://dx.doi.org/10.33619/2414-2948/54/17.

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The clinical features of articular syndrome and extra-articular manifestations in children with Reiter’s syndrome (illness) were studied. Reiter’s syndrome in childhood has some features of the course and development of the disease. In childhood, asymmetry of lesions of the joints of the lower extremities with early involvement of small feet joints in the process, possible flushing of the skin over the affected joints, intense pain, rare involvement in the process of the hip joints, lumbar spine and unilateral sacroiliitis is characteristic. Extraarticular manifestations proceeded often erased

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13

Povzun, A. S., V. I. Mazurov, E. V. Shchemeleva, K. A. Povzun, E. Yu Kovalchuk та V. A. Kostenko. "Prevalence of аcute articular syndrome. Literature review and own data". EMERGENCY MEDICAL CARE 23, № 4 (2022): 61–73. http://dx.doi.org/10.24884/2072-6716-2022-23-4-61-73.

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The study of the occurrence of articular syndrome in general, and acute articular syndrome (AAS) in particular, is an important medical and social task, the solution of which makes it possible to determine the amount of necessary forces and means for the organization of medical care for these patients. Since 2008, the authors have been studying the features of diagnosis and treatment of patients with AAS, for the first time in the Russian Federation on the basis of the St. Petersburg Research Institute of Emergency Medicine named after I. I. Dzhanelidze introduced the concept of providing medi

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14

Roy, Daniel F., Jean Fleury, Suzanne B. Fontaine, and Robert G. Dussault. "Clinical Evaluation of Cervical Facet Joint Infiltration." Canadian Association of Radiologists Journal 39, no. 2 (1988): 118–20. https://doi.org/10.1177/084653718803900209.

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Twenty-one patients with cervical facet syndrome underwent 39 facet joint infiltrations with corticosteroids using fluoroscopie guidance. There were 22 intra-articular and 17 peri-articular injections. This treatment relieved symptoms in 91% of patients. Follow-up ranged from one week to 12 months. However, symptoms usually recurred, specifically in 71% of patients with complete responses and in 42% of those with partial relief. There was no significant difference in response between patients receiving intra-articular or peri-articular injections (χ 2 = 2.283).

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15

Kidanu, Debora, Emma Rowbotham, Andrew J. Grainger, Philip Robinson, and William S. Bolton. "Greater trochanteric pain syndrome." InnovAiT: Education and inspiration for general practice 10, no. 1 (2016): 39–44. http://dx.doi.org/10.1177/1755738016678645.

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Greater trochanteric pain syndrome (GTPS) is a common problem that is both debilitating and challenging to manage. In the past, the terms GTPS and greater trochanteric bursitis were used interchangeably, however, inflammation is not always a feature, and in fact, overuse or injury of the gluteal muscles may be the predominant feature. GTPS is now understood to involve multiple pathologies that affect the intra-articular or peri-articular spaces of the hip. Early detection and management of GTPS by GPs can improve patients’ quality of life. Currently, the use of corticosteroid injection therapy

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16

Iaremenko, O. B., and D. I. Koliadenko. "HIV-ASSOCIATED ARTHRITIS. Review and clinical cases." Medical Science of Ukraine (MSU) 18, no. 1 (2022): 73–83. http://dx.doi.org/10.32345/2664-4738.1.2022.10.

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Relevance. HIV infection is characterized by a wide spectrum of clinical manifestations, including musculoskeletal symptoms, which can occur at any stage of the disease. Objective: to analyze own clinical cases with rheumatologic manifestations of HIV infection in context of literature data on the spectrum of musculoskeletal manifestations of HIV infection, approaches to diagnosis and treatment. Methods. Presentation of own clinical cases and review of scientific publications in the international electronic scientometric database PubMed using keywords «HIV infection», «arthritis»,

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17

Kamyshnikova, L. A., D. S. Pisankina, A. N. Payudis, Yu S. Pavlova, and O. A. Bolkhovitina. "Post-COVID musculo-articular syndrome and COVID-19 association with rheumatoid arthritis." Ural Medical Journal 22, no. 1 (2023): 104–10. http://dx.doi.org/10.52420/2071-5943-2023-22-1-104-110.

