Results 21 to 30 of about 391,559 (209)
Рецидивирующий полихондрит, развившийся после пирсинга (клинический случай) [PDF]
, 2023 Relapsing polychondritis (RPC) belongs to a group of rare rheumatic diseases with poorly understood etiology and pathogenesis. It is based on progressive systemic inflammatory damage to the cartilage tissue, primarily affecting ears, nose, trachea and ...
A. A. Godzenko +7 more
core +2 more sources
Frontiers in Immunology, 2022 Vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome is an autoinflammatory disease caused by somatic variants in the UBA1 gene that lead to severe systemic inflammation and myelodysplastic syndrome.
Y. Kunishita +7 more
semanticscholar +1 more source
Hemorrhagic Stroke in Relapsing Polychondritis: A Rare Complication of a Rare Disease
Case Reports in Rheumatology, 2020 Background. Relapsing Polychondritis is a rare rheumatologic condition with multisystem involvement. Common presenting symptoms are auricular and nasal chondritis. Common complications include hearing loss and cardiac involvement.
Benjamin Chaucer +3 more
doaj +1 more source
Dapsone-induced methaemoglobinaemia in relapsing polychondritis
BMJ Case Reports, 2022 © BMJ Publishing Group Limited 2022. No commercial reuse. See rights and permissions. Published by BMJ. DESCRIPTION Dapsone (4,4'-diaminodiphenyl sulfone) is an antibacterial and antiinflammatory drug, sometimes used for rheumatic disease. It is known to
Tomohiro Yoshida +3 more
semanticscholar +1 more source
Early Recognition and Treatment of Relapsing Polychondritis
Cureus, 2022 We describe the case of a 60-year-old Japanese man with relapsing polychondritis (RP). The patient was referred to Hamanomachi Hospital due to mild elevation of C-reactive protein and mild anemia on medical checkup without any symptoms.
T. Yanagihara +9 more
semanticscholar +1 more source
Anti-phospholipid-antibodies in patients with relapsing polychondritis [PDF]
, 1998 Relapsing polychondritis (RP) is an extremly rare multisystemic disease thought to be of autoimmune origin. In order to assess if RP is associated with anti-phospholipid antibodies (aPL), clinical data and sera of 21 patients with RP were collected in a ...
B Lang +11 more
core +1 more source
Subglottic Mass as Isolated Manifestation of Relapsing Polychondritis at Presentation [PDF]
, 2021 Relapsing polychondritis (RP) is a rare systemic disease that is characterized by recurrent episodic inflammation of the cartilaginous structures of the body, resulting in their progressive destruction and subsequent replacement with fibrotic scar.
Gaetano Motta +4 more
core +2 more sources
Relapsing Polychondritis and Aseptic Meningoencephalitis
Internal medicine, 2022 We herein report a 49-year-old Japanese man with relapsing polychondritis (RP) and aseptic meningoencephalitis. Four years ago, the patient was diagnosed with RP. Prednisolone (PSL) was started at 30 mg/day, and the symptoms promptly disappeared. However,
K. Yokota +4 more
semanticscholar +1 more source
Audio-vestibular symptoms in systemic autoimmune diseases [PDF]
, 2018 Immune-mediated inner ear disease can be primary, when the autoimmune response is against the inner ear, or secondary. The latter is characterized by the involvement of the ear in the presence of systemic autoimmune conditions. Sensorineural hearing loss
Adelchi, Croce +7 more
core +1 more source
Relapsing polychondritis causing breathlessness: Two case reports
World Journal of Clinical Cases, 2022 BACKGROUND Relapsing polychondritis is a rare multisystem autoimmune disease that mainly involves systemic cartilage and proteoglycan-rich tissues. If the larynx and trachea are involved, the patient’s condition deteriorates rapidly.
Songyu Zhai +4 more
semanticscholar +1 more source