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Relapsing Polychondritis [PDF]

open access: yesCase Reports in Dermatological Medicine, 2014
Relapsing polychondritis (RP) is a rare systemic disease characterized by recurrent, widespread chondritis of the auricular, nasal, and tracheal cartilages. Additional clinical features include audiovestibular dysfunction, ocular inflammation, vasculitis,
Beata Sosada   +2 more
doaj   +5 more sources

Bronchoscopy-Guided Intervention Therapy With Extracorporeal Membrane Oxygenation Support for Relapsing Polychondritis With Severe Tracheobronchomalacia: A Case Report and Literature Review

open access: yesFrontiers in Medicine, 2021
Relapsing polychondritis is an immune disorder of unknown etiology involving multiple systems that is characterized by persistent inflammation and destruction of cartilage, including the ears, nose, costal, joint, and airways.
Pengcheng Zhou   +7 more
doaj   +2 more sources

Respiratory-predominant relapsing polychondritis: the role of PET scan in making this challenging diagnosis [PDF]

open access: yesEuropean Journal of Case Reports in Internal Medicine
Relapsing polychondritis is a rare, immune-mediated, multisystemic disease characterized by recurrent inflammation of cartilaginous and proteoglycan-rich tissues. Its diagnosis may be challenging due to its rarity and wide clinical variability. It can be
Daniela Alves   +5 more
doaj   +2 more sources

Respiratory subtype of relapsing polychondritis frequently presents as difficult asthma: a descriptive study of respiratory involvement in relapsing polychondritis with 13 patients from a single UK centre

open access: yesERJ Open Research, 2021
Introduction Relapsing polychondritis is a rare multisystem vasculitis characterised by recurrent cartilage inflammation. Respiratory involvement, of which tracheobronchomalacia (TBM) is the commonest form, is difficult to treat and is linked to ...
Shirish Dubey   +9 more
doaj   +2 more sources

Relapsing polychondritis

open access: yesSão Paulo Medical Journal
PURPOSE: This article describes a clinically-diagnosed case of relapsing polychondritis (RP), attended at the Hospital São Paulo, and presents a literature review of the subject.
Lincoln Sakiara Miyasaka   +3 more
doaj   +3 more sources

Recurrent lymphocytic meningitis and progressive dementia: manifestations of relapsing polychondritis: a case report [PDF]

open access: yesBMC Neurology
Background Recurrent polychondritis is an immune-mediated systemic disease that affects cartilaginous and non-cartilaginous structures. Despite being rare, multiple neurological manifestations have been described, such as involvement of cranial nerves ...
Vanessa Ocampo-Piraquive   +3 more
doaj   +2 more sources

Relapsing polychondritis: commentary

open access: yesReumatismo, 2002
Relapsing Polychondritis (RP) is a multisystem disease of unknown etiology characterized by episodic inflammation of cartilage and potentially progressive degeneration of cartilaginous tissue, such as auricular, nasal and laryngotracheobronchial ...
I. Herrera, A. Mannoni, R.D. Altman
doaj   +4 more sources

Relapsing polychondritis

open access: yesSaudi Journal of Medicine and Medical Sciences, 2016
Arulprakash Sarangapani   +2 more
doaj   +3 more sources

Relapsing Polychondritis [PDF]

open access: yesRespiration, 1998
In this article, we report on a 40-year-old man with relapsing polychondritis (RP) of the tracheobronchial tree without clinical manifestations of other systems including nasal septum and earlobe cartilage involvement. The illness was diagnosed histologically, and treatment with procaine penicillin was successful.
Yalcinkaya, I   +3 more
  +9 more sources

Evaluation of airway involvement and treatment in patients with relapsing polychondritis

open access: yesScientific Reports, 2023
Airway involvement in relapsing polychondritis (RP) can be debilitating and life threatening, often requiring interventional procedures. If standard therapies including systemic corticosteroid and immunosuppressive agents are ineffective, airway stenting
H. Handa   +4 more
semanticscholar   +1 more source

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