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Introduction. Since the COVID-19 pandemic, there has been a great deal of evidence for a variety of post-COVID symptoms, including the presence of a musculo-articular syndrome. The aim of the study was to analyze the current literature data on the prevalence of musculo-articular syndrome and to study the association of coronavirus infection with the development of rheumatoid arthritis. Materials and methods. We searched PubMed, Medline, and Google Scholar (2020-2022) for articles using the following keywords: post-covid syndrome, muscular articular syndrome or muscle and joint pain, COVID-19,

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18

Strongin, L. G., K. D. Klimova, E. A. Grunina, K. G. Korneva, and E. S. Trifonova. "Clinical and metabolic aspects of the influence of type 2 diabetes mellitus on the manifestation of articular syndrome in patients with gonarthrosis." Problems of Endocrinology 57, no. 4 (2011): 17–20. http://dx.doi.org/10.14341/probl201157417-20.

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The present work was designed to study the influence of type 2 diabetes mellitus on the clinical course of articular syndrome in patients with combined pathology. A total of 45 patients with diabetes mellitus and gonarthrosis were examined and 45 ones with gonarthrosis without concomitant type 2 diabetes. The patients of both groups were matched for age, sex, duration and stage of gonarthrosis, and body mass index. It was shown that concomitant diabetes mellitus promotes progression of articular syndrome. Decompensation of diabetic state leads to exacerbation of pain syndrome, marked functiona

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19

Bakutenko, I. Y., I. D. Haurylchyk, E. V. Sechko, A. M. Tchitchko, A. V. Sukalo, and N. I. Ryabokon. "Polymorphic variants of proteasomal genes PSMA3 and PSMA6 in children with articular syndrome and juvenile idiopathic arthritis." Doklady of the National Academy of Sciences of Belarus 65, no. 4 (2021): 466–73. http://dx.doi.org/10.29235/1561-8323-2021-65-4-466-473.

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A comparative analysis of three single nucleotide variations of the proteasomal genes PSMA3 (rs2348071) and PSMA6 (rs2277460 and rs1048990) was carried out in the groups of children from 1 to 16 years old with the autoimmune rheumatic disease - juvenile idiopathic arthritis (JIA; n = 199), with articular syndrome of non-autoimmune etiology (n = 229) and in the clinical control group with neither autoimmune nor chronic inflammatory diseases (n = 379). PCR, PCR–RFLP and real-time PCR were used for genotyping. It was found that the CG genotype and G allele of rs10489990 polymorphism (OR = = 1.93;

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20

Gorbunova, Dar'ja Yu, Zinaida A. Morgunova, and Oleg M. Uryasyev. "Clinical and laboratory peculiarities of combined clinical course of metabolic and articular syndromes." I.P. Pavlov Russian Medical Biological Herald 26, no. 2 (2018): 229–37. http://dx.doi.org/10.23888/pavlovj20182229-237.

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Aim. To identify clinical and laboratory peculiarities of a combined clinical course of metabolic and articular syndromes. Materials and Methods. In the research 126 individuals participated. They were arranged into 3 groups: the 1st group included 46 patients with comorbid pathology, the 2nd group – 44 patients with metabolic syndrome, and the 3d group – 36 patients with articular syndrome. The following parameters were evaluated: anthropometric data (height, body mass, body mass index, waist circumference), lipid spectrum, glycohemoglobin, nonspecific markers of inflammation, daily pro

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Gorbunova, Dar'ja Yu, Zinaida A. Morgunova, and Oleg M. Uryasyev. "Clinical and laboratory peculiarities of combined clinical course of metabolic and articular syndromes." I.P. Pavlov Russian Medical Biological Herald 26, no. 2 (2018): 229–37. http://dx.doi.org/10.23888/pavlovj2018262229-237.

