Results 71 to 80 of about 3,083 (191)

Atypical Manifestations of Old World Cutaneous Leishmaniasis: A Systematic Review and Clinical Atlas of Unusual Clinical and Specific Anatomical Presentations

open access: yesHealth Science Reports, Volume 8, Issue 9, September 2025.
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

VEXAS Syndrome and Substance Use Disorders: A Large‐Scale, Propensity‐Matched, Case‐Control Analysis Revealing Immune‐Mediated Comorbidities

open access: yes
International Journal of Dermatology, Volume 65, Issue 3, Page 584-586, March 2026.
Kritin K. Verma   +4 more
wiley   +1 more source

Momelotinib Is Effective in Treatment for VEXAS Syndrome: Two Cases Within the AGMT Austrian Myeloid Registry

open access: yesEuropean Journal of Haematology, Volume 115, Issue 3, Page 299-302, September 2025.
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

Saddle Nose in Granulomatosis With Polyangiitis (GPA) vs. Non‐GPA Patients With Septal Perforations

open access: yesLaryngoscope Investigative Otolaryngology, Volume 10, Issue 4, August 2025.
This is a retrospective case‐control study comparing patients with nasal septal perforations with GPA vs. non‐GPA etiologies. GPA patients had larger perforations and 19 times higher odds of being associated with saddle nose deformity independent of perforation size.
Nitish Kumar   +6 more
wiley   +1 more source

Relapsing polychondritis with different types of ocular inflammations

open access: yes, 2015
Nana Furuya, Toshiyuki Oshitari, Jiro Yotsukura, Takayuki Baba, Shuichi Yamamoto Department of Ophthalmology and Visual Science, Chiba University, Graduate School of Medicine, Chuo-ku, Chiba, Japan Abstract: We were presented with two cases of relapsing
Oshitari T   +4 more
core  

Clinical characteristics of patients with relapsing polychondritis.

open access: yes, 2018
Clinical characteristics of patients with relapsing polychondritis.
Kenji Takai (2623126)   +10 more
core   +1 more source

Síndrome de Erasmus Associada à Policondrite Recidivante: Relato de Caso / Erasmus’ Syndrome in Association with Relapsing Polychondritis: a Case Report

open access: yesRevista Ciências em Saúde, 2013
Introdução: A silicoesclerodermia foi descrita pela primeira vez por Erasmus, e é consequência de uma resposta inflamatória desencadeada pela sílica, envolvendo a liberação de mediadores que causam alteração na imunidade celular e humoral, levando a ...
Jacqueline Foelkel Pignatari   +3 more
doaj   +1 more source

Expert Perspective: Hematologic Malignancies and Vasculitis

open access: yes
Arthritis &Rheumatology, Volume 77, Issue 10, Page 1305-1316, October 2025.
Michelle L. Robinette, Hetty E. Carraway
wiley   +1 more source

Unusual cause of the left main bronchus stenosis: relapsing polychondritis [PDF]

open access: yes
Relapsing polychondritis is a rare disease that causes inflammation and destruction of cartilage and connective tissue. It can be associated with other autoimmune rheumatologic and hematologic diseases.
Aydin, Yener   +2 more
core   +1 more source

Posterior Scleritis and Myelodisplasia in Relapsing Polychondritis- Case Report and Literature Review

open access: yesVision Pan-America, 2016
Relapsing Polychondritis (RP) is a rare, recurrent and autoimmune multisytem disorder affecting cartilaginous structures, such as: auricles, joints, nasal septum, larynx and tracheobronchial tree.
nadine sousa marques   +7 more
doaj   +1 more source

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