Results 81 to 90 of about 8,486 (210)

High detection rate for perivascular deposits of immunoglobulins in immune complex vasculitis from biopsies of early macular lesions

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 4, Page 479-485, April 2025.
Summary Background In immune complex vasculitis the detection of perivascular immunoglobulins by direct immunofluorescence (DIF) not only helps to confirm the diagnosis, but also to define the type of vasculitis (e.g., IgA‐, IgG/IgM‐, rheumatoid or cryoglobulinemic vasculitis).
Luisa Herda, Christiane Michl, Cord Sunderkötter   +2 more
wiley   +1 more source

Manifestações otorrinolaringológicas nas doenças reumáticas auto-imunes Otorhinolaryngologic manifestations of autoimmune rheumatic diseases

Revista Brasileira de Reumatologia, 2006
As manifestações otorrinolaringológicas nas doenças reumáticas representam um desafio diagnóstico para o reumatologista, o otorrinolaringologista e o médico generalista.
Daniela Bergamim Pereira, Juliana Lasmar Ayres do Amaral, José Carlos Mansur Szajubok, Sônia Maria Anti Loduca Lima, Wiliam Habib Chahade   +4 more
doaj   +1 more source

Avoiding early diagnosis

Journal of General and Family Medicine, Volume 26, Issue 4, Page 292-296, July 2025.
Takao Wakabayashi, Goh Keng Wee, Mikinosuke Ishibashi, Yoshiki Akiyama, Naoki Kanda, Tomoyuki Watanabe   +5 more
wiley   +1 more source

Hohe Nachweisrate perivaskulärer Ablagerungen von Immunglobulinen bei Immunkomplex‐Vaskulitis aus Biopsien von frühen makulären Effloreszenzen

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 4, Page 479-486, April 2025.
Zusammenfassung Hintergrund Bei Immunkomplexvaskulitiden ist der Nachweis perivaskulärer Immunglobuline mittels direkter Immunfluoreszenz (DIF) nicht nur hilfreich zur Diagnosebestätigung, sondern auch zur Bestimmung der Vaskulitisform (IgA‐ IgG/IgM‐, rheumatoide oder kryoglobulinämische Vaskulitis).
Luisa Herda, Christiane Michl, Cord Sunderkötter   +2 more
wiley   +1 more source

Ten‐year follow‐up of a case of eosinophilic granulomatous with polyangiitis

ESC Heart Failure, Volume 12, Issue 3, Page 2361-2366, June 2025.
Jiange Qiao, Mingjie Cao, Tao Ren, Chen Gong, Zhijun Jie, Qingmin Yang, Jindong Shi   +6 more
wiley   +1 more source

Churg-Strauss syndrome following cessation of allergic desensitization vaccination: a case report

Journal of Medical Case Reports, 2010
Introduction Churg-Strauss syndrome is a vasculitis of medium to small sized vessels. Diagnosis is mainly clinical with findings of asthma, eosinophilia, rhinosinusitis and signs of vasculitis in major organs.
Mokri Bahareh, Talischi Firouzeh, Fayazi Nader, Cheraghvandi Ali, Tafti Saeid, Masjedi Mohammad   +5 more
doaj   +1 more source

Allergic bronchopulmonary aspergillosis: diagnostic and treatment challenges [PDF]

, 2016
Allergic bronchopulmonary aspergillosis (ABPA) is a pulmonary disorder, occurring mostly in asthmatic and cystic fibrosis patients, caused by an abnormal T-helper 2 lymphocyte response of the host to Aspergillus fumigatus antigens.
CINICOLA, BIANCA LAURA, DUSE, MARZIA, Laitano, Rossella, LEONARDI, LUCIA   +3 more
core   +1 more source

Wound, pressure ulcer, and burn guidelines (2023)―4: Guidelines for the management of connective tissue disease/vasculitis‐associated skin ulcers, third edition

The Journal of Dermatology, Volume 52, Issue 6, Page e430-e480, June 2025.
Yoshihide Asano, Jun Asai, Takayuki Ishii, Yohei Iwata, Masanari Kodera, Chie Miyabe, Akihiko Uchiyama, Youichi Ogawa, Ken Okamura, Mari Kishibe, Yuta Koike, Yorihisa Kotobuki, Noriki Fujimoto, Takuya Miyagi, Yukie Yamaguchi, Ayumi Yoshizaki, Reiko Omori, Takeshi Nakanishi, Hiroshi Fujiwara, Takeo Maekawa, Sei‐ichiro Motegi, Yuichiro Yoshino, Minoru Hasegawa, Manabu Fujimoto, Takao Tachibana, Wound, Pressure Ulcer, and Burn Guidelines Drafting Committee (connective tissue disease/vasculitis group)   +27 more
wiley   +1 more source

СИНДРОМ ЧАРДЖ-СТРОССА В СОЧЕТАНИИ С АУТОИММУННОЙ ТРОМБОЦИТОПЕНИЕЙ. 20 ЛЕТ НАБЛЮДЕНИЯ

Архивъ внутренней медицины, 2015
The description of a rare combination syndrome Churg-Strauss syndrome (CSS) with autoimmune thrombocytopenia. The disease is characterized by slow progression and refractory to standard types of immunosuppressive therapy.
Д. Л. Виноградов, Ю. Е. Виноградова   +1 more
doaj   +1 more source

Fulminant Wegener's granulomatosis: A case report [PDF]

, 2013
Introduction. Granulomatosis Wegener is anti-neutrophil cytoplasmic antibodies (ANCAs)-associated systemic vasculitis of unknown etiology. It is manifested as granulomatous necrotizing inflammation of the upper and lower parts of the respiratory tract,
Dinić Miroslav Ž., Kandolf-Sekulović Lidija, Zečević Radoš D., Zolotarevski Lidija   +3 more
core   +1 more source