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Aim. To identify clinical and laboratory peculiarities of a combined clinical course of metabolic and articular syndromes. Materials and Methods. In the research 126 individuals participated. They were arranged into 3 groups: the 1st group included 46 patients with comorbid pathology, the 2nd group – 44 patients with metabolic syndrome, and the 3d group – 36 patients with articular syndrome. The following parameters were evaluated: anthropometric data (height, body mass, body mass index, waist circumference), lipid spectrum, glycohemoglobin, nonspecific markers of inflammation, daily pro

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22

Gallego, Maribel, Catalina Jaramillo, Jaime Sierra, and Margarita María Velásquez. "Criopirinopatías: ¿qué son?, ¿cómo detectarlas? y ¿cuál es el enfoque de su tratamiento?" Revista de la Asociación Colombiana de Dermatología y Cirugía Dermatológica 27, no. 2 (2019): 108–27. http://dx.doi.org/10.29176/2590843x.983.

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Los síndromes periódicos asociados con criopirinas (Cryopyrin Associated Periodic Syndromes, CAPS), o criopirinopatías, son enfermedades raras que hacen parte de los síndromes autoinflamatorios, caracterizados por episodios de fiebre recurrente e inflamación sin etiología autoinmunitaria, neoplásica ni infecciosa. Entre estos síndromes, los CAPS incluyen tres entidades: el síndrome autoinflamatorio familiar por frío (Familial Cold Autoinflammatory Syndrome, FCAS), el síndrome de Muckle-Wells y la enfermedad multisistémica inflamatoria de inicio neonatal (Neonatal Onset Multisystem Inflammator

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23

Abel, Frederik, Florian Schmaranzer, and Reto Sutter. "Sports-related Hip Injuries." Seminars in Musculoskeletal Radiology 29, no. 03 (2025): 442–56. https://doi.org/10.1055/s-0045-1805079.

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AbstractSports-related injuries of the hip joint and surrounding structures are frequently encountered in athletes, encompassing a wide spectrum of osseous, intra-articular, and extra-articular pathologies. Early and accurate detection of typical injury patterns across various sports can expedite recovery. Delayed diagnosis often leads to prolonged return to play and progression of low grade to more severe injuries. These injuries, caused by repetitive stress or acute trauma, include fractures, hip dislocations, and intra-articular abnormalities, such as femoroacetabular impingement, labral te

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24

Kim, Ji Hyoun, You-Jung Ha, Eun Ha Kang, Yeong Wook Song, and Yun Jong Lee. "Case of Idiopathic Hypereosinophilic Syndrome with Articular Involvement." Journal of Rheumatic Diseases 25, no. 3 (2018): 207. http://dx.doi.org/10.4078/jrd.2018.25.3.207.

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25

Misaggi, B., M. Gallazzi, M. Colombo, and M. Ferraro. "Articular facets syndrome: diagnostic grading and treatment options." European Spine Journal 18, S1 (2009): 49–51. http://dx.doi.org/10.1007/s00586-009-0987-8.

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26

MISHRA, M. B., P. RYAN, P. ATKINSON, et al. "EXTRA-ARTICULAR FEATURES OF BENIGN JOINT HYPERMOBILITY SYNDROME." Rheumatology 35, no. 9 (1996): 861–66. http://dx.doi.org/10.1093/rheumatology/35.9.861.

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27

Pouchot, Jacques. "Painful Articular Syndrome and Human Immunodeficiency Virus Infection." Archives of Internal Medicine 152, no. 3 (1992): 646. http://dx.doi.org/10.1001/archinte.1992.00400150146029.

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Pouchot, J. "Painful articular syndrome and human immunodeficiency virus infection." Archives of Internal Medicine 152, no. 3 (1992): 646. http://dx.doi.org/10.1001/archinte.152.3.646.

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29

Yasuda, T., H. D. Nah, J. Laurita, et al. "Muenke Syndrome Mutation, FgfR3P244R, Causes TMJ Defects." Journal of Dental Research 91, no. 7 (2012): 683–89. http://dx.doi.org/10.1177/0022034512449170.

