Results 41 to 50 of about 1,243,974 (185)

Chronic Rhinosinusitis and Nasal Polyps in Eosinophilic Granulomatosis With Polyangiitis: A Scoping Review

International Forum of Allergy &Rhinology, Volume 16, Issue 9, Page 996-1011, September 2026.
ABSTRACT Background Chronic rhinosinusitis (CRS) is one of the most common manifestations of eosinophilic granulomatosis with polyangiitis (EGPA), often preceding the diagnosis of systemic vasculitis by several years. The sinonasal presentation of EGPA typically resembles CRS with nasal polyps (CRSwNP), making it clinically indistinguishable from those
Alisha Sharma, Alyssa Y. Li, Teruko Kishibe, Dennis Wong, Kevin M. Sanders, Maggie Jiang, Heedo Lee, Christine Song, Kieran Mcintyre, Christian Pagnoux, Yvonne Chan, John M. Lee, Daniel J. Lee   +12 more
wiley   +1 more source

“Peripheral Neuropathy Crippling Bronchial Asthma”: Two Rare Case Reports of Churg-Strauss Syndrome

Case Reports in Pulmonology, 2014
Churg-Strauss syndrome (CSS) is a rare cause of vasculitic neuropathy. Although rare and potentially fatal, Churg-Strauss syndrome (CSS) is easily diagnosable and treatable.
Kamal Kishore Pandita, Khalid Javid Bhat, Sushil Razdan, R. P. Kudyar   +3 more
doaj   +1 more source

Churg–Strauss syndrome presenting with eosinophilic myocarditis: A diagnostic challenge

Revista Portuguesa de Cardiologia, 2013
Churg–Strauss syndrome (CSS) is an unusual disease that presents as systemic vasculitis and peripheral eosinophilia in patients with an atopic constitution.
Ana Sofia Correia, Alexandra Gonçalves, Vítor Araújo, João Almeida e Silva, José Manuel Pereira, Pedro Rodrigues Pereira, Manuel Pizarro, João Carlos Silva, Maria Júlia Maciel   +8 more
doaj   +1 more source

Cardiac involvement in Churg‐Strauss syndrome [PDF]

Arthritis & Rheumatism, 2010
AbstractObjectiveChurg‐Strauss syndrome (CSS) is a rare form of systemic vasculitis. Previous studies showing cardiac involvement in CSS patients were limited in the number of patients and were often based solely on clinical manifestations. The aim of the present study was to determine in detail the incidence of cardiac involvement in a large ...
Dennert, Robert M., van Paassen, Pieter, Schalla, Simon, Kuznetsova, Tatiana, Alzand, Becker S., Staessen, Jan A., Velthuis, Sebastiaan, Crijns, Harry J., Tervaert, Jan Willem Cohen, Heymans, Stephane   +9 more
openaire   +2 more sources

Synovial fluid proteomic biomarkers in periprosthetic joint infection: A systematic review with gene ontology and protein network analyses

Journal of Experimental Orthopaedics, Volume 13, Issue 3, July 2026.
Abstract Purpose Periprosthetic joint infection (PJI) is a severe complication of total joint arthroplasty associated with significant morbidity, implant failure and increased healthcare costs. Diagnosis remains challenging, particularly in low‐grade and culture‐negative infections, because conventional markers lack specificity.
Giorgia Lucia Benedetto, Elvira Immacolata Parrotta, Raffaele Covello, Giovanni Cuda, Giorgio Gasparini, Olimpio Galasso, Umile Giuseppe Longo, Michele Mercurio   +7 more
wiley   +1 more source

Churg-Strauss syndrome - High resolution CT and pathologic findings

, 2005
Objectives: the purpose of this study was to evaluate high-resolution CT findings in 7 patients with Churg-Strauss syndrome and to compare the CT with the histopathologic findings.Materials and Methods: High-resolution CT scans of 7 asthmatic patients (4
Churg, A., Ajzen, S. A., Silva, CIS, Fujimoto, K., Johkoh, T., Muller, N. L.   +5 more
core   +1 more source

Oral Angiolymphoid Hyperplasia With Eosinophilia Exhibiting Cutaneous‐Type Histopathologic Features: Clinical Regression Following Hormonal Withdrawal and a 50‐Year Review

Journal of Cutaneous Pathology, Volume 53, Issue 6, Page 491-501, June 2026.
Case report of a 30‐year‐old female. Asymptomatic, red‐purple hyperplastic lesion extending from teeth 21 to 25, with bleeding upon manipulation. Differential diagnosis included: inflammatory gingival hyperplasia, plasma cell gingivitis, leukemia, and Wegener's granulomatosis.
Pedro Vinícius Santos de Jesus, Louise Cristina Santos, Gilberth Tadeu Dos Santos Aciole, John Lennon Silva Cunha, Nicole Lonni, Matheus Antoni da Silva Costa, Elena Riet Correa Rivero, Rogério Gondak, Ricardo Luíz Cavalcanti de Albuquerque‐Júnior   +8 more
wiley   +1 more source

From Nerves to Vessels: Unmasking Churg‐Strauss Behind Polyneuropathy

Clinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT Eosinophilic granulomatosis with polyangiitis (EGPA), formerly Churg‐Strauss vasculitis, is a rare systemic autoimmune disease. Neurological involvement is a significant complication. This report details a case of EGPA with severe, progressive polyneuropathy and atypical serological findings, highlighting diagnostic challenges and the ...
Hiba Antar, Sylvana Balhas, Zeinab El Mawla   +2 more
wiley   +1 more source

Small bowel involvement documented by capsule endoscopy in Churg-Strauss syndrome [PDF]

, 2016
Churg-Strauss syndrome is a small and medium vessel vasculitis and is also known as allergic granulomatous angiitis. Gastrointestinal involvement is common in patients with Churg-Strauss syndrome (20-50%).
Kieffer, Pierre, Martzolf, Lionel, Beye, Birane, Sondag, Daniel, Claude, Pierre, Lesur, Gilles   +5 more
core   +1 more source

Síndroma de Churg-Strauss – a propósito de um caso clínico

Revista Portuguesa de Pneumologia, 2005
Resumo: A síndroma de Churg-Strauss (SCS) é uma vasculite sistémica pouco comum, que atinge preferencialmente vasos de pequeno calibre, envolve múltiplos órgãos e surge quase sempre associada a asma e eosinofilia.Os autores fazem uma revisão sobre
Susana Oliveira, Catarina Mendonça, José Eduardo Ambar, Berta Mendes   +3 more
doaj   +1 more source