Results 61 to 70 of about 1,243,974 (185)

The Churg Strauss Syndrome [PDF]

Journal of the American Society of Nephrology, 1999
During the first half of this century, several authors reported a variant of a small vessel vasculitis that appeared similar to the then recognized polyarteritis nodosa. The condition was distinguished by a significant atopic component, in the form of allergic rhinitis, bronchial asthma ...
JOSEPH A. EUSTACE, TIBOR NADASDY, MICHAEL CHOI   +2 more
openaire   +1 more source

Clinical and Pathological Features of Vasculitic Neuropathy: A Single‐Center Study in China

European Journal of Neurology, Volume 33, Issue 3, March 2026.
Vasculitic neuropathy in mainland China predominantly presents as axonal sensorimotor neuropathy. Systemic VN shows more frequent transmural inflammatory infiltration, whereas EGPA is more common in cases without infiltration. Most treated patients achieved remission, and the overall prognosis was relatively favorable, underscoring the importance of ...
Xiaoyu Zhou, Didi Shan, Bin Wu, Fuchen Liu, Dong Zhang, Pengfei Lin, Wei Li, Yuying Zhao, Chuanzhu Yan, Jingwen Xu   +9 more
wiley   +1 more source

Unusual presentation of temporal bone involvement in Churg–Strauss syndrome

, 2008
Martinez Del Pero M, Moffat D, Sudhoff H. Unusual presentation of temporal bone involvement in Churg–Strauss syndrome. The Journal of Laryngology & Otology.
Martinez Del Pero, M, Sudhoff, Holger ; https://orcid.org/, Moffat, D   +2 more
core   +1 more source

Intracerebral Hemorrhage During the Chronic Phase of Eosinophilic Granulomatosis With Polyangiitis: A Case Report Emphasizing Cerebrovascular Vulnerability

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare form of small‐vessel vasculitis typically associated with eosinophilia, asthma, and systemic inflammation. Although peripheral neuropathies are relatively common, central nervous system involvement, especially intracerebral hemorrhage during the remission phase of EGPA, is uncommon,
Shinya Watanabe, Masatoshi Kasuya, Yasushi Shibata   +2 more
wiley   +1 more source

Myocarditis in the Modern Era: Navigating Diagnosis, Innovative Treatments, the COVID‐19 Challenge and the Role of Artificial Intelligence

Cardiology Research and Practice, Volume 2026, Issue 1, 2026.
Myocarditis is an inflammatory disease of the myocardium with diverse aetiologies, ranging from infections and autoimmune processes to drug‐induced reactions. Clinical manifestations vary widely from mild chest discomfort to life‐threatening complications such as acute heart failure, cardiogenic shock and sudden cardiac death. Although the diagnosis of
Kevin Mohee, Ibrahim Antoun, Robert Ambrogetti, Mahmoud Eldesouky, Riyaz Somani, André Ng, Sanjay S. Bhandari, Irfan Ahmad   +7 more
wiley   +1 more source

Churg-Strauss syndrome with montelukast [PDF]

Thorax, 2001
The case report by Tuggey and Hosker1 is similar to many of the cases of Churg-Strauss syndrome (CSS) which we have reported in association with zafirlukast,2 montelukast, and fluticasone/salmeterol.3 It also shares many similarities with the reports of CSS with inhaled steroid monotherapy.4 5 While a temporal relationship with the use of leukotriene
openaire   +2 more sources

Churg-Strauss syndrome and hemorragic vasculitis [PDF]

Dermatology Reports, 2011
Churg-Strauss syndrome (CSS) is a rare syndrome characterized by sinusitis, asthma and peripheral eosinophilia. This vasculitic syndrome affects medium and small-sized vessels, the lung being the most commonly affected organ, followed by the skin. The authors report a case of a 59-year-old male with a past history of asthma and allergic rhinitis.
Rui Moreira Marques, Ana Rita Cabral, Antonio Monteiro, Pedro Henriques   +3 more
openaire   +3 more sources

Delayed Diagnosis of Pulmonary‐Renal Syndrome Presenting as Chronic Hemoptysis Leading to ESRD

Case Reports in Pediatrics, Volume 2026, Issue 1, 2026.
This case demonstrates the importance of recognizing the various presentations of MPA in pediatric patients and highlights the need for more documentation and discussion of MPA in the current literature in order to increase awareness of MPA and provide possible basis for future diagnostic criteria.
Kalie Nuss, Katiana Garagozlo, Lilliana Barillas-Arias, Satabdi Datta Choudhury   +3 more
wiley   +1 more source

Spontaneous Hemothorax and Hemoptysis in Granulomatosis With Polyangiitis: A Case Report

Clinical Case Reports, Volume 13, Issue 9, September 2025.
Histologic lung section illustrating chronic vasculitis characteristic of GPA. ABSTRACT Spontaneous hemothorax is a rare but potentially life‐threatening manifestation of granulomatosis with polyangiitis (GPA). This case highlights the importance of considering vasculitis in unexplained hemothorax and underscores the role of early surgical intervention
Paolo Scanagatta, Sara Cagnetti, Casimiro Eugenio Giorgetta, Francesco Inzirillo, Eugenio Ravalli, Giuseppe Naldi, Manuela Agozzino, Gianluca Ancona   +7 more
wiley   +1 more source

A Presentation of Massive Hemoptysis in a Patient with Churg-Strauss Syndrome

Canadian Respiratory Journal, 2014
Given that Churg-Strauss syndrome is a systemic small-vessel vasculitis, it is not usually considered in patients who present with massive hemoptysis, which is typically caused by bronchiectasis, cancer or, in some cases, aberrant bronchial arteries ...
Fadi Hikmat, David B Pearse, Mahendra Damarla   +2 more
doaj   +1 more source