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Muenke syndrome is characterized by various craniofacial deformities and is caused by an autosomal-dominant activating mutation in fibroblast growth factor receptor 3 ( FGFR3P250R). Here, using mice carrying a corresponding mutation ( FgfR3P244R), we determined whether the mutation affects temporomandibular joint (TMJ) development and growth. In situ hybridization showed that FgfR3 was expressed in condylar chondroprogenitors and maturing chondrocytes that also expressed the Indian hedgehog (Ihh) receptor and transcriptional target Patched 1( Ptch1). In FgfR3P244R mutants, the condyles display

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30

Velasco-Benitez, Carlos Alberto, Cara Axelrod, Ana C. Falcon, Lilibet Fernadez Valdes, and Miguel Saps. "Prevalence of joint hypermobility, postural orthostatic tachycardia syndrome (POTS), and orthostatic hypotension in school-children." Andes Pediatrica 93, no. 1 (2022): 53. http://dx.doi.org/10.32641/andespediatr.v93i1.3755.

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Los niños con hipermovilidad articular, síndrome de taquicardia ortostática postural e hipotensión ortostática presentan síntomas autonómicos como mareos, náuseas, dolores de cabeza y palpitaciones. Se desconoce si existe una relación fisiopatológica entre los trastornos del tejido conectivo y los síntomas autonómicos. No hay datos publicados sobre la prevalencia de los trastornos a nivel comunitario. Objetivo primario: Evaluar la prevalencia de la hipermovilidad articular, la hipotensión ortostática y el síndrome de taquicardia ortostática postural en niños. Objetivo secundario: Determinar la

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31

Kopelev, Alexander A., Margarita A. Gromova, and Julia B. Chervyakova. "Yersiniosis with a predominance of articular syndrome: challenges of outpatient admission. Clinical case." Clinical review for general practice 2, no. 5 (2021): 35–38. http://dx.doi.org/10.47407/kr2021.2.5.00069.

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The articular syndrome, although it requires, first of all, the exclusion of systemic diseases of the connective tissue, contrary to the common stereotype, is rather nonspecific. It can also be accompanied by infectious pathology, the incidence of various variants of which is quite high. On an outpatient basis, doctors of any specialty are faced with yersiniosis, the clinical manifestations of which are polymorphic and similar to those of other diseases. Below is an example of the course of yersiniosis with a predominance of articular syndrome in the clinical picture.

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Zaynutdinova, G. H., A. E. Babushkin, and N. A. Nikitin. "Chauffard-Still syndrome (clinical case)." POINT OF VIEW. EAST – WEST, no. 4 (November 2, 2021): 74–76. http://dx.doi.org/10.25276/2410-1257-2021-4-74-76.

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The article presents a clinical case of Chauffard-Still syndrome. It is shown that for the correct etiological diagnosis of iridocyclitis in Still's syndrome, careful collection of anamnesis, the connection of the articular syndrome with uveitis and characteristic ophthalmological changes in the form of ribbon-like dystrophy of the cornea are important. Key words: Chaufard-Still syndrome, uveitis, corneal ribbon dystrophy.

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Griffiths, H. J., and P. Virtama. "Juxta-Articular Erosions in Reflex Sympathetic Dystrophy." Acta Radiologica 29, no. 2 (1988): 183–87. http://dx.doi.org/10.1177/028418518802900209.

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Thirty-one patients with documented reflex sympathetic dystrophy syndrome (RSDS) were reviewed for their radiographic changes. Juxta-articular and metaphyseal bone loss was found in the majority of the patients. Juxta-articular bone loss closely resembling erosions seen in rheumatoid arthritis was found in all the patients. The significance of these findings is discussed.

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Zhdan, V. M., H. V. Volchenko, M. Yu Babanina, M. V. Tkachenko, and O. V. Gordienko. "CARDIORENAL SYNDROME AS EXTRA-ARTICULAR MANIFESTATION OF RHEUMATOID ARTHRITIS." Актуальні проблеми сучасної медицини: Вісник Української медичної стоматологічної академії 22, no. 3-4 (2022): 237–40. http://dx.doi.org/10.31718/2077-1096.22.3.4.237.

