Identificación de sitios ideales para el estudio histopatológico de la tarsitis en pacientes con espondiloartropatías

González, Rebeca Ramírez; Abraham, María Virgilia Soto; Viteli, Antonio Ugalde; Pacheco‐Tena, César; Burgos‐Vargas, Rubén

doi:10.1016/s1699-258x(06)73041-8

Cited by 2 publications

(2 citation statements)

References 8 publications

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“…In patients with juvenile SpA, tarsal affectation is an episode that is frequently accompanied by acute phase inflammation and, sometimes, by chronic phase ankylosis. The combination of inflammatory and structural tarsal alterations is known as ankylosing tarsitis [8]. In our patient, presence of enthesopathy, arthropathy and inflammatory back pain as well as male gender and juvenile-onset of the disease were the findings compatible with the diagnosis of SEA syndrome [2].…”

Section: Discussionsupporting

confidence: 69%

A Rare Coexistence of Seronegative Enthesopathy and Arthropathy Syndrome with Familial Mediterranean Fever

Genç¹

2015

J Rheum Dis Treat

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Section: Discussionsupporting

confidence: 69%

A Rare Coexistence of Seronegative Enthesopathy and Arthropathy Syndrome with Familial Mediterranean Fever

Genç¹

2015

J Rheum Dis Treat

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“…Although peripheral osteoproliferation seems to be the main problem in these patients, very few studies focus on the pathogenesis of tissue inflammation and proliferation (2). We have previously analyzed tendon, enthesis, and joint samples from the midfoot of Mexican patients with ankylosing tarsitis (AT) (64). Our results revealed a scarce leukocyte infiltration accompanied by an osteoid intrusion in the extracellular matrix (ECM), suggesting that, probably, intramembranous ossification of the enthesis and subchondral osteoproliferation could take place.…”

Section: Insights Into the Pathogenesis Of Ankylosing Tarsitismentioning

confidence: 88%

Inflammatory Foot Involvement in Spondyloarthritis: From Tarsitis to Ankylosing Tarsitis

et al. 2021

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Spondyloarthritis (SpA) is a group that includes a wide spectrum of clinically similar diseases manifested by oligoarticular arthritis and axial or peripheral ankylosis. Although axial SpA is predominant in Caucasians and adult-onset patients, juvenile-onset and Latin American patients are characterized by severe peripheral arthritis and particularly foot involvement. The peripheral involvement of SpA can vary from tarsal arthritis to the most severe form named ankylosing tarsitis (AT). Although the cause and etiopathogenesis of axSpA are often studied, the specific characteristics of pSpA are unknown. Several animal models of SpA develop initial tarsitis and foot ankylosis as the main signs, emphasizing the role of foot inflammation in the overall SpA spectrum. In this review, we attempt to highlight the clinical characteristics of foot involvement in SpA and update the knowledge regarding its pathogenesis, focusing on animal models and the role of mechanical forces in inflammation.

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Identificación de sitios ideales para el estudio histopatológico de la tarsitis en pacientes con espondiloartropatías

Cited by 2 publications

References 8 publications

A Rare Coexistence of Seronegative Enthesopathy and Arthropathy Syndrome with Familial Mediterranean Fever

A Rare Coexistence of Seronegative Enthesopathy and Arthropathy Syndrome with Familial Mediterranean Fever

Inflammatory Foot Involvement in Spondyloarthritis: From Tarsitis to Ankylosing Tarsitis

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