Results 41 to 50 of about 272 (99)

Leprosy with Atypical Skin Lesions Masquerading as Relapsing Polychondritis

Case Reports in Infectious Diseases, 2016
Leprosy can present with a variety of clinical manifestations depending on the immune status of the individual. After dermatological and neurological involvement, rheumatic features specially various forms of arthritis are the third most common ...
Punit Pruthi, Hariharan Munganda, Amit Bangia, Uma Rani, Rajesh Budhiraja, Swapnil Brajpuriya   +5 more
doaj   +1 more source

Unmasking the Hidden Threat: The Role of Left Ventricular Subendocardial Involvement in Autoimmune Rheumatic Disease

Clinical Cardiology, Volume 48, Issue 1, January 2025.
Cardiac magnetic resonance‐detected left ventricular subendocardial late gadolinium enhancement was more strongly associated with adverse outcomes in autoimmune rheumatic disease patients. LV, left ventricular. LGE, late gadolinium enhancement. ABSTRACT Background Late gadolinium enhancement (LGE) has been found in patients with autoimmune rheumatic ...
Danni Wu, Xiao Li, Tianchen Guo, Xiaojin Feng, Xinhao Li, Yining Wang, Wei Chen   +6 more
wiley   +1 more source

Síndrome de Sweet e policondrite recidivante reveladores de síndrome mielodisplásica Sweet's Syndrome and relapsing polychondritis signal myelodysplastic syndrome

Anais Brasileiros de Dermatologia, 2011
Certas dermatoses, pertencentes ao grupo das síndromes paraneoplásicas mucocutâneas, podem ser o prenúncio de uma neoplasia previamente não conhecida. Tanto a síndrome de Sweet como a policondrite recidivante incluem-se neste grupo. A síndrome de Sweet e
Filipa da Encarnação Roque Diamantino, Pedro Manuel Oliveira da Cunha Raimundo, Ana Isabel Pina Clemente Fidalgo   +2 more
doaj   +1 more source

Relapsing Polychondritis Associated With Thyroid Carcinoma: A First Malagasy Case

Case Reports in Otolaryngology, Volume 2025, Issue 1, 2025.
Relapsing polychondritis (RP) is a rare disease characterized by recurrent systemic inflammation affecting cartilaginous tissues and proteoglycan‐rich tissues. The disease may present in several clinical variants, which can delay diagnosis. Corticosteroids are the treatment of choice for RP. In rare cases, RP can be paraneoplastic.
Oliva Henintsoa Rakotonirainy, Mamonjisoa Olivier Andrianiaina, Lalao Nomenjanahary Rakotonirina, Volatantely Ratovonjanahary, Fahafahantsoa Rabenja Rapelanoro, M. Tayyar Kalcioglu   +5 more
wiley   +1 more source

VEXAS syndrome initially presenting as relapsing polychondritis and progressing into neutrophilic dermatosis with systemic symptoms over a 5‐year period

International Journal of Dermatology, EarlyView.
Kaori Kashino, Naomi Tsuchida, Ayaka Maeda, Yuri Uchiyama, Yohei Kirino, Naomichi Matsumoto, Toshihisa Hamada   +6 more
wiley   +1 more source

Pediatric Red Ear Syndrome Misdiagnosed as Relapsing Polychondritis: A Case Report and Review of Literature

Case Reports in Pediatrics, Volume 2025, Issue 1, 2025.
Red ear syndrome (RES) is a rare clinical entity presenting with paroxysmal erythema of one or both ears associated with a burning sensation or earache. The onset of symptoms could be either spontaneous or triggered by touch, stress, coughing, sneezing, neck movements, chewing, and combing hair.
Nicolas Sandakly, Georgio El Koubayati, Jeannette Sarkis, Fady Haddad, Maria Moschovi   +4 more
wiley   +1 more source

A Unique Case of Relapsing Polychondritis Presenting with Acute Pericarditis

Case Reports in Rheumatology, 2013
Relapsing polychondritis (RP) is an inflammatory disease of the cartilaginous tissue primarily affecting the cartilaginous structures of the ear, nose, joints, and the respiratory system.
John V. Higgins, Uma Thanarajasingam, Thomas G. Osborn   +2 more
doaj   +1 more source

Optical genome mapping with genome sequencing identifies subtelomeric Xq28 deletion and inserted 7p22.3 duplication in a male with multisystem developmental disorder

American Journal of Medical Genetics Part A, Volume 194, Issue 12, December 2024.
Abstract We report a 17‐year‐old male with supravalvular stenosis, initial failure to thrive and delayed early development, short stature, acromelia, dysmorphic facial features, hypertelorism, macrocephaly, syringomyelia, hypertension, and anxiety disorder.
Jorge L. Rodriguez‐Gil, Peter L. Nagy, Uta Francke   +2 more
wiley   +1 more source

Relapsing polychondritis

São 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, Ary de Andrade Junior, Carlos Eduardo Bueno, Alvaro Nagib Atallah   +3 more
doaj   +1 more source

Relapsing Polychondritis: An Updated Review

Biomedicines, 2018
Relapsing polychondritis is an immune-mediated systemic disease characterized by recurrent episodes of inflammation of cartilaginous and proteoglycan-rich tissues, resulting in progressive anatomical deformation and functional impairment of the involved ...
Francesco Borgia, Roberta Giuffrida, Fabrizio Guarneri, Serafinella P. Cannavò   +3 more
doaj   +1 more source