Results 71 to 80 of about 6,719 (245)
Leprosy with Atypical Skin Lesions Masquerading as Relapsing Polychondritis
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 +5 more
doaj +1 more source
Objective Although previous studies show that primary prophylaxis against Pneumocystis jirovecii pneumonia (PJP) is effective in patients with rheumatic diseases receiving immunosuppressive treatment, there is limited evidence regarding the optimal timing for prophylaxis withdrawal.
Ju Yeon Kim +5 more
wiley +1 more source
Hematopoietic stem cell transplantation in autoimmune disorders: from immune-regulatory processes to clinical implications [PDF]
K
Nakken, Britt +3 more
core +1 more source
Relapsing Polychondritis that Recovers Rapidly with One-Dose Steroid: A Case Report
Relapsing polychondritis is a rare, autoimmune, multisystemic disease that presents with episodic inflammatory process of the cartilages. We report a case of a 48-year-old woman who presented to our otolaryngology clinic with complaints of pain, eritema,
Abdurrahman Bozkurttan +4 more
doaj +1 more source
Keywords: Ear Diseases; Ear, External; Polychondritis, Relapsing.
Cristina Ponte, Carla Macieira
doaj +1 more source
ABSTRACT Background and Aims Cutaneous leishmaniasis (CL) represents the most common form of leishmaniasis. It imposes a significant medical burden due to long‐lasting ulcers and disfiguring scars, underscoring the need for comprehensive CL control strategies, particularly in endemic regions.
Bahareh Abtahi‐Naeini +5 more
wiley +1 more source
A Unique Case of Relapsing Polychondritis Presenting with Acute Pericarditis
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 +2 more
doaj +1 more source
ABSTRACT VEXAS syndrome is caused by somatic mutations in the UBA1 gene and includes features of both autoinflammatory and myeloid diseases. Among several treatment options, JAK inhibitors have proven effective, especially ruxolitinib. However, anemia is often present in VEXAS syndrome.
Dominik Kiem +7 more
wiley +1 more source

