Inflammatory arthritis and crystal arthropathy: Current concepts of skin and systemic manifestations

Fazel, Mahdieh; Merola, Joseph F.; Kurtzman, Drew J.B.

doi:10.1016/j.clindermatol.2018.04.010

Cited by 6 publications

(9 citation statements)

References 128 publications

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“…Still's disease was initially reported as a childhood disease. Still's disease, systemic juvenile idiopathic arthritis (sJIA), and AOSD exist on a spectrum, and it has been generally considered that some cases occurring before age 16 years are sJIA while cases presenting after age 18 years are AOSD [91]. However, there are indeterminate cases in which sJIA is identical to adolescent-onset Still's disease.…”

Section: Psoriasis and Adult-onset Still's Diseasementioning

confidence: 99%

Psoriasis and Connective Tissue Diseases

Yamamoto

2020

IJMS

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Psoriasis is a chronic systemic inflammatory disease with various co-morbidities, having been recently considered as a comprehensive disease named psoriatic disease or psoriatic syndrome. Autoimmune diseases are one form of its co-morbidities. In addition to the genetic background, shared pathogenesis including innate immunity, neutrophil extracellular trap (NETs), and type I interferon, as well as acquitted immunity such as T helper-17 (Th17) related cytokines are speculated to play a significant role in both psoriasis and connective tissue diseases. On the other hand, there are definite differences between psoriasis and connective tissue diseases, such as their pathomechanisms and response to drugs. Therefore, we cannot expect that one stone kills two birds, and thus caution is necessary when considering whether the administered drug for one disease is effective or not for another disease. In this review, several connective tissue diseases and related diseases are discussed from the viewpoint of their coexistence with psoriasis.

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Section: Psoriasis and Adult-onset Still's Diseasementioning

confidence: 99%

Psoriasis and Connective Tissue Diseases

Yamamoto

2020

IJMS

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“…17,18 In RA, they frequently occur in the pretibial region and at the malleoli, 26 making them difficult to distinguish from venous ulceration. They usually appear rapidly, are slow to heal, 18,27 and occur in patients with longstanding seropositive disease and joint destruction. 17,28 Cutaneous vasculitis in RA is often associated with petechiae, purpura, and Bywater lesions.…”

Section: Discussionmentioning

confidence: 99%

Diagnosis and Management of a Chronic Lower-Limb Wound in a Patient with Felty Syndrome

Burgess

Cummins²,

Wong³

et al. 2022

Adv Skin Wound Care

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“…Still's disease was initially reported as a childhood disease. Adult-onset Still's disease (AOSD) and systemic juvenile idiopathic arthritis (sJIA) exist on a spectrum, and it has been generally considered that some cases occurring before age 16 years are sJIA while cases presenting after age 18 years are AOSD [1]. However, there are indeterminate cases in which sJIA is identical to adolescent-onset Still's disease.…”

Section: Sirmentioning

confidence: 99%