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The article provides a description of a complex clinical case of cardiorenal syndrome type II in a patient having rheumatoid arthritis and a high degree of activity. The aim of this work is to highlight the problem of multiple organ damage in severe autoimmune diseases, as well as to share the experience of diagnostic and therapeutic approaches in such situations. Under a long-term articular syndrome, the patient subacutely develops new threatening symptoms: signs of inflammatory cardiomyopathy, heart failure, nephropathy, acute renal failure. But thanks to intensive anti-inflammatory therapy,

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Васильева, L. Vasileva, Лахин, and D. Lakhin. "The Clinical Efficacy of Combined Use of the Metformin and the Atorvastatin in Patients with Osteoarthritis and Metabolic Syndrome." Journal of New Medical Technologies 22, no. 3 (2015): 93–98. http://dx.doi.org/10.12737/13307.

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The purpose was to evaluate the effectiveness of combined use of the Metformin and the Atorvastatin for the correction of the metabolic syndrome in patients with osteoarthritis. The study included 70 patients with osteoarthri-tis and metabolic syndrome, who were divided into 2 groups: control and basic. In the control group, the patients received only pathogenetic treatment of osteoarthritis and anti-hypertensive therapy. Patients of the main group also received the Metformin 500 mg x 2 times and the Atorvastatin 10 mg/day. The authors monitored biochemical, anthropo-metric indicators, assesse

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Hilal, H., O. Soussi, H. Arbouni, et al. "Teno-Synovial Chondromatosis: A Radiological Case Report with Review of the Literature." Scholars Journal of Medical Case Reports 10, no. 7 (2022): 684–86. http://dx.doi.org/10.36347/sjmcr.2022.v10i07.020.

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Teno-synovial chondromatosis is an extra-articular cartilaginous or osteo-cartilaginous multinodular proliferation by metaplasia of synovial tissue. It can be primary (Reichel-Jones-Henderson syndrome) or secondary (trauma, arthritis, neuro-arthropathy...). We report the case of an extra-articular teno-synovial osteochondromatosis of the flexors of the 3rd finger by reviewing the different data in the literature.

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Romero Galván, Edison Edgardo. "Cervical degenerative espondilopathy in post-menopausal women." Obstetrics & Gynecology International Journal 15, no. 2 (2024): 59–64. http://dx.doi.org/10.15406/ogij.2024.15.00735.

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Cervical syndromes comprise a set of clinical conditions that have pain (cervicalgia) in common, to which are added muscular, articular, neurological and even vascular manifestations, with cephalic (cervical cephalic syndrome) and brachial (cervical brachialgic syndrome) irradiations, whose The origin is degenerative spondylodiscopathy or cervical spondylosis. It is a very common entity with an incidence of 85% in people over 60 years of age and onset at an early age, with a high incidence in women. The most common etiology is degenerative: spondylo-disc-uncus-arthrosis constituting 90% of cas

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Chafa, O., A. M. Fischer, F. Meriane, et al. "Behçet Syndrome Associated with Protein S Deficiency." Thrombosis and Haemostasis 67, no. 01 (1992): 001–3. http://dx.doi.org/10.1055/s-0038-1648128.

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SummaryBeçget syndrome is a multisystem disorder characterized by ocular, mucocutaneous, articular, gastrointestinal and neurologic abnormalities. We report here an unusual case of Beçget syndrome, characterized by the importance of the thrombotic events(7 phlebitis of both legs and resection of two toes). Additional manifestations of the Beçget syndrome occurred only 10 years after the first thrombotic episode. The oldest daugther of the propositus and his brother suffered also from thrombophlebitis; this familial history of thrombosis led to the performance of a haemostatic study. A congenit

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Bruzzese, V., C. Marrese, P. Scolieri, and J. Pepe. "Psoriatic spondyloarthritis and Sjögren syndrome: a casual association?" Reumatismo 72, no. 3 (2020): 170–72. http://dx.doi.org/10.4081/reumatismo.2020.1287.

