Osteonekrosen bei Morbus Adamantiades-Beh�et: Diagnostik, Therapie und Verlauf

Jäger, Markus; Thorey, Fritz; Wild, Alexander; Voede, Mark; Krauspe, Rüdiger

doi:10.1007/s00393-003-0473-3

Cited by 8 publications

(3 citation statements)

References 12 publications

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“…Few cases of necrotizing myositis in BS have been reported (100), an both focal and generalized manifestations have been described. Osteonecrosis is rarely observed in patients with BS and could be corticosteroid-associated in a significant proportion of cases described (101).…”

Section: Further Locomotor Involvementmentioning

confidence: 96%

Behçet‘s Syndrome Apart From the Triple Symptom Complex: Vascular, Neurologic, Gastrointestinal, and Musculoskeletal Manifestations. A Mini Review

Kötter

Lötscher

2021

Front. Med.

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Behçet‘s Syndrome (BS) is a variable vessel vasculitis according to the Chapel Hill Consensus Nomenclature (1) and may thus affect any organ, including major and minor arterial and venous vessels to a varying degree and with varying frequency. Although the main features of BS are recurrent oral and genital aphthous ulcers, cutaneous lesions, ocular inflammation and arthritis—major vessel and life—or organ threatening involvement of internal organs and the central and peripheral nervous system occur. In general, BS in Europe appears to form six phenotypes of clinical manifestations (2), which are (1) mucocutaneous only, (2) predominant arthritis/articular involvement, (3) vascular phenotype, (4) ocular manifestations, which are most likely associated with CNS manifestations and HLA-B51, (5) dominant parenchymal CNS manifestations (being associated with the ocular ones), and (6) gastrointestinal involvement. Mucocutaneous manifestations are present in almost all patients/all phenotypes. In the following review, we summarize the current knowledge concerning vascular, neurologic, gastrointestinal and musculoskeletal manifestations of the disease.

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Section: Further Locomotor Involvementmentioning

confidence: 96%

Behçet‘s Syndrome Apart From the Triple Symptom Complex: Vascular, Neurologic, Gastrointestinal, and Musculoskeletal Manifestations. A Mini Review

Kötter

Lötscher

2021

Front. Med.

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“…Но в других исследованиях отсутствовала корреляция между наличием АКЛ и развитием АН (в том числе у больных СКВ), ввиду чего АФА и АФС считаются спорными факторами риска развития АН [65,72,73]. При васкулитах описаны единичные случаи развития АН [74][75][76], и авторы связывают их с терапией ГК.…”

Section: таблица 1 эпидемиология аваскулярного некроза в миреunclassified

Avascular necrosis of bone tissue: Definition, epidemiology, types, risk factors, pathogenesis of the disease. Analytical review of the literature

Bialik¹,

Макаров²,

Bialik

et al. 2023

Naučno-praktičeskaâ revmatologiâ

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Avascular necrosis (AN) of bone tissue is a common pathology that affects people of any age, more often young and able-bodied. The disease leads to rapid destruction of the subchondral bone and collapse, followed by the development of secondary osteoarthritis (OA) of the affected joint.The purpose of this review article is to present the accumulated knowledge about the prevalence of AN, the most commonly affected joints, risk factors and pathogenesis of the disease. Since most of the world’s literature sources present knowledge about the individual parts and facts that make up the pathogenesis of AN, this article analyzes all known paths of the development of the disease from the onset of ischemia to collapse and the development of secondary OA and the pathogenesis is presented in chronological order. Based on the results of the article, a definition of the term AN was proposed, and the stages of the disease within the pathogenesis, the most promising for conservative methods of treatment, were identified.

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“…Arthritis and arthralgia are the commonest rheumatologic findings in BD. However, rare musculoskeletal findings including osteonecrosis, myalgia, and fibromyalgia may also be associated with BD [20–22]. Findings relevant to bone metabolism is lacking.…”

Section: Bone Metabolismmentioning

confidence: 99%

Musculoskeletal Findings in Behcet's Disease

Biçer

2012

Pathology Research International

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Behcet's disease is a multisystem disease characterized by recurrent oral and genital ulcers, relapsing uveitis, mucocutaneous, articular, gastrointestinal, neurologic, and vascular manifestations. Rheumatologic manifestations may also occur in Behcet's disease, and arthritis and arthralgia are the most common musculoskeletal findings followed by enthesopathy, avascular necrosis, myalgia, and myositis. Although the main pathology of Behcet's disease has been known to be the underlying vasculitis, the etiology and exact pathogenesis of the disease are still unclear. Musculoskeletal findings of Behcet's disease, the relationship between Behcet's disease and spondyloarthropathy disease complex, and the status of bone metabolism in patients with Behcet's disease were discussed in this paper.

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Osteonekrosen bei Morbus Adamantiades-Beh�et: Diagnostik, Therapie und Verlauf

Cited by 8 publications

References 12 publications

Behçet‘s Syndrome Apart From the Triple Symptom Complex: Vascular, Neurologic, Gastrointestinal, and Musculoskeletal Manifestations. A Mini Review

Behçet‘s Syndrome Apart From the Triple Symptom Complex: Vascular, Neurologic, Gastrointestinal, and Musculoskeletal Manifestations. A Mini Review

Avascular necrosis of bone tissue: Definition, epidemiology, types, risk factors, pathogenesis of the disease. Analytical review of the literature

Musculoskeletal Findings in Behcet's Disease

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