Results 91 to 100 of about 27,299 (305)

Childhood polyarteritis nodosa: A rare presentation

Asian Journal of Medical Sciences, 2016
Polyarteritis nodosa (PAN) is a rare systemic vasculitis characterized by necrotizing arteritis of small to medium-sized arteries. It manifests as skin ulceration, hypertension, abdominal pain, digital gangrene, subcutaneous nodules etc.
Sandeep Lahiry
doaj   +1 more source

Giant coronary artery aneurysms in juvenile polyarteritis nodosa: a case report [PDF]

, 2012
Juvenile polyarteritis nodosa (PAN) is a rare, necrotizing vasculitis, primarily affecting small to medium-sized muscular arteries. Cardiac involvement amongst patients with PAN is uncommon and reports of coronary artery aneurysms in juvenile PAN are ...
A Gedalia, AS Al Mazyad, BH Landing, Dawn M Wahezi, DB Magilavy, DR Holsinger, EB Blau, H Maillard-Lefebvre, H Yanagawa, HJ Park, JL Chamberlain, Kanwal M Farooqi, KH Chu, M Takahashi, MA Yamazaki-Nakashimada, ML Schrader, N Gunal, N Tanaka, Norman T Ilowite, RE Ettlinger, Robert H Pass, S Bowyer, S Glanz, S Ozen, S Ozen, S Ozen, Therese L Canares, Y Sugahara   +27 more
core   +4 more sources

Drug‐Induced Renal Vasculitis: Etiology, Pathogenesis, Clinical Manifestations, and Therapeutic Approaches—A Narrative Review

Health Science Reports, Volume 8, Issue 4, April 2025.
ABSTRACT Background and Aims Drug‐induced renal vasculitis arises from various medications that cause immunological dysregulation or direct vascular damage, leading to inflammation and thrombosis. Clinical manifestations vary widely, from mild constitutional symptoms to severe organ dysfunction. This review aims to thoroughly explore drug‐induced renal
Hashim Mohamed Siraj, Masab Ali, Sampda Sanjaykumar Sharma, Afreen Begum, Muhammad Husnain Ahmad, Muhammad Hassan, Roba Kamaleldin Moustafa Kamel Aref Elsayed, Muhammad Hamza Tahir   +7 more
wiley   +1 more source

Polyarteritis nodosa: decreasing incidence in Poland

Archives of medical science : AMS, 2017
Introduction There are many studies on the epidemiology of the orphan disease polyarteritis nodosa (PAN) in European countries. The use of a hospital morbidity database is an important element of epidemiological analysis.
Krzysztof Kanecki, A. Nitsch-Osuch, P. Goryński, W. Wierzba, Patryk Tarka, P. Tyszko   +5 more
semanticscholar   +1 more source

Поражение почек при узелковом полиартериите [PDF]

, 2017
Представлены результаты исследования, которые свидетельствуют о том, что поражение почек наблюдается у 62 % больных узелковым полиартериитом, причем в 42 % случаев оно сопровождается почечной недостаточностью, зависит от пола и возраста пациентов ...
Бевзенко, Т.Б.
core  

Inner Ear Immunity and Audio‐Vestibular Dysfunction

Sensory Neuroscience, Volume 1, Issue 1, April 2025.
Diagram of the immune response of the inner ear and associated damage. ABSTRACT The inner ear is a critical sensory organ regulated by the immune system to maintain balance and respond to external stimuli. Immune cells like macrophages, lymphocytes, neutrophils, and natural killer cells play important roles in inner ear immunity. Inflammatory mediators,
Xiaofei Li, Hanyue Wang, Jing Wang, Maoli Duan, Yafeng Lyu   +4 more
wiley   +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

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

Polyarteritis nodosa presenting as peripheral vascular disease and acute limb ischemia

Journal of Postgraduate Medicine, 2017
Acute limb ischemia and peripheral vascular disease (PVD) are unusual presentations of polyarteritis nodosa (PAN). Here, we present a case with PVD of both lower limbs leading to foot claudication.
A. Shukla, A. Aggarwal
semanticscholar   +1 more source

Cutaneous polyarteritis nodosa treated with pentoxifylline and clobetasol propionate: A case report

Saudi Journal of Medicine and Medical Sciences, 2018
Cutaneous polyarteritis nodosa (cPAN) is a rare type of cutaneous vasculitis. It affects the small- and medium-sized arteries of the dermis and subcutaneous tissue without extracutaneous involvement.
Nada Abdulaziz A. Alquorain, Abdullah Salih H. Aljabr, Nada Juman Alghamdi   +2 more
doaj   +1 more source