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The association between Sjögren syndrome (SS) and psoriatic arthritis (PsA) is rare. Herein, we report a case of SS in a PsA patient with the mutilans variant. A 67-year old woman developed PsA with progressive articular destruction up to the typical deformation of ‘telescoping fingers’ in the distal phalanges. Psoriatic onychopathy presented ten years after the osteolytic damage in the hands. This late appearance led to delayed diagnosis and therapy, and, consequently, worsened the articular destruction. Thereafter, the patient developed a typical SS with clinical symptoms, such as xerophthal

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Buranova S.N. "Retrospective Evaluation Of Joint Syndrome And Joint Disorders In Osteoarthritis." Texas Journal of Medical Science 39 (December 24, 2024): 65–70. https://doi.org/10.62480/tjms.2024.vol39.pp65-70.

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Retrospective assessment of clinical signs and course of the disease in patients with osteoarthritis in the sex ratio. Materials and Methods: In this scientific study, a retrospective analysis of 300 patients hospitalized in the City Clinical Hospital No. 3 from 2015 to 2019 was carried out based on medical records, with an emphasis on the analysis of the clinical course and consequences of the disease. Results: On the basis of the obtained data on x-ray images, the articular syndrome and joint structure disorders observed in patients with osteoarthritis (OA) were assessed. Conclusions: It was

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Witke-Woźniak, Agnieszka, Michał Wychowański, Tomasz Dąmbski, Karina Szymfel, and Tomasz Kochański. "Hip muscle strength and static balance in patients with snapping hip syndrome – a pilot study." Advances in Rehabilitation 30, no. 3 (2016): 55–68. http://dx.doi.org/10.1515/rehab-2015-0049.

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Abstract Introduction: Snapping hip syndrome (SHS) occurs in 5-10% of the global population. A back and forth skip of the tendon of the dysfunctional muscle across the osseous prominence is the most common symptom of this condition. Mainly young generation suffers from SHS. Depending on the structures that cause an audible snap, snapping hip syndrome may be classified into intra-articular and extra-articular types. The main aim of the research was to assess the strength of the major hip muscles and static balance in patients with snapping hip syndrome. Material and methods: The research was ca

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Plahotnikova, Svetlana V., Galina V. Santalova, and Galina Yu Poretskova. "Leukemia in a child under the guise of juvenile arthritis." Russian Pediatric Journal 26, no. 4 (2023): 296–99. http://dx.doi.org/10.46563/1560-9561-2023-26-4-296-299.

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A clinical case of diagnosis of the onset of leukemia in an 8-year-old child, began with a bone-joint syndrome and was the only one at the beginning of the disease, is presented. This made it much more difficult to make a timely diagnosis. In addition to the severity of the articular syndrome at the onset of the disease, polymorphism of primary clinical manifestations was the reason for the  examination of the child in children’s departments of various profiles. The diagnostic search took 4 months, since laboratory changes  in the patient were observed later than clinical symptoms.

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García-Germán, Diego, Segundo Sánchez-Gutiérrez, Ángel Bueno, et al. "Intra-articular osteoid osteoma simulating a painful fabella syndrome." Knee 17, no. 4 (2010): 310–12. http://dx.doi.org/10.1016/j.knee.2010.02.008.

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McKinney, Christopher, Nirupma Sharma, and Rita S. Jerath. "Livedoid Dermatitis (Nicolau Syndrome) Following Intra-Articular Glucocorticoid Injection." JCR: Journal of Clinical Rheumatology 20, no. 6 (2014): 339–40. http://dx.doi.org/10.1097/rhu.0000000000000146.

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Sharma, H., B. Rana, and M. Naik. "Bipedal compartment syndrome following bilateral intra-articular calcaneal fractures." Foot and Ankle Surgery 10, no. 2 (2004): 93–96. http://dx.doi.org/10.1016/j.fas.2004.01.004.

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Desinova, O., M. Starovoytova, A. Khelkovskaia-Sergeeva, et al. "AB0733 Musculo-articular syndrome in patients with Systemic Sclerosis-polymyositis/dermatomyositis overlap syndrome." Annals of the Rheumatic Diseases 81, Suppl 1 (2022): 1493.2–1493. http://dx.doi.org/10.1136/annrheumdis-2022-eular.4759.

