Results 41 to 50 of about 8,749 (184)

Wells syndrome: clinical findings and management in a large cohort of 48 patients

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Background and Objectives: Wells syndrome (WS) is a rare inflammatory skin disorder typically characterized by erythematous, edematous, and pruritic plaques. Despite its distinct histopathological features, WS remains an underdiagnosed disease due to its variable clinical presentations and overlap with other dermatological conditions.
Marco Adriano Chessa, Silvia Robuffo, Tullio Brunetti, Luca Rapparini, Bianca Maria Piraccini, Cosimo Misciali, Beatrice Raone, Iria Neri, Federica Filippi   +8 more
wiley   +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

Asma e síndrome de Churg-Strauss Asthma and Churg-Strauss syndrome

Jornal Brasileiro de Pneumologia, 2006
Relata-se o caso de uma mulher de 25 anos com síndrome de Churg-Strauss, cujos sintomas surgiram aos dezesseis anos, logo após o início do uso de contraceptivo oral.
Soloni Afra Pires Levy, Alfeu Tavares França, Denise de La Reza, Solange Oliveira Rodrigues Valle, Ana Helena Pereira Correia   +4 more
doaj   +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

Churg-Strauss syndrome: A case report [PDF]

Vojnosanitetski Pregled, 2013
Introduction. Churg-Strauss syndrome (CSS) is an allergic granulomatous angiitis, a rare disease of small and medium arteries and veins, associated with the presence of perinuclear antineutrophil cytoplasmic antibodies (p-ANCA).
Dinić Miroslav Ž., Kandolf-Sekulović Lidija, Zolotarevski Lidija, Zečević Radoš D.   +3 more
doaj   +1 more source

Eosinofiilsed kopsuhaigused [PDF]

, 2012
Eosinofiilsete kopsuhaiguste (EK) puhul on peamiseks koekahjustust põhjustavaks rakuliigiks eosinofiilid, mis kogunevad kopsude interstiitsiumi ja hingamisteedesse.
Altraja, Alan, Makke, Vahur, Püttsepp, Enn   +2 more
core   +2 more sources

The Dental Status of Patients Taking Common Biologic Agents: A Single‐Center Cross‐Sectional Study

Oral Diseases, Volume 31, Issue 8, Page 2641-2651, August 2025.
ABSTRACT Objectives Despite expanding use and medical applications, little is known about the impact of biologic agents (BAs) on dental treatment. The aim of this study was to investigate the dental status of patients on common classes of BAs to understand treatment needs and use in this population.
Shivani Shah, Nila Veerabagu, Nana A. A. Essel, Neda Mahjour, Katherine France   +4 more
wiley   +1 more source

Severe eosinophilic syndrome associated with the use of probiotic supplements: a new entity? [PDF]

, 2012
Severe eosinophilic syndromes related to the administration or use of unsuspected immunogenic substances have been described previously. Many of these diseases presented initially as clusters or isolated cases.
Article Id, Fabian A. Mendoza, Lawrence Kenyon, Sergio A. Jimenez, Shivani Purohit   +4 more
core   +2 more sources

Central retinal artery occlusion in a patient with ANCA-negative Churg-Strauss syndrome

Clinical Ophthalmology, 2012
Yuji Kumano,1 Noriko Yoshida,2 Satoru Fukuyama,3 Masanori Miyazaki,2 Hiroshi Enaida,2 Takaaki Matsui11Ohshima Hospital of Ophthalmology, Fukuoka, 2Department of Ophthalmology, 3Research Institute for Diseases of the Chest, Graduate School of Medical ...
Miyazaki M, Enaida H, Matsui T, Kumano Y, Yoshida N, Fukuyama S   +5 more
doaj  

Poliangeitis amb Granulomatosis eosinofílica i asma al·lèrgica; dues monedes amb una mateixa cara? [PDF]

, 2013
La síndrome de Churg-Strauss o Poliangeitis amb Granulomatosis eosinofílica (EGPA), clàssicament s'ha vinculat a un substrat asmàtic d'origen al·lèrgic. No obstant, l'evidència en aquest sentit és equívoca.
Bosch Gil, Josep Àngel, Ramentol Sintas, Marc, Solans Laqué, Roser, Universitat Autònoma de Barcelona. Departament de Medicina, Universitat Autònoma de Barcelona. Facultat de Medicina   +4 more
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