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BackgroundSystemic Sclerosis-polymyositis/dermatomyositis overlap syndrome (SSc-PM/DM) occurs in 10 to 37% of cases and has great differential diagnostic difficulties. Muscle damage in SSc-PM/DM is represented by myositis with primary inflammatory and necrotic alterations in muscle fibers by type of PM/DM.ObjectivesTo evaluate joint and muscle damage in patients with SSc-PM/DM.Methods112 pts had idiopathic inflammatory myopathies, of which 73 pts with SSc-PM/DM (51 pts with lSSc and 22 pts with dSSc, male/female 24/49, mean age 44±14,5 years, average disease’s duration 7 (2;9) years) had the s

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Mehra, Simmi. "A Variant Articular Facet on Left Second Rib." Journal of Mahatma Gandhi University of Medical Sciences and Technology 2, no. 1 (2017): 29–30. http://dx.doi.org/10.5005/jp-journals-10057-0027.

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ABSTRACT During routine scanning of bones in the Department of Anatomy, Mahatma Gandhi Medical College & Hospital, Jaipur, India, an unusual second rib belonging to left side was found having an oval facet, almost centrally placed along the inner border of the shaft. In the absence of the corresponding skeleton, it can be hypothesized that the left first rib or an extra rib articulated with the second rib at this facet. Such structural anomalies of ribs are quite rare and need to be documented. If present, they may lead to compression of neurovascular structures crossing the ribs leading t

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Bechakh, Islam. "Syndrome de Stickler : une observation clinique." Annales Africaines de Medecine 15, no. 2 (2022): e4626-e4628. http://dx.doi.org/10.4314/aamed.v15i2.13.

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Stickler syndrome, also known as hereditary arthroophtalmopathy, is a dominantly inherited polymarformative syndrome characterized by clinical signs as follows: i) polyepiphyseal dysplasia that can lead to early arthrosis, ii) bilateral myopia that is not very progressive but can lead to retinal detachment, and iii) facial dysmorphia that may improve with age. This syndrome may include severe orofacial abnormalities such as Pierre Robin syndrome. We report the case of a 14-year-old child diagnosed with an incomplete form of the syndrome but who fulfilled the diagnostic criteria of this syndrom

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Aleksanyan, K., S. Chebysheva, A. Meleshkina, E. Popova, and E. Zholobova. "AB0999 HALLMARK CLINICAL FEATURES of JUVENILE PSORIATIC ARTHRITIS (JPSA)." Annals of the Rheumatic Diseases 79, Suppl 1 (2020): 1792.1–1793. http://dx.doi.org/10.1136/annrheumdis-2020-eular.1275.

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Background:JPsA is presented in 4 to 9% children with juvenile arthritis [1,2]. According to ILAR criteria, patients with uveitis, HLA-B27-positivity, and other exclusion criteria cannot be included in the JPsA category. Therefore, in pediatric rheumatological practice, the Vancouver criteria are more often used [3].Objectives:to identify clinical features of psoriatic arthritis in children.Methods:a single center, prospective and retrospective, continuous clinical trial for the period from 1989 to 2019 was conducted.Results:We observed 83 patients with JPsA aged from 4 months to 17 years. Fif

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Iman, Kazi, Laboni Akter, Kamrul Laila, Mohammad Imnul Islam, and Shahana Akhter Rahman. "Atypical Dermatological Presentation of Multisystem Inflammatory Syndrome in a Child with Polyarticular JIA: A Case Report." Bangladesh Journal of Child Health 46, no. 2 (2024): 86–88. http://dx.doi.org/10.3329/bjch.v46i2.72122.

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Multisystem inflammatory syndrome in children (MIS-C) is an inflammatory process that occurs after infection with SARS-CoV-2 virus. In this syndrome children usually present with fever, rash, abdominal pain, diarrhea or vomiting, hypotension and shock. Children may need urgent care if heart, blood vessels or other vital organs are involved. Poly-articular Juvenile Idiopathic arthritis is a subset of JIA defined by presence of arthritis of five or more joints within 6 months of disease onset along with other criteria of JIA. In this case report we report mucocutaneous manifestation of MIS-C in

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